ER Stress-Induced β-Cell Apoptosis is Linked to Novel Select Lipid Signaling at the Transcriptional Level: Implications in T1D Developmen <i>t</i>
Type 1 diabetes (T1D) is a consequence of β-cell death. ER stress precedes T1D onset and prolonged ER stress in β-cells can lead to β-cell apoptosis. We reported that lipid signaling generated by the Ca <sup>2+</sup> -independent phospholipase A <sub>2</sub> β (iPLA <sub>2</sub> β), encoded by <i>Pla2g6</i> , participates in ER stress-mediated β-cell apoptosis. β-Cell membranes are enriched in arachidonic acid containing glycerophospholipids and the iPLA <sub>2</sub> β catalyzes the hydrolysis of arachidonic acid in ER stressed β-cells. Metabolism of arachidonic acid leads to the generation of various proinflammatory lipids, raising the possibility that they contribute to ER stress and β-cell death leading to T1D. However, molecular mechanisms by which such β-cell-iPLA <sub>2</sub> β-derived lipid (iDL) signaling contributes to β-cell apoptosis are not understood. It is well known that ER stress-mediated β-cell apoptosis is associated with induction of transcription factors, NFκB and STAT1. We report here that both induce <i>Pla2g6</i> and, unexpectedly, we find that iPLA <sub>2</sub> β, which lacks DNA-binding motifs, associates with <i>NFkB</i> , <i>Stat1</i> , and <i>Pla2g6</i> promoter regions. Consistently, p65-NFκB and pSTAT1 induction is reduced with select inhibition or knockdown of iPLA <sub>2</sub> β. Surprisingly, iPLA <sub>2</sub> β expression is also reduced by select inhibition of iPLA <sub>2</sub> β, raising the possibility of feedback regulation by iDLs. In support, we find that select iDLs, recognized to be proinflammatory, enhance association of iPLA <sub>2</sub> β with <i>Pla2g6</i> , <i>Nfkb</i> , and <i>Stat1</i> promoter regions leading to induction of all three gene products and β-cell apoptosis. Our findings reveal previously unrecognized transcriptional regulation by iDL signaling and, iPLA <sub>2</sub> β itself, that leads to gene products that promote β-cell apoptosis. Analogous findings in human islets validate this mechanism raising the possibility that targeting select lipid signaling can reduce ER stress in β-cells and ameliorate T1D development.
Authors
- Charles E. Chalfant (ORCID: https://orcid.org/0000-0002-5844-5235)
- Anil K. Challa (ORCID: https://orcid.org/0000-0002-3633-3304)
- Susan E. Nozell (ORCID: https://orcid.org/0000-0003-2960-4484)
- Xiaoyong Lei
- Sasanka Ramanadham
- Daniel Stephenson (ORCID: https://orcid.org/0000-0002-5698-3400)
- Chad S. Hunter
- Adam R. Wende (ORCID: https://orcid.org/0000-0002-5536-4675)
- Ying Gai-Tusing
- Andrew Nafzinger
- Tomader Ali
Institutions
- Pacific Northwest National Laboratory (US)
- Baze University (NG)
- University of Alabama at Birmingham (US)
- University of Kansas Medical Center (US)
- VA Central California Health Care System (US)
- University of Virginia (US)
Publication Details
- Journal
- bioRxiv (Cold Spring Harbor Laboratory)
- Published
- 2026-03-04
- DOI
- https://doi.org/10.64898/2026.03.02.708596
- Primary Topic
- Pancreatic function and diabetes
- Type
- article
- Field-Weighted Citation Impact
- 0.00