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A Ras signaling complex controls the RasC-TORC2 pathway and directed cell migration.

ABSTRACT: Ras was found to regulate Dictyostelium chemotaxis, but the mechanisms that spatially and temporally control Ras activity during chemotaxis remain largely unknown. We report the discovery of a Ras signaling complex that includes the Ras guanine exchange factor (RasGEF) Aimless, RasGEFH, protein phosphatase 2A (PP2A), and a scaffold designated Sca1. The Sca1/RasGEF/PP2A complex is recruited to the plasma membrane in a chemoattractant- and F-actin-dependent manner and is enriched at the leading edge of chemotaxing cells where it regulates F-actin dynamics and signal relay by controlling the activation of RasC and the downstream target of rapamycin complex 2 (TORC2)-Akt/protein kinase B (PKB) pathway. In addition, PKB and PKB-related PKBR1 phosphorylate Sca1 and regulate the membrane localization of the Sca1/RasGEF/PP2A complex, and thereby RasC activity, in a negative feedback fashion. Thus, our study uncovered a molecular mechanism whereby RasC activity and the spatiotemporal activation of TORC2 are tightly controlled at the leading edge of chemotaxing cells.

SUBMITTER: Charest PG

PROVIDER: S-EPMC2893887 | biostudies-literature | 2010 May

REPOSITORIES: biostudies-literature

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A Ras signaling complex controls the RasC-TORC2 pathway and directed cell migration.

Charest Pascale G PG Shen Zhouxin Z Lakoduk Ashley A Sasaki Atsuo T AT Briggs Steven P SP Firtel Richard A RA

Developmental cell 20100501 5

Ras was found to regulate Dictyostelium chemotaxis, but the mechanisms that spatially and temporally control Ras activity during chemotaxis remain largely unknown. We report the discovery of a Ras signaling complex that includes the Ras guanine exchange factor (RasGEF) Aimless, RasGEFH, protein phosphatase 2A (PP2A), and a scaffold designated Sca1. The Sca1/RasGEF/PP2A complex is recruited to the plasma membrane in a chemoattractant- and F-actin-dependent manner and is enriched at the leading ed ...[more]

PMID: 20493808

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Project description:The enhanced migratory ability of endometrial stromal cells (ESCs) is a key factor in the formation of functional endometrium?like tissues outside the uterine cavity during endometriosis (EMS). Although accumulating evidence has suggested the importance of microRNAs (miRNAs) in the pathogenesis of EMS, the role of particular miRNAs in the invasiveness of ESCs remain poorly understood. In the present study, the function of miRNAs in the invasiveness of ESCs, along with the associated underlying mechanism involved, were investigated. Initially, the expression patterns of miRNAs in the ectopic and eutopic endometrium isolated from patients with EMS were analyzed using microarray. MicroRNA?202?5p (miR?202) was selected for further study due to its previously reported suppressive effects on the invasion in various types of cancers. The expression of miR?202 and K?Ras in eutopic and ectopic endometrioma tissues were detected using reverse transcription?quantitative PCR, immunohistochemistry and western blotting. The migration and invasion ability of ESCs was determined using wound healing and Transwell invasion assays, respectively. Compared with that from healthy individuals, miR?202 expression was demonstrated to be lower in the eutopic endometrium from patients with EMS, which was even lower in ectopic endometrium. Functional experiments in primary ESCs revealed that enhanced miR?202 expression suppressed the cell invasion and migration abilities, which was also accompanied with increased E?cadherin and reduced N?cadherin expression in ESCs, suggesting its potentially suppressive role in epithelial?mesenchymal transition. K?Ras is a well?known regulator of the ERK signaling pathway that was shown to be directly targeted and negatively regulated by miR?202. In addition, K?Ras expression was found to be upregulated in the ectopic endometrium, where it correlated negatively with that of miR?202. Knocking down K?Ras expression mimicked the anti?invasive effects of miR?202 overexpression on ESCs, whilst K?Ras overexpression attenuated the inhibitory role of miR?202 overexpression in ESC invasion. The K?Ras/Raf1/MEK/ERK signaling pathway was also blocked by miR?202 overexpression. These findings suggested that miR?202 inhibited ESC migration and invasion by inhibiting the K?Ras/Raf1/MEK/ERK signaling pathway, rendering miR?202 a candidate for being a therapeutic target for EMS.

Dataset Information

A Ras signaling complex controls the RasC-TORC2 pathway and directed cell migration.

Publications

A Ras signaling complex controls the RasC-TORC2 pathway and directed cell migration.

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