Paracrine signaling in islet function and survival.

Paracrine signaling in islet function and survival.
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DOI:
10.1007/s00109-020-01887-x
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发表时间:
2020-04
期刊:
Journal of molecular medicine (Berlin, Germany)
影响因子:
--
通讯作者:
Cox AR
Cox AR
中科院分区:
其他
文献类型:
--
作者:
Hartig SM;Cox AR

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The pancreatic islet is a dense cellular network comprised of several cell types with endocrine function vital in the control of glucose homeostasis, metabolism, and feeding behaviour. Within the islet, endocrine hormones also form an intricate paracrine network with supportive cells (endothelial, neuronal, immune) and secondary signaling molecules regulating cellular function and survival. Modulation of these signals has potential consequences for diabetes development, progression, and therapeutic intervention. Beta cell loss, reduced endogenous insulin secretion, and dysregulated glucagon secretion are hallmark features of both type 1 and 2 diabetes that impact systemic regulation of glucose, but also contribute to the function and survival of cells within the islet. Advancing research and technology has revealed new islet biology (cellular identity and transcriptomes) and identified previously unrecognized paracrine signals and mechanisms (somatostatin and ghrelin paracrine actions), while shifting prior views of intra-islet communication. This review will summarize the paracrine signals regulating islet endocrine function and survival, the disruption and dysfunction that occurs in diabetes, and potential therapeutic targets to preserve beta cell mass and function.
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