Humanin: Functional Interfaces with IGF-I

被引:32
作者
Xiao, J. [1 ]
Kim, S. -J. [1 ]
Cohen, P. [1 ]
Yen, K. [1 ]
机构
[1] Univ Southern Calif, Leonard Davis Sch Gerontol, Los Angeles, CA 90089 USA
关键词
Humanin; IGF-I; Growth hormone; Mitochondria; Neuroprotection; Peptide; GROWTH-FACTOR-I; AMYLOID PRECURSOR PROTEIN; RESCUE FACTOR HUMANIN; NEURONAL CELL-DEATH; NEUROPROTECTIVE FACTOR; BINDING PROTEIN-3; MYOCARDIAL-ISCHEMIA; REPERFUSION INJURY; PEPTIDE HUMANIN; INSULIN;
D O I
10.1016/j.ghir.2016.03.005
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Humanin is the first newly discovered peptide encoded in the mitochondrial genome in over three decades. It is the first member of a novel class of mitochondrial derived peptides. This small, 24 amino acid peptide was initially discovered to have neuroprotective effects and subsequent experiments have shown that it is beneficial in a diverse number of disease models including stroke, cardiovascular disease, and cancer. Over a decade ago, our lab found that humanin bound IGFBP-3 and more recent studies have found it to decrease circulating IGF-I levels. In turn, IGF-I also seems to regulate humanin levels and in this review, we cover the known interaction between humanin and IGF-I. Although the exact mechanism for how humanin and IGF-I regulate each other still needs to be elucidated, it is clear that humanin is a new player in IGF-I signaling. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:21 / 27
页数:7
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