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Differential regulation of embryonic and adult ? cell replication.


ABSTRACT: Diabetes results from an inadequate functional ? cell mass, either due to autoimmune destruction (Type 1 diabetes) or insulin resistance combined with ? cell failure (Type 2 diabetes). Strategies to enhance ? cell regeneration or increase cell proliferation could improve outcomes for patients with diabetes. Research conducted over the past several years has revealed that factors regulating embryonic ? cell mass expansion differ from those regulating replication of ? cells post-weaning. This article aims to compare and contrast factors known to control embryonic and postnatal ? cell replication. In addition, we explore the possibility that connective tissue growth factor (CTGF) could increase adult ? cell replication. We have already shown that CTGF is required for embryonic ? cell proliferation and is sufficient to induce replication of embryonic ? cells. Here we examine whether adult ? cell replication and expansion of ? cell mass can be enhanced by increased CTGF expression in mature ? cells.

SUBMITTER: Gunasekaran U 

PROVIDER: S-EPMC3404874 | biostudies-other | 2012 Jul

REPOSITORIES: biostudies-other

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Differential regulation of embryonic and adult β cell replication.

Gunasekaran Uma U   Hudgens Courtney W CW   Wright Brian T BT   Maulis Matthew F MF   Gannon Maureen M  

Cell cycle (Georgetown, Tex.) 20120701 13


Diabetes results from an inadequate functional β cell mass, either due to autoimmune destruction (Type 1 diabetes) or insulin resistance combined with β cell failure (Type 2 diabetes). Strategies to enhance β cell regeneration or increase cell proliferation could improve outcomes for patients with diabetes. Research conducted over the past several years has revealed that factors regulating embryonic β cell mass expansion differ from those regulating replication of β cells post-weaning. This arti  ...[more]

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