Src-mediated Tyr353 phosphorylation of IP3R1 promotes its stability and causes apoptosis in palmitic acid-treated hepatocytes
Src 介导的 IP3R1 Tyr353 磷酸化促进其稳定性并导致棕榈酸处理的肝细胞凋亡
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作者:Ting Yu, Enze Zheng, Yanping Li, Yuqi Li, Jun Xia, Qiuying Ding, Zhengping Hou, Xiong Z Ruan, Lei Zhao, Yaxi Chen
| 期刊: | Experimental Cell Research | 影响因子: | 3.300 |
| 时间: | 2021 | 起止号: | 2021 Feb 15;399(2):112438. |
| doi: | 10.1016/j.yexcr.2020.112438 | 研究方向: | 信号转导、细胞生物学、表观遗传 |
| 细胞类型: | 其它细胞 | 信号通路: | Apoptosis |
Conclusion
PA promotes the Tyr353 phosphorylation of IP3R1 by activating the src pathway and increasing the protein stability of IP3R1, which consequently results in mitochondrial Ca2+ overload and mitochondrial dysfunction in hepatic cells. Our results also suggested that inhibition of the src/IP3R1 pathway, such as by SU6656, may be a novel potential therapeutic approach for the treatment of NAFLD.
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