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Mol. Cells 2010; 30(6): 563-567

Published online November 18, 2010

https://doi.org/10.1007/s10059-010-0153-5

© The Korean Society for Molecular and Cellular Biology

Chemoattractant-Mediated Rap1 Activation Requires GPCR/G Proteins

Injun Cha, Sung H. Lee1, and Taeck J. Jeon*

Department of Biology, College of Natural Sciences, Chosun University, Gwangju 501-759, Korea, 1Department of Cellular and Molecular Medicine, School of medicine, Chosun University, Gwangju 501-759, Korea

Correspondence to : *Correspondence: tjeon@chosun.ac.kr

Received: August 10, 2010; Revised: September 8, 2010; Accepted: September 10, 2010

Abstract

Rap1 is rapidly activated upon chemoattractant stimula-tion and plays an important role in cell adhesion and cytoskeletal reorganization during chemotaxis. Here, we de-monstrate that G-protein coupled receptors and G-proteins are essential for chemoattractant-mediated Rap1 activation in Dictyostelium. The rapid Rap1 activation upon cAMP chemoattractant stimulation was absent in cells lacking chemoattractant cAMP receptors cAR1/cAR3 or a subunit of the heterotrimeric G-protein complex Gα2. Loss of guanylyl cyclases GCA/SGC or a cGMP-binding protein GbpC exhibited no effect on Rap1 activation kinetics. These results suggest that Rap1, a key regulator for the regulation of cytoskeletal reorganization during cell move-ment, is activated through the G-protein coupled receptors cAR1/cAR3 and Gα2 proteins in a way independent of the cGMP signaling pathway.

Keywords chemotaxis, Dictyostelium, GPCR, Rap1, signal transduction

Article

Research Article

Mol. Cells 2010; 30(6): 563-567

Published online December 31, 2010 https://doi.org/10.1007/s10059-010-0153-5

Copyright © The Korean Society for Molecular and Cellular Biology.

Chemoattractant-Mediated Rap1 Activation Requires GPCR/G Proteins

Injun Cha, Sung H. Lee1, and Taeck J. Jeon*

Department of Biology, College of Natural Sciences, Chosun University, Gwangju 501-759, Korea, 1Department of Cellular and Molecular Medicine, School of medicine, Chosun University, Gwangju 501-759, Korea

Correspondence to:*Correspondence: tjeon@chosun.ac.kr

Received: August 10, 2010; Revised: September 8, 2010; Accepted: September 10, 2010

Abstract

Rap1 is rapidly activated upon chemoattractant stimula-tion and plays an important role in cell adhesion and cytoskeletal reorganization during chemotaxis. Here, we de-monstrate that G-protein coupled receptors and G-proteins are essential for chemoattractant-mediated Rap1 activation in Dictyostelium. The rapid Rap1 activation upon cAMP chemoattractant stimulation was absent in cells lacking chemoattractant cAMP receptors cAR1/cAR3 or a subunit of the heterotrimeric G-protein complex Gα2. Loss of guanylyl cyclases GCA/SGC or a cGMP-binding protein GbpC exhibited no effect on Rap1 activation kinetics. These results suggest that Rap1, a key regulator for the regulation of cytoskeletal reorganization during cell move-ment, is activated through the G-protein coupled receptors cAR1/cAR3 and Gα2 proteins in a way independent of the cGMP signaling pathway.

Keywords: chemotaxis, Dictyostelium, GPCR, Rap1, signal transduction

Mol. Cells
Sep 30, 2023 Vol.46 No.9, pp. 527~572
COVER PICTURE
Chronic obstructive pulmonary disease (COPD) is marked by airspace enlargement (emphysema) and small airway fibrosis, leading to airflow obstruction and eventual respiratory failure. Shown is a microphotograph of hematoxylin and eosin (H&E)-stained histological sections of the enlarged alveoli as an indicator of emphysema. Piao et al. (pp. 558-572) demonstrate that recombinant human hyaluronan and proteoglycan link protein 1 (rhHAPLN1) significantly reduces the extended airspaces of the emphysematous alveoli by increasing the levels of TGF-β receptor I and SIRT1/6, as a previously unrecognized mechanism in human alveolar epithelial cells, and consequently mitigates COPD.

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