Maša Skelin (Author), Jan Kopecky (Author), Jurij Dolenšek (Author), Andraž Stožer (Author)

Abstract

Background: Beta cells play a key role in the pathophysiology of diabetes since their functional adaptation is able to maintain euglycemia in the face of insulin resistance, and beta cell decompensation or dysfunction is a necessary condition for full-blown type 2 diabetes (T2D). The mechanisms behind compensation and decompensation are incompletely understood, especially for human beta cells, and even less is known about influences of chronic kidney disease (CKD) or immunosupressive therapy after transplantation on these processes and the development of posttransplant diabetes. Summary: During compensation, beta cell sensitivity to glucose becomes left-shifted, i.e., their sensitivity to stimulation increases, and this is accompanied by enhanced signals along the stimulus-secretion coupling cascade from membrane depolarization to intracellular calcium and the most distal insulin secretion dynamics. There is currently no clear evidence regarding changes in intercellular coupling during this stage of disease progression. During decompensation, intracellular stimulus-secretion coupling remains enhanced to some extent at low or basal glucose concentrations but seems to become unable to generate effective signals to stimulate insulin secretion at high or otherwise stimulatory glucose concentrations. Additionally, intercellular coupling becomes disrupted, lowering the number of cells that contribute to secretion. During progression of CKD, beta cells also seem to drift from a compensatory left-shift to failure, and immunosupressants can further impair beta cell function following kidney transplantation. Key Messages: Beta cell stimulus-secretion coupling is enhanced in compensated insulin resistance. With worsening insulin resistance, both intra- and intercellular coupling become disrupted. CKD can progressively disrupt beta cell function, but further studies are needed, especially regarding changes in intercellular coupling.

Keywords

human beta cell;functional adaptation;dysfunction;insulin resistance;

Data

Language: English
Year of publishing:
Typology: 1.03 - Short Scientific Article
Organization: UM MF - Faculty of Medicine
Publisher: S. Karger
UDC: 612
COBISS: 173873411 Link will open in a new window
ISSN: 2235-3186
Views: 9
Downloads: 0
Average score: 0 (0 votes)
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Other data

Secondary language: Slovenian
Secondary keywords: človeške beta celice;funkcionalne prilagoditve;disfunkcija;inzulinska rezistenca;
Type (COBISS): Scientific work
Pages: [v tisku] str. 1-7
Chronology: Oct. 2023
DOI: 10.1159/000534667
ID: 23435086