Growth signaling and longevity in mouse models

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19
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20

초록

Reduction of insulin/insulin-like growth factor 1 (IGF1) signaling (IIS) extends the lifespan of various species. So far, several longevity mouse models have been developed containing mutations related to growth signaling deficiency by targeting growth hormone (GH), IGF1, IGF1 receptor, insulin receptor, and insulin receptor substrate. In addition, p70 ribosomal protein S6 kinase 1 (S6K1) knockout leads to lifespan extension. S6K1 encodes an important kinase in the regulation of cell growth. S6K1 is regulated by mechanistic target of rapamycin (mTOR) complex 1. The v-myc myelocytomatosis viral oncogene homolog (MYC)-deficient mice also exhibits a longevity phenotype. The gene expression profiles of these mice models have been measured to identify their longevity mechanisms. Here, we summarize our knowledge of long-lived mouse models related to growth and discuss phenotypic characteristics, including organ-specific gene expression patterns.

키워드

Gene expressionGrowth signalingLongevityMouse modelLIFE-SPAN EXTENSIONLONG-LIVED SNELLGENE-EXPRESSION PROFILEWHITE ADIPOSE-TISSUEAMES DWARF MICEOXIDATIVE STRESSIGF-IDIETARY RESTRICTIONINSULIN-RESISTANCESEXUAL-DIMORPHISM
제목
Growth signaling and longevity in mouse models
저자
Kim, Seung-SooLee, Cheol-Koo
DOI
10.5483/BMBRep.2019.52.1.299
발행일
2019-01-31
유형
Review
저널명
BMB Reports
52
1
페이지
70 ~ 85