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- Title
Regulation of islet glucagon secretion: Beyond calcium.
- Authors
Hughes, Jing W.; Ustione, Alessandro; Lavagnino, Zeno; Piston, David W.
- Abstract
The islet of Langerhans plays a key role in glucose homeostasis through regulated secretion of the hormones insulin and glucagon. Islet research has focused on the insulin‐secreting β‐cells, even though aberrant glucagon secretion from α‐cells also contributes to the aetiology of diabetes. Despite its importance, the mechanisms controlling glucagon secretion remain controversial. Proper α‐cell function requires the islet milieu, where β‐ and δ‐cells drive and constrain α‐cell dynamics. The response of glucagon to glucose is similar between isolated islets and that measured in vivo, so it appears that the glucose dependence requires only islet‐intrinsic factors and not input from blood flow or the nervous system. Elevated intracellular free Ca2+ is needed for α‐cell exocytosis, but interpreting Ca2+ data is tricky since it is heterogeneous among α‐cells at all physiological glucose levels. Total Ca2+ activity in α‐cells increases slightly with glucose, so Ca2+may serve a permissive, rather than regulatory, role in glucagon secretion. On the other hand, cAMP is a more promising candidate for controlling glucagon secretion and is itself driven by paracrine signalling from β‐ and δ‐cells. Another pathway, juxtacrine signalling through the α‐cell EphA receptors, stimulated by β‐cell ephrin ligands, leads to a tonic inhibition of glucagon secretion. We discuss potential combinations of Ca2+, cAMP, paracrine and juxtacrine factors in the regulation of glucagon secretion, focusing on recent data in the literature that might unify the field towards a quantitative understanding of α‐cell function.
- Subjects
GLUCAGON regulation; CALCIUM; ISLET cell tumor; ETIOLOGY of diseases; EPHRINS
- Publication
Diabetes, Obesity & Metabolism, 2018, Vol 20, p127
- ISSN
1462-8902
- Publication type
Article
- DOI
10.1111/dom.13381