线粒体磷酸酶PPTC7通过促进VPS4A内体定位促进EGFR再循环。

IF 3.3 3区 生物学 Q3 CELL BIOLOGY
Journal of cell science Pub Date : 2025-01-15 Epub Date: 2025-01-31 DOI:10.1242/jcs.263676
Rahul Baroi, Hilal Ahmad Reshi, SubbaReddy Maddika
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引用次数: 0

摘要

PPTC7是一种线粒体磷酸酶,对线粒体的生物发生、代谢、蛋白质含量维持和运输至关重要。虽然PPTC7在线粒体中的作用已被很好地描述,但其在线粒体外的作用尚不清楚。在这里,我们确定了PPTC7在调节表皮生长因子受体(EGFR)运输中的非线粒体作用。PPTC7与关键的ESCRT和多泡体相关蛋白VPS4A相互作用并使其去磷酸化。pptc7介导的VPS4A丝氨酸335位点的去磷酸化是VPS4A稳定性及其早期内体定位所必需的。PPTC7的缺失或组成性磷酸化VPS4A的存在都会导致EGFR的再循环缺陷,从而导致EGFR重定向到溶酶体进行降解。此外,我们证明pptc7 - vps4a依赖性EGFR再循环促进AKT信号通路,从而增强细胞增殖和迁移。总的来说,我们的研究揭示了PPTC7-VPS4A复合物协调内体开关以促进EGFR再循环的重要机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Mitochondrial phosphatase PPTC7 promotes EGFR recycling by facilitating VPS4A endosomal localization.

PPTC7 is a mitochondrial phosphatase that is essential for mitochondrial biogenesis, metabolism, protein content maintenance and transport. Although the mitochondrial roles of PPTC7 are well characterized, its roles outside the mitochondria are unclear. Here we identified a non-mitochondrial role for PPTC7 in regulating epidermal growth factor receptor (EGFR) trafficking. PPTC7 interacts with and dephosphorylates VPS4A, a crucial ESCRT and multivesicular body-associated protein. We found that PPTC7-mediated dephosphorylation of VPS4A at serine 335 is required for VPS4A stability and its early endosomal localization. Either loss of PPTC7 or presence of constitutively phosphorylated VPS4A led to defective recycling of EGFR, thus leading to EGFR re-routing to lysosomes for degradation. Further, we demonstrate that PPTC7-VPS4A-dependent EGFR recycling promotes the AKT signaling pathway, thus enhancing cell proliferation and migration. Overall, our studies unveil an important mechanism where the PPTC7-VPS4A complex orchestrates an endosomal switch to promote EGFR recycling.

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来源期刊
Journal of cell science
Journal of cell science 生物-细胞生物学
CiteScore
7.30
自引率
2.50%
发文量
393
审稿时长
1.4 months
期刊介绍: Journal of Cell Science publishes cutting-edge science, encompassing all aspects of cell biology.
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