Very slow turnover of beta-cells in aged adult mice

Diabetes. 2005 Sep;54(9):2557-67. doi: 10.2337/diabetes.54.9.2557.

Abstract

Although many signaling pathways have been shown to promote beta-cell growth, surprisingly little is known about the normal life cycle of preexisting beta-cells or the signaling pathways required for beta-cell survival. Adult beta-cells have been speculated to have a finite life span, with ongoing adult beta-cell replication throughout life to replace lost cells. However, little solid evidence supports this idea. To more accurately measure adult beta-cell turnover, we performed continuous long-term labeling of proliferating cells with the DNA precursor analog 5-bromo-2-deoxyuridine (BrdU) in 1-year-old mice. We show that beta-cells of aged adult mice have extremely low rates of replication, with minimal evidence of turnover. Although some pancreatic components acquired BrdU label in a linear fashion, only 1 in approximately 1,400 adult beta-cells were found to undergo replication per day. We conclude that adult beta-cells are very long lived.

MeSH terms

  • Aging / physiology*
  • Animals
  • Bromouracil / analogs & derivatives
  • Cell Death
  • Cell Proliferation / drug effects
  • Female
  • Glucagon / metabolism
  • Islets of Langerhans / cytology*
  • Islets of Langerhans / physiology*
  • Male
  • Mice
  • Pancreatic Polypeptide / metabolism
  • Somatostatin / metabolism
  • Streptozocin / pharmacology
  • Uridine / analogs & derivatives

Substances

  • Bromouracil
  • Somatostatin
  • Pancreatic Polypeptide
  • Streptozocin
  • Glucagon
  • 5-bromouridine
  • Uridine