Very slow turnover of β-cells in aged adult mice

被引:401
作者
Teta, M
Long, SY
Wartschow, LM
Rankin, MM
Kushner, JA
机构
[1] Univ Penn, Childrens Hosp Philadelphia, Div Endocrinol, Sch Med, Philadelphia, PA 19104 USA
[2] Harvard Univ, Sch Med, Childrens Hosp, Div Endocrinol, Boston, MA USA
关键词
D O I
10.2337/diabetes.54.9.2557
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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 similar to 1,400 adult beta-cells were found to undergo replication per day. We conclude that adult beta-cells are very long lived.
引用
收藏
页码:2557 / 2567
页数:11
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