Solomon H Snyder

Summary

Affiliation: Johns Hopkins University
Country: USA

Publications

  1. pmc H2S as a physiologic vasorelaxant: hypertension in mice with deletion of cystathionine gamma-lyase
    Guangdong Yang
    Department of Physiology, University of Saskatchewan, Saskatoon, SK S7N 5E5, Canada
    Science 322:587-90. 2008
  2. doi request reprint Neurotransmitters, receptors, and second messengers galore in 40 years
    Solomon H Snyder
    Department of Neuroscience, Johns Hopkins University, Baltimore, Maryland 21205, USA
    J Neurosci 29:12717-21. 2009
  3. ncbi request reprint Bilirubin benefits: cellular protection by a biliverdin reductase antioxidant cycle
    Thomas W Sedlak
    Department of Neuroscience, Johns Hopkins School of Medicine, Baltimore, Maryland 21205, USA
    Pediatrics 113:1776-82. 2004
  4. ncbi request reprint Obituary: Julius Axelrod (1912-2004)
    Solomon H Snyder
    Solomon H Snyder is in the Department of Neuroscience, Johns Hopkins Medical School, 725 North Wolfe Street, Baltimore, Maryland 21205, USA E mail
    Nature 433:593. 2005
  5. ncbi request reprint Forty years of neurotransmitters: a personal account
    Solomon H Snyder
    Department of Neuroscience, Johns Hopkins University School of Medicine, 725 N Wolfe St, Baltimore, MD 21205, USA
    Arch Gen Psychiatry 59:983-94. 2002
  6. pmc GOSPEL: a neuroprotective protein that binds to GAPDH upon S-nitrosylation
    Nilkantha Sen
    Solomon H Snyder Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA
    Neuron 63:81-91. 2009
  7. pmc NMDA receptor-nitric oxide transmission mediates neuronal iron homeostasis via the GTPase Dexras1
    Jaime H Cheah
    Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205, USA
    Neuron 51:431-40. 2006
  8. ncbi request reprint S-nitrosylated GAPDH initiates apoptotic cell death by nuclear translocation following Siah1 binding
    Makoto R Hara
    Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA
    Nat Cell Biol 7:665-74. 2005
  9. pmc Serine racemase deletion protects against cerebral ischemia and excitotoxicity
    Asif K Mustafa
    Solomon H Snyder Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205, USA
    J Neurosci 30:1413-6. 2010
  10. pmc S-nitrosylation/activation of COX-2 mediates NMDA neurotoxicity
    Jing Tian
    Solomon H Snyder Department of Neuroscience, Johns Hopkins University School of Medicine, 725 North Wolfe Street, Baltimore, MD 21205, USA
    Proc Natl Acad Sci U S A 105:10537-40. 2008

Detail Information

Publications101 found, 100 shown here

  1. pmc H2S as a physiologic vasorelaxant: hypertension in mice with deletion of cystathionine gamma-lyase
    Guangdong Yang
    Department of Physiology, University of Saskatchewan, Saskatoon, SK S7N 5E5, Canada
    Science 322:587-90. 2008
    ..These findings provide direct evidence that H2S is a physiologic vasodilator and regulator of blood pressure...
  2. doi request reprint Neurotransmitters, receptors, and second messengers galore in 40 years
    Solomon H Snyder
    Department of Neuroscience, Johns Hopkins University, Baltimore, Maryland 21205, USA
    J Neurosci 29:12717-21. 2009
    ..This essay highlights a selected group of particular notable discoveries, emphasizing seminal findings that have transformed thinking in the field...
  3. ncbi request reprint Bilirubin benefits: cellular protection by a biliverdin reductase antioxidant cycle
    Thomas W Sedlak
    Department of Neuroscience, Johns Hopkins School of Medicine, Baltimore, Maryland 21205, USA
    Pediatrics 113:1776-82. 2004
  4. ncbi request reprint Obituary: Julius Axelrod (1912-2004)
    Solomon H Snyder
    Solomon H Snyder is in the Department of Neuroscience, Johns Hopkins Medical School, 725 North Wolfe Street, Baltimore, Maryland 21205, USA E mail
    Nature 433:593. 2005
  5. ncbi request reprint Forty years of neurotransmitters: a personal account
    Solomon H Snyder
    Department of Neuroscience, Johns Hopkins University School of Medicine, 725 N Wolfe St, Baltimore, MD 21205, USA
    Arch Gen Psychiatry 59:983-94. 2002
    ..It is likely that totally new classes of therapeutic agents will emerge based on these transmitter molecules...
  6. pmc GOSPEL: a neuroprotective protein that binds to GAPDH upon S-nitrosylation
    Nilkantha Sen
    Solomon H Snyder Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA
    Neuron 63:81-91. 2009
    ..In intact mice, virally delivered GOSPEL selectively diminishes NMDA neurotoxicity. Thus, GOSPEL may physiologically regulate the viability of neurons and other cells...
  7. pmc NMDA receptor-nitric oxide transmission mediates neuronal iron homeostasis via the GTPase Dexras1
    Jaime H Cheah
    Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205, USA
    Neuron 51:431-40. 2006
    ..As selective iron chelation prevents NMDA neurotoxicity in cortical cultures, the NMDA-NO-Dexras1-PAP7-DMT1-iron uptake signaling cascade also appears to mediate NMDA neurotoxicity...
  8. ncbi request reprint S-nitrosylated GAPDH initiates apoptotic cell death by nuclear translocation following Siah1 binding
    Makoto R Hara
    Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA
    Nat Cell Biol 7:665-74. 2005
    ..The NO-S-nitrosylation-GAPDH-Siah1 cascade may represent an important molecular mechanism of cytotoxicity...
  9. pmc Serine racemase deletion protects against cerebral ischemia and excitotoxicity
    Asif K Mustafa
    Solomon H Snyder Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205, USA
    J Neurosci 30:1413-6. 2010
    ..Infarct volume following middle cerebral artery occlusion is dramatically diminished in several regions of the brains of SR mutant mice despite evidence of increased NMDA receptor number and sensitivity...
  10. pmc S-nitrosylation/activation of COX-2 mediates NMDA neurotoxicity
    Jing Tian
    Solomon H Snyder Department of Neuroscience, Johns Hopkins University School of Medicine, 725 North Wolfe Street, Baltimore, MD 21205, USA
    Proc Natl Acad Sci U S A 105:10537-40. 2008
    ..nNOS, via its PDZ domain, binds COX-2 with the generated NO S-nitrosylating and activating the enzyme. Selective disruption of nNOS-COX-2 binding prevents NMDA neurotoxicity...
  11. pmc Mutant huntingtin: nuclear translocation and cytotoxicity mediated by GAPDH
    Byoung Il Bae
    Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA
    Proc Natl Acad Sci U S A 103:3405-9. 2006
    ..Depletion of GAPDH or Siah1 by RNA interference diminishes nuclear translocation of mHtt...
  12. ncbi request reprint S-nitrosylation of N-ethylmaleimide sensitive factor mediates surface expression of AMPA receptors
    Yunfei Huang
    Department of Neuroscience, Johns Hopkins University, School of Medicine, 725 North Wolfe Street, Baltimore, Maryland 21205, USA
    Neuron 46:533-40. 2005
    ....
  13. pmc Nitric oxide-induced nuclear GAPDH activates p300/CBP and mediates apoptosis
    Nilkantha Sen
    Solomon H Snyder Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA
    Nat Cell Biol 10:866-73. 2008
    ..Our findings reveal a pathway in which NO-induced nuclear GAPDH mediates cell death through p300/CBP...
  14. pmc RACK1 binds to inositol 1,4,5-trisphosphate receptors and mediates Ca2+ release
    Randen L Patterson
    Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA
    Proc Natl Acad Sci U S A 101:2328-32. 2004
    ..These findings establish RACK1 as a physiologic mediator of agonist-induced Ca2+ release...
  15. pmc Modulation of D-serine levels in brains of mice lacking PICK1
    Takatoshi Hikida
    Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, MD 21287, USA
    Biol Psychiatry 63:997-1000. 2008
    ..D-serine is an endogenous coagonist of the N-methyl-D-aspartate subtype glutamate receptor. Genetic association studies have implicated genes coding for enzymes associated with D-serine metabolism in schizophrenia and bipolar disorder...
  16. pmc Rhes, a striatal-enriched small G protein, mediates mTOR signaling and L-DOPA-induced dyskinesia
    Srinivasa Subramaniam
    The Solomon H Snyder Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA
    Nat Neurosci 15:191-3. 2012
    ..Moreover, Rhes(-/-) mice showed reduced striatal mTOR signaling and diminished dyskinesia, but maintained motor improvement on L-DOPA treatment, suggesting a therapeutic benefit for Rhes-binding drugs...
  17. pmc Inositol 1,4,5-trisphosphate receptor/GAPDH complex augments Ca2+ release via locally derived NADH
    Randen L Patterson
    Department of Neuroscience, The Johns Hopkins University School of Medicine, 725 North Wolfe Street, Baltimore, MD 21205, USA
    Proc Natl Acad Sci U S A 102:1357-9. 2005
    ..Thus, the IP3R/GAPDH interaction likely enables cellular energy dynamics to impact calcium signaling...
  18. ncbi request reprint p53 mediates cellular dysfunction and behavioral abnormalities in Huntington's disease
    Byoung Il Bae
    Department of Neuroscience, Johns Hopkins University School of Medicine, 725 North Wolfe Street, Baltimore, MD 21205, USA
    Neuron 47:29-41. 2005
    ..Genetic deletion of p53 suppresses neurodegeneration in mHtt-Tg flies and neurobehavioral abnormalities of mHtt-Tg mice. Our findings suggest that p53 links nuclear and mitochondrial pathologies characteristic of HD...
  19. pmc Amino acid signaling to mTOR mediated by inositol polyphosphate multikinase
    Seyun Kim
    The Solomon H Snyder Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA
    Cell Metab 13:215-21. 2011
    ..Substances that block IPMK-mTORC1 binding may afford therapeutic benefit in nutrient amino acid-regulated conditions such as obesity and diabetes...
  20. pmc Casein kinase-2 mediates cell survival through phosphorylation and degradation of inositol hexakisphosphate kinase-2
    Anutosh Chakraborty
    The Solomon H Snyder Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA
    Proc Natl Acad Sci U S A 108:2205-9. 2011
    ..CK2 phosphorylation at the degradation motif of IP6K2 enhances its ubiquitination and subsequent degradation. IP6K2 mutants at the CK2 sites that are resistant to CK2 phosphorylation are metabolically stable...
  21. pmc HSP90 regulates cell survival via inositol hexakisphosphate kinase-2
    Anutosh Chakraborty
    The Solomon H Snyder Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA
    Proc Natl Acad Sci U S A 105:1134-9. 2008
    ..Thus, the prosurvival actions of HSP90 reflect the inhibition of IP6K2, suggesting that selectively blocking this interaction could provide effective and safer modes of chemotherapy...
  22. pmc GAPDH mediates nitrosylation of nuclear proteins
    Michael D Kornberg
    Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA
    Nat Cell Biol 12:1094-100. 2010
    ..Our findings reveal a novel mechanism for targeted nitrosylation of nuclear proteins and suggest that protein-protein transfer of nitric oxide groups may be a general mechanism in cellular signal transduction...
  23. ncbi request reprint Huntingtin is cleaved by caspases in the cytoplasm and translocated to the nucleus via perinuclear sites in Huntington's disease patient lymphoblasts
    Akira Sawa
    Department of Psychiatry and Behavioral Sciences, Johns Hopkins University School of Medicine, 600 North Wolfe Street, Baltimore, MD 21287, USA
    Neurobiol Dis 20:267-74. 2005
    ..Our findings suggest that caspase cleavage of Htt is cytoplasmic and precedes sorting to specific perinuclear sites followed by nuclear translocation in HD patient tissue...
  24. pmc A peptide inhibitor of cytochrome c/inositol 1,4,5-trisphosphate receptor binding blocks intrinsic and extrinsic cell death pathways
    Darren Boehning
    Department of Neuroscience, The Johns Hopkins University School of Medicine, 725 North Wolfe Street, Baltimore, MD 21205, USA
    Proc Natl Acad Sci U S A 102:1466-71. 2005
    ..Small-molecule inhibitors of cytochrome c/IP3R interactions may prove useful in treating disorders associated with inappropriate intrinsic and extrinsic apoptotic signaling...
  25. pmc Inositol polyphosphate multikinase is a nuclear PI3-kinase with transcriptional regulatory activity
    Adam C Resnick
    Department of Neuroscience, Johns Hopkins University School of Medicine, 725 North Wolfe Street, Baltimore, MD 21205, USA
    Proc Natl Acad Sci U S A 102:12783-8. 2005
    ..In yeast, this inositol lipid kinase activity physiologically regulates transcription...
  26. ncbi request reprint Action of TFII-I outside the nucleus as an inhibitor of agonist-induced calcium entry
    Gabriela Caraveo
    Department of Molecular Biology and Genetics, Institute for Cell Engineering, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA
    Science 314:122-5. 2006
    ..Our observations suggest a model in which TFII-I suppresses ACE by competing with TRPC3 for binding to PLC-g...
  27. pmc Glutamatergic regulation of serine racemase via reversal of PIP2 inhibition
    Asif K Mustafa
    Solomon H Snyder Department of Neuroscience, Johns Hopkins University School of Medicine, 725 North Wolfe Street, Baltimore, MD 21205, USA
    Proc Natl Acad Sci U S A 106:2921-6. 2009
    ..Thus mutants of SR that cannot bind PIP2 lose their membrane localizations and display a 4-fold enhancement of catalytic activity. Moreover, mGluR5 activation of SR activity is abolished by inhibiting phospholipase C...
  28. pmc Neuroprotection by pharmacologic blockade of the GAPDH death cascade
    Makoto R Hara
    Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA
    Proc Natl Acad Sci U S A 103:3887-9. 2006
    ..In mice treated with the dopamine neuronal toxin 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP), low doses of deprenyl prevent binding of GAPDH and Siah1 in the dopamine-enriched corpus striatum...
  29. pmc S-nitrosylation of AMPA receptor GluA1 regulates phosphorylation, single-channel conductance, and endocytosis
    Balakrishnan Selvakumar
    Solomon H Snyder Department of Neuroscience and Departments of Psychiatry and Behavioral Sciences, Pharmacology and Molecular Sciences, and Howard Hughes Medical Institute, The Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA
    Proc Natl Acad Sci U S A 110:1077-82. 2013
    ....
  30. ncbi request reprint Phospholipase Cgamma1 controls surface expression of TRPC3 through an intermolecular PH domain
    Damian B van Rossum
    Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205, USA
    Nature 434:99-104. 2005
    ..Our findings imply a far greater abundance of PH domains than previously appreciated, and suggest that intermolecular PH-like domains represent a widespread signalling mode...
  31. pmc Rhes, a striatal specific protein, mediates mutant-huntingtin cytotoxicity
    Srinivasa Subramaniam
    Solomon H Snyder Department of Neuroscience, Johns Hopkins University School of Medicine, 725 North Wolfe Street, Baltimore, MD 21205, USA
    Science 324:1327-30. 2009
    ..Using cultured cells, we found Rhes induces sumoylation of mHtt, which leads to cytotoxicity. Thus, Rhes-mHtt interactions can account for the localized neuropathology of HD...
  32. pmc Bilirubin and glutathione have complementary antioxidant and cytoprotective roles
    Thomas W Sedlak
    Department of Psychiatry and Behavioral Sciences, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA
    Proc Natl Acad Sci U S A 106:5171-6. 2009
    ..RNA interference depletion of BVR increases oxidation of lipids more than protein. Depletion of BVR or GSH augments cell death in an oxidant-specific fashion...
  33. pmc Protein pyrophosphorylation by inositol pyrophosphates is a posttranslational event
    Rashna Bhandari
    The Solomon H Snyder Department of Neuroscience, Johns Hopkins University School of Medicine, 725 North Wolfe Street, Baltimore, MD 21205, USA
    Proc Natl Acad Sci U S A 104:15305-10. 2007
    ..Pyrophosphorylation may represent a novel mode of signaling to proteins...
  34. ncbi request reprint Heme oxygenase-2 is activated by calcium-calmodulin
    Darren Boehning
    Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205, USA
    J Biol Chem 279:30927-30. 2004
    ..Calcium-calmodulin provides a mechanism for rapid and transient activation of HO2 during neuronal activity...
  35. pmc Nitric oxide S-nitrosylates serine racemase, mediating feedback inhibition of D-serine formation
    Asif K Mustafa
    Solomon H Snyder Department of Neuroscience, The Johns Hopkins University School of Medicine, 725 North Wolfe Street, Baltimore, MD 21205, USA
    Proc Natl Acad Sci U S A 104:2950-5. 2007
    ..These findings support a model whereby postsynaptic stimulation of nitric-oxide (NO) formation feeds back to presynaptic cells to S-nitrosylate SR and decrease D-serine availability to postsynaptic NMDA receptors...
  36. pmc Inositol pyrophosphates inhibit Akt signaling, thereby regulating insulin sensitivity and weight gain
    Anutosh Chakraborty
    The Solomon H Snyder Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA
    Cell 143:897-910. 2010
    ..IP6K1 knockout mice manifest insulin sensitivity and are resistant to obesity elicited by high-fat diet or aging. Inhibition of IP6K1 may afford a therapeutic approach to obesity and diabetes...
  37. pmc Rhes, a physiologic regulator of sumoylation, enhances cross-sumoylation between the basic sumoylation enzymes E1 and Ubc9
    Srinivasa Subramaniam
    Solomon H Snyder Department of Neuroscience, Departments of Pharmacology and Molecular Sciences and Psychiatry, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA
    J Biol Chem 285:20428-32. 2010
    ..quot; Rhes binds directly to both E1 and Ubc9, enhancing cross-sumoylation as well as thioester transfer from E1 to Ubc9...
  38. pmc p53-mediated apoptosis requires inositol hexakisphosphate kinase-2
    Michael A Koldobskiy
    The Solomon H Snyder Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA
    Proc Natl Acad Sci U S A 107:20947-51. 2010
    ..IP6K2 acts by binding directly to p53 and decreasing expression of proarrest gene targets such as the cyclin-dependent kinase inhibitor p21...
  39. ncbi request reprint A nitric oxide signaling pathway controls CREB-mediated gene expression in neurons
    Antonella Riccio
    Howard Hughes Medical Institute, The Johns Hopkins University School of Medicine, 725 North Wolfe Street, Baltimore, Maryland 21201, USA
    Mol Cell 21:283-94. 2006
    ..Thus, in conjunction with CREB phosphorylation, the NO pathway controls CREB-DNA binding and CRE-mediated gene expression...
  40. pmc Death-associated protein kinase-mediated cell death modulated by interaction with DANGER
    Bingnan N Kang
    Department of Pharmacology and Molecular Sciences, The Johns Hopkins University School of Medicine, Baltimore, Maryland 21205, USA
    J Neurosci 30:93-8. 2010
    ..Accordingly, DANGER may physiologically regulate the viability of neurons and represent a potential therapeutic target for stroke and neurodegenerative diseases...
  41. ncbi request reprint Inositol hexakisphosphate kinase-2, a physiologic mediator of cell death
    Eiichiro Nagata
    Department of Neuroscience, Pharmacology and Molecular Sciences, School of Medicine, The Johns Hopkins University, Baltimore, Maryland 21205, USA
    J Biol Chem 280:1634-40. 2005
    ..The present study provides compelling evidence that endogenous InsP6K2, by generating InsP7, provides physiologic regulation of the apoptotic process...
  42. pmc Aspartate racemase, generating neuronal D-aspartate, regulates adult neurogenesis
    Paul M Kim
    The Solomon H Snyder Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA
    Proc Natl Acad Sci U S A 107:3175-9. 2010
    ..Because D-aspartate is a potential endogenous ligand for NMDA receptors, the loss of which elicits a phenotype resembling DR depletion, D-aspartate may function as a modulator of adult neurogenesis...
  43. pmc Hydrogen sulfide as endothelium-derived hyperpolarizing factor sulfhydrates potassium channels
    Asif K Mustafa
    Solomon H Snyder Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA
    Circ Res 109:1259-68. 2011
    ..Hydrogen sulfide (H(2)S) is a prominent EDRF, since mice lacking its biosynthetic enzyme, cystathionine γ-lyase (CSE), display pronounced hypertension with deficient vasorelaxant responses to acetylcholine...
  44. pmc Hydrogen sulfide-linked sulfhydration of NF-κB mediates its antiapoptotic actions
    Nilkantha Sen
    The Solomon H Snyder Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA
    Mol Cell 45:13-24. 2012
    ..In CSE mutant mice, antiapoptotic influences of NF-κB are markedly diminished. Thus, sulfhydration of NF-κB appears to be a physiologic determinant of its antiapoptotic transcriptional activity...
  45. pmc Neurotrophin-mediated degradation of histone methyltransferase by S-nitrosylation cascade regulates neuronal differentiation
    Nilkantha Sen
    The Solomon H Snyder Department of Neuroscience, The Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA
    Proc Natl Acad Sci U S A 108:20178-83. 2011
    ..Degradation of SUV39H1 by Siah facilitates histone H3 on lysine 9 acetylation, CREB binding to DNA, enhanced expression of CREB-regulated genes and neurite outgrowth...
  46. pmc Serine racemase: activation by glutamate neurotransmission via glutamate receptor interacting protein and mediation of neuronal migration
    Paul M Kim
    Department of Pharmacology and Molecular Science, Neuroscience, The Johns Hopkins University School of Medicine, 725 North Wolfe Street, Baltimore, MD 21205, USA
    Proc Natl Acad Sci U S A 102:2105-10. 2005
    ..Thus, in neuronal migration, glutamate stimulates Bergmann glia to form and release D-serine, which, together with glutamate, activates NMDA receptors on granule neurons, chemokinetically enhancing migration...
  47. pmc H2S signals through protein S-sulfhydration
    Asif K Mustafa
    Solomon H Snyder Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA
    Sci Signal 2:ra72. 2009
    ..Sulfhydration augments GAPDH activity and enhances actin polymerization. Sulfhydration thus appears to be a physiologic posttranslational modification for proteins...
  48. pmc Agonist-induced Ca2+ entry determined by inositol 1,4,5-trisphosphate recognition
    Damian B van Rossum
    Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA
    Proc Natl Acad Sci U S A 101:2323-7. 2004
    ..We conclude that an IP3-dependent conformational change in the IP3R, not endoplasmic reticulum Ca2+ pool release, triggers ACE...
  49. doi request reprint Glutathione is a physiologic reservoir of neuronal glutamate
    Minori Koga
    Department of Psychiatry and Behavioral Sciences, The Johns Hopkins University School of Medicine, Meyer 4 137, 600 North Wolfe Street, Baltimore, MD 21287, USA
    Biochem Biophys Res Commun 409:596-602. 2011
    ..Increased glutamate levels following inhibition of glutathione synthesis temporally precede later effects upon oxidative stress...
  50. pmc Inositol pyrophosphates regulate cell death and telomere length through phosphoinositide 3-kinase-related protein kinases
    Adolfo Saiardi
    Department of Neuroscience, Pharmacology and Molecular Sciences, and Psychiatry and Behavioral Sciences, The Johns Hopkins University School of Medicine, 725 North Wolfe Street, Baltimore, MD 21205, USA
    Proc Natl Acad Sci U S A 102:1911-4. 2005
    ....
  51. pmc S-nitrosylation of stargazin regulates surface expression of AMPA-glutamate neurotransmitter receptors
    Balakrishnan Selvakumar
    Solomon H Snyder Department of Neuroscience, Johns Hopkins University School of Medicine, 725 North Wolfe Street, Baltimore, MD 21205, USA
    Proc Natl Acad Sci U S A 106:16440-5. 2009
    ..NMDAR stimulation, well known to activate neuronal nitric oxide synthase, increases both nitrosylation of stargazin and its binding to AMPAR. Thus, S-nitrosylation of stargazin is a physiologic regulator of AMPAR surface expression...
  52. ncbi request reprint Nitric oxide-GAPDH-Siah: a novel cell death cascade
    Makoto R Hara
    The Solomon H Snyder Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA
    Cell Mol Neurobiol 26:527-38. 2006
    ..The neuroprotective actions of the monoamine oxidase inhibitor R-(-)-deprenyl (deprenyl) reflect blockade of GAPDH-Siah binding. Thus, novel cytoprotective therapies may emerge from agents that prevent GAPDH-Siah binding...
  53. ncbi request reprint Neuroscience. Adam finds an exciting mate
    Solomon H Snyder
    Department of Neuroscience, Johns Hopkins University School of Medicine, 725 North Wolfe Street, Baltimore, MD 21205, USA
    Science 313:1744-5. 2006
  54. doi request reprint Inositol polyphosphate multikinase is a coactivator of p53-mediated transcription and cell death
    Risheng Xu
    Department of Pharmacology and Molecular Sciences, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA
    Sci Signal 6:ra22. 2013
    ..These results suggest that IPMK acts as a transcriptional coactivator for p53 and that it is an integral part of the p53 transcriptional complex facilitating cell death...
  55. ncbi request reprint Cell signaling and neuronal death
    Makoto R Hara
    The Solomon H Snyder Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA
    Annu Rev Pharmacol Toxicol 47:117-41. 2007
    ..Within cells, calcium, the most prominent of all intracellular messengers, mediates diverse forms of cell death with actions modulated by many proteins, including IP3 receptors, calcineurin, calpain, and cytochrome c...
  56. pmc S-nitrosylation and S-palmitoylation reciprocally regulate synaptic targeting of PSD-95
    Gary P H Ho
    Solomon H Snyder Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA
    Neuron 71:131-41. 2011
    ..Thus, differential modification of cysteines may represent a general paradigm in signal transduction...
  57. ncbi request reprint Phosphorylation of proteins by inositol pyrophosphates
    Adolfo Saiardi
    Department of Neuroscience, Johns Hopkins University, School of Medicine, 725 North Wolfe Street, Baltimore, MD 21205, USA
    Science 306:2101-5. 2004
    ..We also observed phosphorylation of endogenous proteins by endogenous IP7 in yeast. Phosphorylation by IP7 is nonenzymatic and may represent a novel intracellular signaling mechanism...
  58. pmc Neuronal growth and survival mediated by eIF5A, a polyamine-modified translation initiation factor
    Yunfei Huang
    Solomon H Snyder Department of Neuroscience, Johns Hopkins University School of Medicine, 725 North Wolfe Street, Baltimore, MD 21205, USA
    Proc Natl Acad Sci U S A 104:4194-9. 2007
    ..In brain cultures, inhibition of hypusine formation also inhibits neuronal process extension...
  59. pmc Inositol polyphosphate multikinase is a physiologic PI3-kinase that activates Akt/PKB
    David Maag
    The Solomon H Snyder Department of Neuroscience, The Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA
    Proc Natl Acad Sci U S A 108:1391-6. 2011
    ..Drugs regulating IPMK may have therapeutic relevance in influencing cell proliferation...
  60. ncbi request reprint The cationic amino acid transporters CAT1 and CAT3 mediate NMDA receptor activation-dependent changes in elaboration of neuronal processes via the mammalian target of rapamycin mTOR pathway
    Yunfei Huang
    Solomon H Snyder Department of Neuroscience, Johns Hopkins University, School of Medicine, Baltimore, Maryland 21205, USA
    J Neurosci 27:449-58. 2007
    ..Thus, the CATs mediate influences of NMDA receptor activation on the mTOR pathway that regulates neuronal processes...
  61. pmc Gene deletion of inositol hexakisphosphate kinase 1 reveals inositol pyrophosphate regulation of insulin secretion, growth, and spermiogenesis
    Rashna Bhandari
    The Solomon H Snyder Department of Neuroscience and Departments of Pharmacology and Molecular Sciences and Psychiatry and Behavioral Sciences, Johns Hopkins University School of Medicine, 725 North Wolfe Street, Baltimore, MD 21205, USA
    Proc Natl Acad Sci U S A 105:2349-53. 2008
    ..Male mutant mice are sterile with defects in spermiogenesis. Mutant mice are smaller than wild-type despite normal food intake. The mutants display markedly lower circulating insulin...
  62. ncbi request reprint Genetics. Two genes link two distinct psychoses
    Akira Sawa
    Department of Psychiatry, Johns Hopkins University School of Medicine, 725 North Wolfe Street, Baltimore, MD 21205, USA
    Science 310:1128-9. 2005
  63. ncbi request reprint D-aspartate regulates melanocortin formation and function: behavioral alterations in D-aspartate oxidase-deficient mice
    Alex S Huang
    Department of Neuroscience, The Johns Hopkins University School of Medicine, Baltimore, Maryland 21205, USA
    J Neurosci 26:2814-9. 2006
    ..Therefore, Ddo is the endogenous enzyme that degrades D-aspartate, and Ddo-enriched organs, low in D-aspartate, may represent areas of high turnover where D-aspartate may be physiologically important...
  64. ncbi request reprint Messenger molecules and cell death: therapeutic implications
    Thomas W Sedlak
    Department of Neuroscience, Johns Hopkins School of Medicine, Baltimore, MD 21205, USA
    JAMA 295:81-9. 2006
    ..These pathways may regulate cell survival in a variety of pathologic states and represent fertile targets for novel therapies...
  65. ncbi request reprint Inducible nitric oxide synthase binds, S-nitrosylates, and activates cyclooxygenase-2
    Sangwon F Kim
    Department of Neuroscience, Johns Hopkins University School of Medicine, 725 North Wolfe Street, Baltimore, MD 21205, USA
    Science 310:1966-70. 2005
    ..Selectively disrupting iNOS-COX-2 binding prevented NO-mediated activation of COX-2. This synergistic molecular interaction between two inflammatory systems may inform the development of anti-inflammatory drugs...
  66. pmc Biliverdin reductase: a major physiologic cytoprotectant
    David E Baranano
    Departments of Neuroscience, Pharmacology and Molecular Sciences, and Psychiatry and Behavioral Sciences, The Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA
    Proc Natl Acad Sci U S A 99:16093-8. 2002
    ..This redox cycle may constitute the principal physiologic function of bilirubin...
  67. pmc Alternatively spliced neuronal nitric oxide synthase mediates penile erection
    K Joseph Hurt
    Department of Urology, Division of Cardiology, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA
    Proc Natl Acad Sci U S A 103:3440-3. 2006
    ..Thus, alternatively spliced forms of nNOS are major mediators of penile erection and so may be targets for therapeutic intervention...
  68. pmc Carbon monoxide mediates vasoactive intestinal polypeptide-associated nonadrenergic/noncholinergic neurotransmission
    Crystal C Watkins
    Department of Neuroscience, The Johns Hopkins University School of Medicine, 725 North Wolfe Street, Baltimore, MD 21205, USA
    Proc Natl Acad Sci U S A 101:2631-5. 2004
    ..By using a combination of pharmacology and genetic knockout of the biosynthetic enzymes for CO and NO, we show that the physiologic effects of exogenous and endogenous VIP in the IAS are mediated by HO2-synthesized CO...
  69. ncbi request reprint Circadian rhythms. Carbon monoxide and clocks
    Darren Boehning
    Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA
    Science 298:2339-40. 2002
  70. doi request reprint Molecules of madness
    Solomon H Snyder
    The Solomon H Snyder Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA
    Cell 139:1212-5. 2009
    ..Hopefully, the tale of my quirky impatient curiosity about "too many" different areas will be useful for young scientists embarking on their own careers...
  71. ncbi request reprint Inositol 1,4,5-trisphosphate receptors as signal integrators
    Randen L Patterson
    Department of Neuroscience, Johns Hopkins University, Johns Hopkins Medical School, Baltimore, Maryland 21205, USA
    Annu Rev Biochem 73:437-65. 2004
    ..We review the unique properties of the IP3R that facilitate cell-type and stimulus-dependent control of function, with special emphasis on protein-binding partners...
  72. ncbi request reprint Novel neural modulators
    Darren Boehning
    Department of Neuroscience, Johns Hopkins University School of Medicine, 725 N Wolfe Street, Baltimore, Maryland 21205, USA
    Annu Rev Neurosci 26:105-31. 2003
    ..We review the properties of these "atypical" neural modulators...
  73. ncbi request reprint Historical review: Opioid receptors
    Solomon H Snyder
    Johns Hopkins University School of Medicine, Department of Neuroscience, 725 N Wolfe Street, Baltimore, MD 21205, USA
    Trends Pharmacol Sci 24:198-205. 2003
    ..Receptor influences in binding paradigms and smooth muscle pharmacology permitted the identification and isolation of endogenous opioid peptides...
  74. ncbi request reprint Opiate receptors and beyond: 30 years of neural signaling research
    Solomon H Snyder
    Department of Neuroscience, Johns Hopkins University School of Medicine, 725 North Wolfe Street, WBSB 813, Baltimore, MD 21205, USA
    Neuropharmacology 47:274-85. 2004
    ..These techniques also permitted characterization of intracellular signaling systems such as the IP3 receptor and immunophilins. Even more novel than the enkephalins have been the gaseous neurotransmitters NO and CO and D-serine...
  75. ncbi request reprint Opiate receptor revisited
    Solomon H Snyder
    Department of Neuroscience, Johns Hopkins University, Baltimore, MD, USA
    Anesthesiology 107:659-61. 2007
  76. ncbi request reprint Neuroscience at Johns Hopkins
    Solomon H Snyder
    Department of Neuroscience, Johns Hopkins University School of Medicine, 725 North Wolfe Street, Baltimore, Maryland 21205, USA
    Neuron 48:201-11. 2005
  77. ncbi request reprint Turning off neurotransmitters
    Solomon H Snyder
    Department of Neuroscience, Johns Hopkins University, 725 N Wolfe Street, WBSB 813 Baltimore, MD 21205, USA
    Cell 125:13-5. 2006
    ....
  78. ncbi request reprint Carbon monoxide neurotransmission activated by CK2 phosphorylation of heme oxygenase-2
    Darren Boehning
    Department of Neuroscience, Johns Hopkins University School of Medicine, 725 North Wolfe Street, Baltimore, MD 21205, USA
    Neuron 40:129-37. 2003
    ..Our findings provide a molecular mechanism for the rapid neuronal activation of CO biosynthesis, as required for a gaseous neurotransmitter...
  79. ncbi request reprint Cytochrome c binds to inositol (1,4,5) trisphosphate receptors, amplifying calcium-dependent apoptosis
    Darren Boehning
    Department of Neuroscience, Johns Hopkins University School of Medicine, 725 N Wolfe Street, Baltimore, Maryland 21205, USA
    Nat Cell Biol 5:1051-61. 2003
    ..Our findings identify a feed-forward mechanism whereby early cytochrome c release increases InsP(3)R function, resulting in augmented cytochrome c release that amplifies the apoptotic signal...
  80. ncbi request reprint Julius Axelrod
    Solomon H Snyder
    Department of Neuroscience, Johns Hopkins University School of Medicine, USA
    Proc Am Philos Soc 151:81-90. 2007
  81. pmc Neuronal nitric-oxide synthase localization mediated by a ternary complex with synapsin and CAPON
    Samie R Jaffrey
    Department of Neuroscience, The Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA
    Proc Natl Acad Sci U S A 99:3199-204. 2002
    ..These results suggest a mechanism for specific actions of NO at presynaptic sites...
  82. ncbi request reprint Inositol pyrophosphates mediate chemotaxis in Dictyostelium via pleckstrin homology domain-PtdIns(3,4,5)P3 interactions
    Hongbo R Luo
    Department of Neuroscience, Johns Hopkins University, School of Medicine, Baltimore, MD 21205, USA
    Cell 114:559-72. 2003
    ..InsP7 competes for PH domain binding with PtdIns(3,4,5)P3 both in vitro and in vivo. InsP7 depletion enhances PH domain membrane translocation and augments downstream chemotactic signaling activity...
  83. pmc Hydrogen sulfide as a gasotransmitter
    Moataz M Gadalla
    Department of Pharmacology and Molecular Sciences, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205 2105, USA
    J Neurochem 113:14-26. 2010
    ..S-nitrosylation basally affects 1-2% of its target proteins, while 10-25% of H(2)S target proteins are S-sulfhydrated. In summary, H(2)S appears to be a physiologic gasotransmitter of comparable importance to NO and carbon monoxide...
  84. pmc Akt-dependent phosphorylation of endothelial nitric-oxide synthase mediates penile erection
    K Joseph Hurt
    Department of Neuroscience, Johns Hopkins University School of Medicine, 725 North Wolfe Street, Baltimore, MD 21205, USA
    Proc Natl Acad Sci U S A 99:4061-6. 2002
    ..Our findings support a model in which rapid, brief activation of neuronal NOS initiates the erectile process, whereas PI3-kinase/Akt-dependent phosphorylation and activation of eNOS leads to sustained NO production and maximal erection...
  85. ncbi request reprint Schizophrenia: diverse approaches to a complex disease
    Akira Sawa
    Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA
    Science 296:692-5. 2002
    ..Here, we provide a brief overview of the parallel approaches being used to identify the molecular causes of schizophrenia and discuss possible directions for future research...
  86. pmc Signaling by gasotransmitters
    Asif K Mustafa
    Solomon H Snyder Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA
    Sci Signal 2:re2. 2009
    ..This Review focuses on mechanisms whereby they signal by binding to metal centers in metalloproteins, such as in guanylyl cyclase, or modifying sulfhydryl groups in protein targets...
  87. ncbi request reprint Phospholipase C gamma 1 is a physiological guanine nucleotide exchange factor for the nuclear GTPase PIKE
    Keqiang Ye
    Johns Hopkins University School of Medicine, Department of Neuroscience, 725 N Wolfe Street, Baltimore, Maryland 21205, USA
    Nature 415:541-4. 2002
    ..This enzymatic activity accounts for the mitogenic properties of PLC-gamma 1...
  88. ncbi request reprint UDP-glucuronate decarboxylase, a key enzyme in proteoglycan synthesis: cloning, characterization, and localization
    John L Moriarity
    Department of Neurological Surgery, Johns Hopkins School of Medicine, Baltimore, Maryland 21205, USA
    J Biol Chem 277:16968-75. 2002
    ..Subcellular studies and histochemistry localized UGD protein to the perinuclear Golgi where xylosylation of proteoglycan core proteins is known to occur...
  89. pmc Schizophrenia: neural mechanisms for novel therapies
    Akira Sawa
    Department of Neuroscience, Johns Hopkins University, School of Medicine, Baltimore, MD 21205, USA
    Mol Med 9:3-9. 2003
    ..The search for genes linked to schizophrenia has revealed several leads that may permit development of novel therapeutic agents. Promising genes include disrupted-in-schizophrenia-1, dysbindin, and neuregulin...
  90. pmc Disrupted-in-Schizophrenia-1 (DISC-1): mutant truncation prevents binding to NudE-like (NUDEL) and inhibits neurite outgrowth
    Yuji Ozeki
    Division of Neurobiology and Department of Psychiatry, Johns Hopkins University School of Medicine, 600 North Wolfe Street, Baltimore, MD 21205, USA
    Proc Natl Acad Sci U S A 100:289-94. 2003
    ..As schizophrenia is thought to reflect defects in cortical development that are determined by cytoskeletal protein activities, the cellular disturbances we observe with mutant DISC-1 may be relevant to psychopathologic mechanisms...
  91. pmc From the Cover: Antipsychotic drug-induced weight gain mediated by histamine H1 receptor-linked activation of hypothalamic AMP-kinase
    Sangwon F Kim
    The Solomon H Snyder Department of Neuroscience, Departments of Pharmacology and Molecular Sciences and Psychiatry and Behavioral Sciences, The Johns Hopkins University School of Medicine, 725 North Wolfe Street, Baltimore, MD 21205, USA
    Proc Natl Acad Sci U S A 104:3456-9. 2007
    ..These findings may afford a means of developing more effective therapeutic agents and provide insight into the hypothalamic regulation of food intake...
  92. pmc Calpain-dependent cleavage of cain/cabin1 activates calcineurin to mediate calcium-triggered cell death
    Min Jung Kim
    Department of Life Science, Kwangju Institute of Science and Technology, 1 Oryong dong, Puk Gu, Kwangju 500 712, Korea
    Proc Natl Acad Sci U S A 99:9870-5. 2002
    ..Taken together, these results indicate that calpain cleaves the calcineurin-binding domain of cain/cabin1 to activate Cn and elicit calcium-triggered cell death...
  93. ncbi request reprint PI3 kinase enhancer-Homer complex couples mGluRI to PI3 kinase, preventing neuronal apoptosis
    Rong Rong
    Department of Pathology and Laboratory Medicine, Emory University School of Medicine, Room 145, Whitehead Building, 615 Michael Street, Atlanta, Georgia 30322, USA
    Nat Neurosci 6:1153-61. 2003
    ..Our findings indicate that this complex mediates the well-known ability of agonists of mGluRI to prevent neuronal apoptosis...
  94. pmc Regulation of AMPA receptor localization in lipid rafts
    Qingming Hou
    Department of Biology, Boston University, Boston, MA 02215, USA
    Mol Cell Neurosci 38:213-23. 2008
    ..Perturbation of lipid rafts dramatically suppresses AMPA receptor exocytosis, resulting in significant reduction in AMPAR cell-surface expression...
  95. ncbi request reprint DANGER, a novel regulatory protein of inositol 1,4,5-trisphosphate-receptor activity
    Damian B van Rossum
    Department of Biology, Pennsylvania State University, University Park, Pennsylvania 16802, USA
    J Biol Chem 281:37111-6. 2006
    ..DANGER appears to allosterically modulate the sensitivity of IP(3) RtoCa(2+) inhibition, which likely alters IP(3)R-mediated Ca(2+) dynamics in cells where DANGER and IP(3)R are co-expressed...
  96. ncbi request reprint No glial death with NO
    Solomon H Snyder
    Nat Cell Biol 6:17-8. 2004
  97. ncbi request reprint Phospholipase C-gamma: diverse roles in receptor-mediated calcium signaling
    Randen L Patterson
    Department of Biology, The Pennsylvania State University, Life Science Building, Shortlidge Road, University Park, PA 16801, USA
    Trends Biochem Sci 30:688-97. 2005
    ..Understanding the underlying molecular mechanisms that regulate this complex will probably clarify the processes of receptor-activated Ca2+ entry...
  98. ncbi request reprint PIKE GTPase: a novel mediator of phosphoinositide signaling
    Keqiang Ye
    Department of Pathology and Laboratory Medicine, Emory University School of Medicine, 615 Michael Street, Atlanta, GA 30322, USA
    J Cell Sci 117:155-61. 2004
    ..PIKE-L could have additional, extranuclear functions, including regulation of postsynaptic signaling by metabotropic glutamate receptors...
  99. pmc Regulation of telomere length by fatty acid elongase 3 in yeast. Involvement of inositol phosphate metabolism and Ku70/80 function
    Suriyan Ponnusamy
    Department of Biochemistry and Molecular Biology, Medical University of South Carolina, Charleston, South Carolina 29425, USA
    J Biol Chem 283:27514-24. 2008
    ....
  100. doi request reprint Neuroscience: a complex in psychosis
    Solomon H Snyder
    Nature 452:38-9. 2008
  101. ncbi request reprint The peripheral-type benzodiazepine receptor and tumorigenicity: isoquinoline binding protein (IBP) antisense knockdown in the C6 glioma cell line
    Evgeny Levin
    Rappaport Family Institute for Research in the Medical Sciences, Technion Israel Institute of Technology, Haifa, Israel
    Biochemistry 44:9924-35. 2005
    ..In conclusion, our results suggest that enhanced IBP expression, including enhanced PBR ligand binding, such as occurring in untreated C6 glioma cells, may provide a mechanism to increase apoptotic rates of cancer cells...