Growth hormone action predicts age-related white adipose tissue dysfunction and senescent cell burden in mice
Abbreviated Journal Title
adipose tissue; aging; cellular senescence; growth hormone; LIFE-SPAN EXTENSION; BODY-COMPOSITION; PRECURSOR CELLS; GENE-EXPRESSION; AMES DWARF; STEM-CELLS; ADIPOCYTE DIFFERENTIATION; ADIPOGENIC FACTORS; TRANSGENIC MICE; ANATOMIC SITE; Cell Biology
The aging process is associated with the development of several chronic diseases. White adipose tissue (WAT) may play a central role in age-related disease onset and progression due to declines in adipogenesis with advancing age. Recent reports indicate that the accumulation of senescent progenitor cells may be involved in age-related WAT dysfunction. Growth hormone (GH) action has profound effects on adiposity and metabolism and is known to influence lifespan. In the present study we tested the hypothesis that GH activity would predict age-related WAT dysfunction and accumulation of senescent cells. We found that long-lived GH-deficient and -resistant mice have reduced age-related lipid redistribution. Primary preadipocytes from GH-resistant mice also were found to have greater differentiation capacity at 20 months of age when compared to controls. GH activity was also found to be positively associated with senescent cell accumulation in WAT. Our results demonstrate an association between GH activity, age-related WAT dysfunction, and WAT senescent cell accumulation in mice. Further studies are needed to determine if GH is directly inducing cellular senescence in WAT or if GH actions on other target organs or alternative downstream alterations in insulin-like growth factor-1, insulin or glucose levels are responsible.
"Growth hormone action predicts age-related white adipose tissue dysfunction and senescent cell burden in mice" (2014). Faculty Bibliography 2010s. 6135.