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.

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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
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article
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article

ER Stress-Induced β-Cell Apoptosis is Linked to Novel Select Lipid Signaling at the Transcriptional Level: Implications in T1D Developmen t

Charles E. Chalfant, Anil K. Challa, Susan E. Nozell, Xiaoyong Lei et al.
bioRxiv (Cold Spring Harbor Laboratory)
Pancreatic function and diabetes
article

ER Stress-Induced β-Cell Apoptosis is Linked to Novel Select Lipid Signaling at the Transcriptional Level: Implications in T1D Developmen t

Charles E. Chalfant, Anil K. Challa, Susan E. Nozell, Xiaoyong Lei, Sasanka Ramanadham, Daniel Stephenson, Chad S. Hunter, Adam R. Wende, Ying Gai-Tusing, Andrew Nafzinger, Tomader Ali
article en

Abstract

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.

bioRxiv (Cold Spring Harbor Laboratory)
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)
Good health and well-being
Openalex Percentile: Top 32%
Pancreatic function and diabetes
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