RhoE regulates actin cytoskeleton organization in human periodontal ligament cells under mechanical stress.

Abstract:

OBJECTIVES:RhoE and regulator of G-proteins signalling (RGS) 2 were identified as the up-regulated genes in human periodontal ligament (PDL) cells under compression. RhoE belongs to the Rho GTPase family, and RGS2, a novel family of GTPase-activating proteins, turns off the G-protein signalling. Rho family proteins have recently been known to regulate actin cytoskeleton dynamics in various cell types. In this study, we investigated the involvement of RhoE and RGS2 in the regulation of actin filament organization in the PDL cells under mechanical stress. METHODS:Human PDL cells were cultured and subjected to a static compressive force (3.0g/cm(2)) for 48h. To observe changes in the actin cytoskeleton and the expression of RhoE and RGS2 in response to mechanical stress, immunofluorescence analysis was performed. To examine the role of RhoE and RGS2 in actin filament organization, cells were transfected with antisense S-oligonucleotides (ODNs) to RhoE and RGS2. RESULTS:Compressive force caused a loss and disassembly of actin stress fibres leading to cell spreading. Immunocytochemical study revealed that RhoE and RGS2 expressions were induced by mechanical stress and localized in the perinuclear and in the cell membrane, respectively. The impaired formation of stress fibres caused by compressive forces was recovered by treatment with antisense S-ODN to RhoE to the control levels. However, addition of antisense S-ODN to RGS2 did not affect the stress fibre formation. CONCLUSIONS:These results indicate that the loss and disassembly of stress fibres due to mechanical stress are mediating RhoE signalling, without the exertion of RGS2.

journal_name

Arch Oral Biol

journal_title

Archives of oral biology

authors

de Araujo RM,Oba Y,Kuroda S,Tanaka E,Moriyama K

doi

10.1016/j.archoralbio.2013.11.010

subject

Has Abstract

pub_date

2014-02-01 00:00:00

pages

187-92

issue

2

eissn

0003-9969

issn

1879-1506

pii

S0003-9969(13)00347-6

journal_volume

59

pub_type

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