Aging and regional differences in fat cell progenitors - A mini-review

Anna Sepe, Tamara Tchkonia, Thomas Thomou, Mauro Zamboni, James L. Kirkland

Research output: Contribution to journalReview articlepeer-review

130 Scopus citations


Fat mass and fat tissue distribution change dramatically throughout life. In old age, fat becomes dysfunctional and is redistributed from subcutaneous to intra-abdominal visceral depots as well as other ectopic sites, including bone marrow, muscle and the liver. These changes are associated with increased risk of metabolic syndrome. Fat tissue is a nutrient storage, endocrine and immune organ that undergoes renewal throughout the lifespan. Preadipocytes, which account for 15-50% of cells in fat tissue, give rise to new fat cells. With aging, declines in preadipocyte proliferation and differentiation likely contribute to increased systemic exposure to lipotoxic free fatty acids. Age-related fat tissue inflammation is related to changes that occur in preadipocytes and macrophages in a fat depot-dependent manner. Fat tissue inflammation frequently leads to further reduction in adipogenesis with aging, more lipotoxicity and activation of cellular stress pathways that, in turn, exacerbate inflammatory responses of preadipocytes and immune cells, establishing self-perpetuating cycles that lead to systemic dysfunction. In this review, we will consider how inherent, age-related, depot-dependent alterations in preadipocyte function contribute to age-related fat tissue redistribution and metabolic dysfunction.

Original languageEnglish (US)
Pages (from-to)66-75
Number of pages10
Issue number1
StatePublished - Dec 2010


  • Fat depot
  • Fat redistribution
  • Inflammation
  • Preadipocytes

ASJC Scopus subject areas

  • Aging
  • Geriatrics and Gerontology


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