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Int J Mol Sci ; 24(14)2023 Jul 17.
Artigo em Inglês | MEDLINE | ID: mdl-37511311

RESUMO

Ninjurin 1 (NINJ1) is a double-transmembrane cell-surface protein that might mediate plasma membrane rupture (PMR) and the diffusion of inflammatory factors. PMR is a characteristic of acinar cell injury in severe acute pancreatitis (SAP). However, the involvement of NINJ1 in mediating the PMR of acinar cells in SAP is currently unclear. Our study has shown that NINJ1 is expressed in acinar cells, and the expression is significantly upregulated in sodium-taurocholate-induced SAP. The knockout of NINJ1 delays PMR in acinar cells and alleviates SAP. Moreover, we observed that NINJ1 expression is mediated by Ca2+ concentration in acinar cells. Importantly, we found that Ca2+ overload drives mitochondrial stress to upregulate the P53/NINJ1 pathway, inducing PMR in acinar cells, and amlodipine, a Ca2+ channel inhibitor, can reduce the occurrence of PMR by decreasing the concentration of Ca2+. Our results demonstrate the mechanism by which NINJ1 induces PMR in SAP acinar cells and provide a potential new target for treatment of SAP.


Assuntos
Células Acinares , Cálcio , Membrana Celular , Pancreatite , Proteína Supressora de Tumor p53 , Humanos , Células Acinares/metabolismo , Células Acinares/patologia , Doença Aguda , Cálcio/metabolismo , Cálcio da Dieta/metabolismo , Moléculas de Adesão Celular Neuronais/metabolismo , Membrana Celular/metabolismo , Membrana Celular/patologia , Fatores de Crescimento Neural/metabolismo , Pancreatite/metabolismo , Pancreatite/patologia , Pancreatite/fisiopatologia , Proteína Supressora de Tumor p53/genética , Proteína Supressora de Tumor p53/metabolismo
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