δ-Cells: The Neighborhood Watch in the Islet Community
Somatostatin-secreting δ-cells have aroused great attention due to their powerful roles in coordination of islet insulin and glucagon secretion and maintenance of glucose homeostasis. δ-cells exhibit neuron-like morphology with projections which enable pan-islet somatostatin paracrine regulation des...
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doaj-2e37393904bb43d596b8c16103672e952021-01-22T00:00:57ZengMDPI AGBiology2079-77372021-01-0110747410.3390/biology10020074δ-Cells: The Neighborhood Watch in the Islet CommunityRui Gao0Tao Yang1Quan Zhang2Oxford Centre for Diabetes, Endocrinology and Metabolism, Radcliffe Department of Medicine, University of Oxford, Oxford OX3 7LE, UKDepartment of Endocrinology and Metabolism, The First Affiliated Hospital of Nanjing Medical University, Nanjing 210029, ChinaOxford Centre for Diabetes, Endocrinology and Metabolism, Radcliffe Department of Medicine, University of Oxford, Oxford OX3 7LE, UKSomatostatin-secreting δ-cells have aroused great attention due to their powerful roles in coordination of islet insulin and glucagon secretion and maintenance of glucose homeostasis. δ-cells exhibit neuron-like morphology with projections which enable pan-islet somatostatin paracrine regulation despite their scarcity in the islets. The expression of a range of hormone and neurotransmitter receptors allows δ-cells to integrate paracrine, endocrine, neural and nutritional inputs, and provide rapid and precise feedback modulations on glucagon and insulin secretion from α- and β-cells, respectively. Interestingly, the paracrine tone of δ-cells can be effectively modified in response to factors released by neighboring cells in this interactive communication, such as insulin, urocortin 3 and γ-aminobutyric acid from β-cells, glucagon, glutamate and glucagon-like peptide-1 from α-cells. In the setting of diabetes, defects in δ-cell function lead to suboptimal insulin and glucagon outputs and lift the glycemic set-point. The interaction of δ-cells and non-δ-cells also becomes defective in diabetes, with reduces paracrine feedback to β-cells to exacerbate hyperglycemia or enhanced inhibition of α-cells, disabling counter-regulation, to cause hypoglycemia. Thus, it is possible to restore/optimize islet function in diabetes targeting somatostatin signaling, which could open novel avenues for the development of effective diabetic treatments.https://www.mdpi.com/2079-7737/10/2/74pancreatic δ-cellssomatostatinparacrine regulationintra-islet coordinationdiabetes |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Rui Gao Tao Yang Quan Zhang |
spellingShingle |
Rui Gao Tao Yang Quan Zhang δ-Cells: The Neighborhood Watch in the Islet Community Biology pancreatic δ-cells somatostatin paracrine regulation intra-islet coordination diabetes |
author_facet |
Rui Gao Tao Yang Quan Zhang |
author_sort |
Rui Gao |
title |
δ-Cells: The Neighborhood Watch in the Islet Community |
title_short |
δ-Cells: The Neighborhood Watch in the Islet Community |
title_full |
δ-Cells: The Neighborhood Watch in the Islet Community |
title_fullStr |
δ-Cells: The Neighborhood Watch in the Islet Community |
title_full_unstemmed |
δ-Cells: The Neighborhood Watch in the Islet Community |
title_sort |
δ-cells: the neighborhood watch in the islet community |
publisher |
MDPI AG |
series |
Biology |
issn |
2079-7737 |
publishDate |
2021-01-01 |
description |
Somatostatin-secreting δ-cells have aroused great attention due to their powerful roles in coordination of islet insulin and glucagon secretion and maintenance of glucose homeostasis. δ-cells exhibit neuron-like morphology with projections which enable pan-islet somatostatin paracrine regulation despite their scarcity in the islets. The expression of a range of hormone and neurotransmitter receptors allows δ-cells to integrate paracrine, endocrine, neural and nutritional inputs, and provide rapid and precise feedback modulations on glucagon and insulin secretion from α- and β-cells, respectively. Interestingly, the paracrine tone of δ-cells can be effectively modified in response to factors released by neighboring cells in this interactive communication, such as insulin, urocortin 3 and γ-aminobutyric acid from β-cells, glucagon, glutamate and glucagon-like peptide-1 from α-cells. In the setting of diabetes, defects in δ-cell function lead to suboptimal insulin and glucagon outputs and lift the glycemic set-point. The interaction of δ-cells and non-δ-cells also becomes defective in diabetes, with reduces paracrine feedback to β-cells to exacerbate hyperglycemia or enhanced inhibition of α-cells, disabling counter-regulation, to cause hypoglycemia. Thus, it is possible to restore/optimize islet function in diabetes targeting somatostatin signaling, which could open novel avenues for the development of effective diabetic treatments. |
topic |
pancreatic δ-cells somatostatin paracrine regulation intra-islet coordination diabetes |
url |
https://www.mdpi.com/2079-7737/10/2/74 |
work_keys_str_mv |
AT ruigao dcellstheneighborhoodwatchintheisletcommunity AT taoyang dcellstheneighborhoodwatchintheisletcommunity AT quanzhang dcellstheneighborhoodwatchintheisletcommunity |
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