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线粒体磷酸酶PPTC7通过促进VPS4A在内体中的定位来促进表皮生长因子受体(EGFR)的循环利用。

Mitochondrial phosphatase PPTC7 promotes EGFR recycling by facilitating VPS4A endosomal localization.

作者信息

Baroi Rahul, Ahmad Reshi Hilal, Maddika SubbaReddy

机构信息

Laboratory of Cell Death & Cell Survival, Centre for DNA Fingerprinting and Diagnostics (CDFD), Uppal, Hyderabad 500039, India.

Graduate studies, Regional Centre for Biotechnology, Faridabad 121001, India.

出版信息

J Cell Sci. 2025 Jan 15;138(2). doi: 10.1242/jcs.263676. Epub 2025 Jan 31.

Abstract

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.

摘要

PPTC7是一种线粒体磷酸酶,对线粒体生物发生、代谢、蛋白质含量维持和运输至关重要。尽管PPTC7在线粒体中的作用已得到充分表征,但其在线粒体之外的作用尚不清楚。在这里,我们确定了PPTC7在调节表皮生长因子受体(EGFR)转运方面的非线粒体作用。PPTC7与VPS4A相互作用并使其去磷酸化,VPS4A是一种关键的内体分选转运复合体(ESCRT)和多囊泡体相关蛋白。我们发现,PPTC7介导的VPS4A丝氨酸335位点去磷酸化对于VPS4A的稳定性及其早期内体定位是必需的。PPTC7的缺失或组成型磷酸化VPS4A的存在均导致EGFR再循环缺陷,从而导致EGFR重新路由至溶酶体进行降解。此外,我们证明PPTC7-VPS4A依赖性的EGFR再循环促进AKT信号通路,从而增强细胞增殖和迁移。总体而言,我们的研究揭示了一个重要机制,即PPTC7-VPS4A复合物协调内体转换以促进EGFR再循环。

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