Type 2 diabetes disrupts circadian orchestration of lipid metabolism and membrane fluidity in human pancreatic islets
PLoS Biology, ISSN: 1545-7885, Vol: 20, Issue: 8, Page: e3001725
2022
- 11Citations
- 23Captures
- 2Mentions
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- Citations11
- Citation Indexes11
- 11
- Captures23
- Readers23
- 22
- Mentions2
- News Mentions2
- News2
Most Recent News
Diabetes: When circadian lipid rhythms go wrong
Like all living beings, human physiological processes are influenced by circadian rhythms. The disruption of our internal clocks due to an increasingly unbalanced lifestyle is directly linked to the explosion in cases of type 2 diabetes. By what mechanism? A team is lifting part of the veil: this disturbance disrupts the metabolism of lipids in the cells that secrete glucose-regulating hormones. S
Article Description
ARUec:ePnlteeavsiedceonncfiermstuhgagtaelslhtseatdhiantgcleirvcealsdaiarenrecplorceskesnetendscuorreretcetmly:poral orchestration of lipid homeostasis and play a role in pathophysiology of metabolic diseases in humans, including type 2 diabetes (T2D). Nevertheless, circadian regulation of lipid metabolism in human pancreatic islets has not been explored. Employing lipidomic analyses, we conducted temporal profiling in human pancreatic islets derived from 10 nondiabetic (ND) and 6 T2D donors. Among 329 detected lipid species across 8 major lipid classes, 5% exhibited circadian rhythmicity in ND human islets synchronized in vitro. Two-time point-based lipidomic analyses in T2D human islets revealed global and temporal alterations in phospho- and sphingolipids. Key enzymes regulating turnover of sphingolipids were rhythmically expressed in ND islets and exhibited altered levels in ND islets bearing disrupted clocks and in T2D islets. Strikingly, cellular membrane fluidity, measured by a Nile Red derivative NR12S, was reduced in plasma membrane of T2D diabetic human islets, in ND donors' islets with disrupted circadian clockwork, or treated with sphingolipid pathway modulators. Moreover, inhibiting the glycosphingolipid biosynthesis led to strong reduction of insulin secretion triggered by glucose or KCl, whereas inhibiting earlier steps of de novo ceramide synthesis resulted in milder inhibitory effect on insulin secretion by ND islets. Our data suggest that circadian clocks operative in human pancreatic islets are required for temporal orchestration of lipid homeostasis, and that perturbation of temporal regulation of the islet lipid metabolism upon T2D leads to altered insulin secretion and membrane fluidity. These phenotypes were recapitulated in ND islets bearing disrupted clocks.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85135500829&origin=inward; http://dx.doi.org/10.1371/journal.pbio.3001725; http://www.ncbi.nlm.nih.gov/pubmed/35921354; https://dx.plos.org/10.1371/journal.pbio.3001725; https://dx.doi.org/10.1371/journal.pbio.3001725; https://journals.plos.org/plosbiology/article?id=10.1371/journal.pbio.3001725
Public Library of Science (PLoS)
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