共 246 条
Insulin Receptor Signaling in Normal and Insulin-Resistant States
被引:1014
作者:

Boucher, Jeremie
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机构:
Brigham & Womens Hosp, Joslin Diabet Ctr, Sect Integrat Physiol & Metab, Boston, MA 02115 USA
Brigham & Womens Hosp, Dept Med, Boston, MA 02115 USA
Harvard Univ, Sch Med, Boston, MA 02115 USA Brigham & Womens Hosp, Joslin Diabet Ctr, Sect Integrat Physiol & Metab, Boston, MA 02115 USA

Kleinridders, Andre
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h-index: 0
机构:
Brigham & Womens Hosp, Joslin Diabet Ctr, Sect Integrat Physiol & Metab, Boston, MA 02115 USA
Brigham & Womens Hosp, Dept Med, Boston, MA 02115 USA
Harvard Univ, Sch Med, Boston, MA 02115 USA Brigham & Womens Hosp, Joslin Diabet Ctr, Sect Integrat Physiol & Metab, Boston, MA 02115 USA

Kahn, C. Ronald
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h-index: 0
机构:
Brigham & Womens Hosp, Joslin Diabet Ctr, Sect Integrat Physiol & Metab, Boston, MA 02115 USA
Brigham & Womens Hosp, Dept Med, Boston, MA 02115 USA
Harvard Univ, Sch Med, Boston, MA 02115 USA Brigham & Womens Hosp, Joslin Diabet Ctr, Sect Integrat Physiol & Metab, Boston, MA 02115 USA
机构:
[1] Brigham & Womens Hosp, Joslin Diabet Ctr, Sect Integrat Physiol & Metab, Boston, MA 02115 USA
[2] Brigham & Womens Hosp, Dept Med, Boston, MA 02115 USA
[3] Harvard Univ, Sch Med, Boston, MA 02115 USA
关键词:
ENDOPLASMIC-RETICULUM STRESS;
NECROSIS-FACTOR-ALPHA;
SUBSTRATE-1 TYROSINE PHOSPHORYLATION;
REGULATORY SUBUNIT P85-ALPHA;
FOXO TRANSCRIPTION FACTORS;
TYPE-2;
DIABETES-MELLITUS;
SKELETAL-MUSCLE CELLS;
HUMAN FAT-CELLS;
NF-KAPPA-B;
PROTEIN-KINASE;
D O I:
10.1101/cshperspect.a009191
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 ;
090102 ;
摘要:
In the wake of the worldwide increase in type-2 diabetes, a major focus of research is understanding the signaling pathways impacting this disease. Insulin signaling regulates glucose, lipid, and energy homeostasis, predominantly via action on liver, skeletal muscle, and adipose tissue. Precise modulation of this pathway is vital for adaption as the individual moves from the fed to the fasted state. The positive and negative modulators acting on different steps of the signaling pathway, as well as the diversity of protein isoform interaction, ensure a proper and coordinated biological response to insulin in different tissues. Whereas genetic mutations are causes of rare and severe insulin resistance, obesity can lead to insulin resistance through a variety of mechanisms. Understanding these pathways is essential for development of new drugs to treat diabetes, metabolic syndrome, and their complications.
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