β-Cell mass dynamics and islet cell plasticity in human type 2 diabetes
Endocrinology, ISSN: 0013-7227, Vol: 151, Issue: 4, Page: 1462-1472
2010
- 130Citations
- 98Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
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Metrics Details
- Citations130
- Citation Indexes130
- 130
- CrossRef64
- Captures98
- Readers98
- 98
Article Description
Studies of long-standing type 2 diabetes (T2D) report a deficit in β-cell mass due to increased apoptosis, whereas neogenesis and replication are unaffected. It is unclear whether these changes are a cause or a consequence of T2D. Moreover, whereas islet morphogenetic plasticity has been demonstrated in vitro, the in situ plasticity of islets, as well as the effect of T2D on endocrine differentiation, is unknown. We compared β-cell volume, neogenesis, replication, and apoptosis in pancreata from lean and obese (body mass index ≥ 27 kg/m) diabetic (5 ± 2 yr since diagnosis) and nondiabetic cadaveric donors. We also subjected isolated islets from diabetic (3 ± 1 yr since diagnosis) and nondiabetic donors to an established in vitro model of islet plasticity. Differences in β-cell volume between diabetic and nondiabetic donors were consistently less pronounced than those reported in long-standing T2D. A compensatory increase in β-cell neogenesis appeared to mediate this effect. Studies of induced plasticity indicated that islets from diabetic donors were capable of epithelial dedifferentiation but did not demonstrate regenerative potential, as was seen in islets from nondiabetic donors. This deficiency was associated with the overexpression of Notch signaling molecules and a decreased neurogenin-3 cell frequency. One interpretation of these results would be that decreased β-cell volume is a consequence, not a cause, of T2D, mediated by increased apoptosis and attenuated β-cell (re)generation. However, other explanations are also possible. It remains to be seen whether the morphogenetic plasticity of human islets, deficient in vitro in islets from diabetic donors, is a component of normal β-cell mass dynamics. Copyright © 2010 by The Endocrine Society.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=77950290798&origin=inward; http://dx.doi.org/10.1210/en.2009-1277; http://www.ncbi.nlm.nih.gov/pubmed/20176718; https://academic.oup.com/endo/article/151/4/1462/2456643; https://dx.doi.org/10.1210/en.2009-1277; https://academic.oup.com/endo/article-abstract/151/4/1462/2456643?redirectedFrom=fulltext
The Endocrine Society
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