Jun Nakae

Summary

Affiliation: Kobe University
Country: Japan

Publications

  1. ncbi Forkhead transcription factor FoxO1 in adipose tissue regulates energy storage and expenditure
    Jun Nakae
    Department of Clinical Molecular Medicine, Division of Diabetes, Digestive and Kidney Diseases, Kobe University Graduate School of Medicine, Kobe 650 0017, Japan
    Diabetes 57:563-76. 2008
  2. ncbi The FoxO transcription factors and metabolic regulation
    Jun Nakae
    21st Century COE Program for Signal Transduction Disease, Kobe University Graduate School of Medicine, Kobe 650 0017, Japan
    FEBS Lett 582:54-67. 2008
  3. ncbi The LXXLL motif of murine forkhead transcription factor FoxO1 mediates Sirt1-dependent transcriptional activity
    Jun Nakae
    Department of Clinical Molecular Medicine, Division of Diabetes, Digestive and Kidney Disease, Kobe University Graduate School of Medicine, Kobe, Japan
    J Clin Invest 116:2473-83. 2006
  4. ncbi PDK1-Foxo1 in agouti-related peptide neurons regulates energy homeostasis by modulating food intake and energy expenditure
    Yongheng Cao
    Division of Molecular Medicine and Medical Genetics, International Center for Medical Research and Treatment, Kobe University Graduate School of Medicine, Japan
    PLoS ONE 6:e18324. 2011
  5. ncbi PDK-1/FoxO1 pathway in POMC neurons regulates Pomc expression and food intake
    Kristy Iskandar
    International Center for Medical Research and Treatment, Kobe University Graduate School of Medicine, Japan
    Am J Physiol Endocrinol Metab 298:E787-98. 2010
  6. ncbi Novel repressor regulates insulin sensitivity through interaction with Foxo1
    Jun Nakae
    Frontier Medicine on Metabolic Syndrome, Division of Endocrinology, Metabolism and Nephrology, Department of Internal Medicine, Keio University School of Medicine, Tokyo, Japan
    EMBO J 31:2275-95. 2012
  7. ncbi Muscle-specific overexpression of heparin-binding epidermal growth factor-like growth factor increases peripheral glucose disposal and insulin sensitivity
    Yasuhide Fukatsu
    Department of Clinical Molecular Medicine, Division of Diabetes, Kobe University Graduate School of Medicine, Kobe, Japan
    Endocrinology 150:2683-91. 2009
  8. ncbi Interaction of FoxO1 and TSC2 induces insulin resistance through activation of the mammalian target of rapamycin/p70 S6K pathway
    Yongheng Cao
    Department of Clinical Molecular Medicine, Division of Diabetes, Digestive and Kidney Disease, Kobe University Graduate School of Medicine, Kobe 650 0017, Japan
    J Biol Chem 281:40242-51. 2006
  9. ncbi Transgenic rescue of insulin receptor-deficient mice
    Haruka Okamoto
    Department of Medicine, Institute of Human Nutrition, College of Physicians and Surgeons, Columbia University, New York, New York, USA
    J Clin Invest 114:214-23. 2004
  10. ncbi Insulin/Foxo1 pathway regulates expression levels of adiponectin receptors and adiponectin sensitivity
    Atsushi Tsuchida
    Department of Internal Medicine, Graduate School of Medicine, University of Tokyo, Tokyo 113 8655, Japan
    J Biol Chem 279:30817-22. 2004

Collaborators

  • Masato Kasuga
  • Wataru Ogawa
  • Hiroshi Itoh
  • Atsuhiro Ichihara
  • Masanori Nakata
  • Streamson Chua
  • Hitoshi Okamura
  • Gregory S Barsh
  • Yasuhiko Minokoshi
  • Okio Hino
  • D Accili
  • Tadahiro Kitamura
  • Karen C Arden
  • C Kahn
  • T Kadowaki
  • Morris F White
  • Yongheng Cao
  • Kristy Iskandar
  • Yoshitake Hayashi
  • Tetsuo Noda
  • Eisuke Takano
  • Toshihiko Yada
  • Yasuhide Fukatsu
  • Shouhong Xuan
  • Yoshiaki Kido
  • Haruka Okamoto
  • Atsushi Tsuchida
  • Jennifer Altomonte
  • Marta L Hribal
  • Argiris Efstratiadis
  • Kenji Kangawa
  • Hiroshi Hosoda
  • Kazunori Nakajima
  • Shiki Okamoto
  • Yukio Hirata
  • Miyo Oki
  • Changliang Zhang
  • Tetsuya Noguchi
  • Kohei Kaku
  • Ko Kotani
  • Kazuo Inoue
  • Ryuji Hiramatsu
  • Masahiro Matsuo
  • Toyo Yoshioka
  • Kenjiro Inagaki
  • Kazutoshi Tobimatsu
  • Takeshi Ogura
  • Yasushi Matsuki
  • Takaya Abe
  • Mashito Sakai
  • Tetsuro Shibakusa
  • Tetsuya Hosooka
  • Tohru Fushiki
  • Toshiyuki Kobayashi
  • Yuji Kamioka
  • Norihide Yokoi
  • Masafumi Onodera
  • Naoki Mochizuki
  • Toshimasa Yamauchi
  • Yusuke Hada
  • Ryo Suzuki
  • Masaki Kobayashi
  • Byung-Chul Park
  • Kazuyuki Tobe
  • Ioannis Dragatsis
  • Byung Chul Park
  • Philippe Froguel
  • Kazuo Hara
  • Toshiyuki Maki
  • Sato Takekawa
  • Ryozo Nagai
  • Yasuo Terauchi
  • Kohjiro Ueki
  • Junji Kamon
  • Naoto Kubota
  • Yusuke Ito
  • Sonal Harbaran
  • Swan N Thung
  • Anja Richter
  • Marcia Meseck
  • John R Shutter
  • Jenny Suriawinata
  • Hengjiang Dong
  • Katerina Politi
  • Pedro L Herrera
  • Peter E Fisher
  • Marta Letizia Hribal
  • Manrico Morroni
  • Saverio Cinti

Detail Information

Publications18

  1. ncbi Forkhead transcription factor FoxO1 in adipose tissue regulates energy storage and expenditure
    Jun Nakae
    Department of Clinical Molecular Medicine, Division of Diabetes, Digestive and Kidney Diseases, Kobe University Graduate School of Medicine, Kobe 650 0017, Japan
    Diabetes 57:563-76. 2008
    ..Forkhead box-containing protein O subfamily (FoxO) 1 mediates insulin action at the transcriptional level. However, physiological roles of FoxO1 in adipose tissue remain unclear...
  2. ncbi The FoxO transcription factors and metabolic regulation
    Jun Nakae
    21st Century COE Program for Signal Transduction Disease, Kobe University Graduate School of Medicine, Kobe 650 0017, Japan
    FEBS Lett 582:54-67. 2008
    ..The understanding of molecular mechanism how FoxOs affect glucose or lipid metabolism will shed light on the novel therapy of type 2 diabetes and the metabolic syndrome...
  3. ncbi The LXXLL motif of murine forkhead transcription factor FoxO1 mediates Sirt1-dependent transcriptional activity
    Jun Nakae
    Department of Clinical Molecular Medicine, Division of Diabetes, Digestive and Kidney Disease, Kobe University Graduate School of Medicine, Kobe, Japan
    J Clin Invest 116:2473-83. 2006
    ..In conclusion, the LXXLL motif of FoxO1 may have an important role for its transcriptional activity and Sirt1 binding and should be a target site for regulation of gene expression of FoxO1 target genes and glucose metabolism in vivo...
  4. ncbi PDK1-Foxo1 in agouti-related peptide neurons regulates energy homeostasis by modulating food intake and energy expenditure
    Yongheng Cao
    Division of Molecular Medicine and Medical Genetics, International Center for Medical Research and Treatment, Kobe University Graduate School of Medicine, Japan
    PLoS ONE 6:e18324. 2011
    ..These results suggested that PDK1 and Foxo1 signaling pathways play important roles in the control of energy homeostasis through AGRP-independent mechanisms...
  5. ncbi PDK-1/FoxO1 pathway in POMC neurons regulates Pomc expression and food intake
    Kristy Iskandar
    International Center for Medical Research and Treatment, Kobe University Graduate School of Medicine, Japan
    Am J Physiol Endocrinol Metab 298:E787-98. 2010
    ..These data suggest a requirement for PDK-1 and FoxO1 in transcriptional regulation of Pomc and food intake...
  6. ncbi Novel repressor regulates insulin sensitivity through interaction with Foxo1
    Jun Nakae
    Frontier Medicine on Metabolic Syndrome, Division of Endocrinology, Metabolism and Nephrology, Department of Internal Medicine, Keio University School of Medicine, Tokyo, Japan
    EMBO J 31:2275-95. 2012
    ..Taken together, these data suggest that FCoR is a novel repressor that regulates insulin sensitivity and energy metabolism in adipose tissue by acting to fine-tune Foxo1 activity...
  7. ncbi Muscle-specific overexpression of heparin-binding epidermal growth factor-like growth factor increases peripheral glucose disposal and insulin sensitivity
    Yasuhide Fukatsu
    Department of Clinical Molecular Medicine, Division of Diabetes, Kobe University Graduate School of Medicine, Kobe, Japan
    Endocrinology 150:2683-91. 2009
    ..Our results suggest that HB-EGF produced by contracting muscle acts as an insulin sensitizer that facilitates peripheral glucose disposal...
  8. ncbi Interaction of FoxO1 and TSC2 induces insulin resistance through activation of the mammalian target of rapamycin/p70 S6K pathway
    Yongheng Cao
    Department of Clinical Molecular Medicine, Division of Diabetes, Digestive and Kidney Disease, Kobe University Graduate School of Medicine, Kobe 650 0017, Japan
    J Biol Chem 281:40242-51. 2006
    ..These data suggest a novel mechanism by which FoxO1 regulates the insulin signaling pathway through negative regulation of TSC2 function...
  9. ncbi Transgenic rescue of insulin receptor-deficient mice
    Haruka Okamoto
    Department of Medicine, Institute of Human Nutrition, College of Physicians and Surgeons, Columbia University, New York, New York, USA
    J Clin Invest 114:214-23. 2004
    ..These data indicate, surprisingly, that insulin receptor signaling in noncanonical insulin target tissues is sufficient to maintain fuel homeostasis and prevent diabetes...
  10. ncbi Insulin/Foxo1 pathway regulates expression levels of adiponectin receptors and adiponectin sensitivity
    Atsushi Tsuchida
    Department of Internal Medicine, Graduate School of Medicine, University of Tokyo, Tokyo 113 8655, Japan
    J Biol Chem 279:30817-22. 2004
    ....
  11. ncbi Mosaic analysis of insulin receptor function
    Tadahiro Kitamura
    Department of Medicine, College of Physicians and Surgeons of Columbia University, New York, New York 10032, USA
    J Clin Invest 113:209-19. 2004
    ..These findings indicate that insulin regulates growth independently of metabolism and that the number of insulin receptors is an important determinant of the specificity of insulin action...
  12. ncbi The forkhead transcription factor Foxo1 regulates adipocyte differentiation
    Jun Nakae
    Department of Medicine, College of Physicians and Surgeons of Columbia University, New York, NY 10032, USA
    Dev Cell 4:119-29. 2003
    ..We propose that Foxo1 plays an important role in the integration of hormone-activated signaling pathways with the complex transcriptional cascade that promotes adipocyte differentiation...
  13. ncbi The forkhead transcription factor Foxo1 links insulin signaling to Pdx1 regulation of pancreatic beta cell growth
    Tadahiro Kitamura
    Naomi Berrie Diabetes Center, Department of Medicine, College of Physicians and Surgeons of Columbia University, New York, New York, USA
    J Clin Invest 110:1839-47. 2002
    ..We propose that insulin/IGFs regulate beta cell proliferation by relieving Foxo1 inhibition of Pdx1 expression in a subset of cells embedded within pancreatic ducts...
  14. ncbi Regulation of insulin action and pancreatic beta-cell function by mutated alleles of the gene encoding forkhead transcription factor Foxo1
    Jun Nakae
    Naomi Berrie Diabetes Center, Berrie Research Pavilion, 1150 St Nicholas Avenue, Department of Medicine, College of Physicians and Surgeons of Columbia University, New York, New York 10032, USA
    Nat Genet 32:245-53. 2002
    ..This has been corrected in the full-text online version of the article. The name will appear correctly in the print version...
  15. ncbi Regulation of insulin-like growth factor-dependent myoblast differentiation by Foxo forkhead transcription factors
    Marta L Hribal
    Russ Berrie Research Pavilion, Rm. 238, 1150 St. Nicholas Avenue, New York, NY 10032, USA
    J Cell Biol 162:535-41. 2003
    ..Inhibition of Foxo expression by siRNA resulted in more efficient differentiation, associated with increased myosin expression. These observations indicate that Foxo proteins are key effectors of Akt-dependent myogenesis...
  16. ncbi Inhibition of Foxo1 function is associated with improved fasting glycemia in diabetic mice
    Jennifer Altomonte
    Carl C Icahn Institute for Gene Therapy and Molecular Medicine, Mount Sinai School of Medicine, One Gustave L Levy Place, New York, NY 10029, USA
    Am J Physiol Endocrinol Metab 285:E718-28. 2003
    ..These results demonstrated that functional inhibition of Foxo1, caused by hepatic expression of its mutant, is associated with reduced hepatic gluconeogenic activity and improved fasting glycemia in diabetic mice...
  17. ncbi Defective insulin secretion in pancreatic beta cells lacking type 1 IGF receptor
    Shouhong Xuan
    Department of Genetics and Development, College of Physicians and Surgeons, Columbia University, New York, New York, USA
    J Clin Invest 110:1011-9. 2002
    ..These observations reveal a requirement of IGF1R-mediated signaling for insulin secretion...
  18. ncbi Effects of mutations in the insulin-like growth factor signaling system on embryonic pancreas development and beta-cell compensation to insulin resistance
    Yoshiaki Kido
    Department of Medicine, College of Physicians and Surgeons, Columbia University, New York, New York 10032, USA
    J Biol Chem 277:36740-7. 2002
    ..We conclude that Igf1r and Insr are required for embryonic development of the exocrine but not of the endocrine pancreas and that defects of Igf1r do not alter glucose homeostasis as long as the insulin receptor system remains intact...