SNAP23 decreases insulin secretion by competitively inhibiting the interaction between SNAP25 and STX1A.

Jun Chen, Ziyan Wang, Tuanlao Wang, Jidong Cheng, Ruijuan Zhuang, Wei Wang

Bioscience reports 2023 May 31

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SNAP25 is a core protein of the SNARE complex, which mediates stimulus-dependent secretion of insulin from the pancreatic β cells. SNAP23 is a SNAP25 homolog, however, the functional role of SNAP23 in the exocytic secretion of insulin is not known. Therefore, in the present study, we investigated the functional role of SNAP23 in the insulin secretory pathway. Our results demonstrated that over-expression of SNAP23 inhibited the secretion of insulin from the INS-1 cells. Conversely, SNAP23 depletion increased insulin secretion. Mechanistically, overexpression of SNAP23 decreased SNARE complex formation by blocking the binding of SNAP25 to STX1A. The full-length SNAP23 protein with the N-terminal and C-terminal SNARE binding domains was required for competition. Moreover, SNAP23 serine 95 phosphorylation plays a crucial function in insulin secretion by enhancing the interaction between SNAP23 and STX1A. The present study presents a new pathway regulating insulin secretion. Therefore, SNAP23 may be a potential therapeutic target for diabetes mellitus. © 2023 The Author(s).

Citation

Jun Chen, Ziyan Wang, Tuanlao Wang, Jidong Cheng, Ruijuan Zhuang, Wei Wang. SNAP23 decreases insulin secretion by competitively inhibiting the interaction between SNAP25 and STX1A. Bioscience reports. 2023 May 31;43(5)