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교수진

김재범 교수

생명과학부

전공지방세포 및 에너지대사
연구실지방세포 및 에너지대사연구실
연락처02-880-4409
이메일jaebkim@snu.ac.kr

연구분야

분자생물학

세포생물학

유전학

  • Mechanism of Adipocyte Differentiation
  • Gene Expression Regulation of Lipogenesis and Insulin-dependent Genes
  • Molecular Mechanisms for Obesity and Diabetes

학력/경력

학력

1984 – 1988

  • 서울대학교 자연대학 동물학과 학사

1988 – 1990

  • 서울대학교 자연대학 동물학과 (분자생물학 전공) 석사

1991 – 1996

  • 하버드대학교 분자유전학 박사
  •  

경력

1996 – 1997

하버드대학교 Dana-Farber Cancer Institute 박사후연구원

1997 – 2000

MIT Cancer Institute 박사후연구원

2000 – Present

서울대학교 생명과학부 조교수, 부교수, 정교수

2004 – Present

한국과학기술한림원 준회원, 정회원

2005 – 2008

  • 보건복지부 국가생명윤리심의위원회 전문위원

2007 – 2008

  • Univ. of California, San Diego 초빙교수

2009 – 2011

  • 서울대학교 실험동물자원관리원장

2010 – 2014

  • 서울대학교 SPARC 부주임교수

2011 – 2012

  • 서울대학교 유전공학연구소장

2011 – Present

  • 지방조직 리모델링 창의연구단 단장, 지방세포 구조-기능 리더연구단장

2013 – 2014

  • 국가과학기술자문위원회 자문위원

2014 – 2015

  • Univ. of California, Los Angeles 초빙교수

2021 – Present

  • 한국분자세포생물학회지 (Molecules and Cells) 편집위원장 (Editor-in-Chief)

주요논문

주요논문

  • Y. S. Lee, P. Li, J. Y. Huh, I. J. Hwang, M. Lu, J. I. Kim, M. Ham, S. Talukdar, A. Chen, W. Lu, G. Bandyopadhyay, R. Schwendener, J. Olefsky, and J. B. Kim*. Inflammation is necessary for long term but not short term HFD-induced insulin resistance. Diabetes, 60:2474-2483. 2011. 10
  • I. Hwang, Y. J. Park, Y. R. Kim, Y. N. Kim, S Ka, H. Y. Lee, J. K. Seong, Y. J. Seok, and J. B. Kim*. Alteration of gut microbiota by vancomycin and bacitracin improves insulin resistance via glucagon-like peptide 1 in diet-induced obesity. FASEB J., 29:2397-411, 2015. 06. (** This paper has been highlighted in Nat. Rev. Endo. 11:254 [2015])
  • J. I. Kim, J. Y. Huh, J. H. Sohn, S. S. Choe, Y. S. Lee, C. Y. Lim, A Jo, S. B. Park, W. Han, and J. B. Kim*. Lipid-overloaded enlarged adipocytes provoke insulin resistance independent of inflammation. Mol. Cell. Biol., 35:1686-99, 2015.05 (** This paper is selected as a “Spotlight” paper. In the same issue (May 2015, Vol 35, Issue 10), Cover Figure has been selected with our data.)
  • A. Y. Kim, Y. J. Park, X. Pan, K. C. Shin, S. H. Kwak, A. F. Bassas, R. M. Sallam, K. S. Park, A. A. Alfadda, A. Xu, and J. B. Kim*. Obesity-induced DNA hypermethylation of the adiponectin gene mediates insulin resistance. Nat Commun., 6:7585, 2015. 07. (** This paper has been highlighted in Nat. Rev. Endo. 11:504 [2015])
  • H. Jang, G. Y. Lee, C. P. Selby, G. Lee, Y. G. Jeon, J. H. Lee, K. K. Y. Cheng, P. Titchenell, M. J. Birnbaum, A. Xu, A. Sancar and J. B. Kim* . SREBP1c-CRY1 signaling represses hepatic glucose production by promoting FOXO1 degradation during refeeding. Nat. Commun., 7:12180, 2016.07. (** This paper was invited from Cell Cycle journal for a Commentary Article.)
  • J. Y. Huh, J. Park, J. I. Kim, Y. J. Park, Y. K. Lee and J. B. Kim*. Deletion of CD1d in Adipocytes Aggravates Adipose Tissue Inflammation and Insulin Resistance in Obesity. Diabetes, 66:835-847, 2017.04. (** This paper was invited from Adipocyte Journal for a Commentary Review.)
  • K. C. Shin, S. S. Choe, I. J. Hwang, J. Park, J. Yul, J. I. Kim, J. Ching, J.-P. Kovalik and J. B. Kim*. Macrophage VLDLR mediates obesity-induced insulin resistance with adipose tissue inflammation. Nat Commun., 8:1087, 2017. 10.
  • I. Hwang, K. Jo, K. C. Shin, J. I. Kim, Y. Ji, Y. J. Park, J. Park, Y. G. Jeon, S. Ka, S. Suk, H. L. Noh, S. S. Choe, A. Alfadda, J. K. Kim, S. Kim and J. B. Kim*. GABA stimulated adipose-derived stem cells suppress subcutaneous adipose tissue inflammation in obesity. Proc. Natl. Acad. Sci., 116:11936-11945, 2019. 06.
  • J. Park, J. Y. Huh, J. Oh, J. I. Kim, S. M. Han, K. C. Shin, Y. G. Jeon, S. S. Choe, J. Park, and J. B. Kim*. Activation of invariant natural killer T cells stimulates adipose tissue remodeling via adipocyte death and birth in obesity. Genes & Dev., 33:1657-1672, 2019. 10.
  • J. Kong, Y. Ji, Y. G. Jeon, J. S. Han, K. H. Han, J. H. Lee, G. Lee, H. Jang, S. S. Choe, M. Baes and J. B. Kim*. Spatiotemporal contact between peroxisome and lipid droplet regulates fasting-induced lipolysis via PEX5. Nat Commun., DOI: 10.1038/s41467-019-14176-0, 2020. 01.