RhoA expression during recovery from skeletal muscle disuse
Open Access
- 1 April 2004
- journal article
- Published by American Physiological Society in Journal of Applied Physiology
- Vol. 96 (4) , 1341-1348
- https://doi.org/10.1152/japplphysiol.01015.2003
Abstract
Functional overload and anabolic steroid administration induce signaling pathways that regulate skeletal muscle RhoA expression. The purpose of this study was to determine RhoA and associated protein expression at the onset of disuse and after a brief period of reloading. Male Sprague-Dawley rats were randomly assigned to cage control (Con), 3 days of hindlimb suspension (Sus), or 3 days of hindlimb suspension with 12 h of reloading (12-h Reload). The reloading stimuli consisted of 12 h of resumed normal locomotion after 3 days of hindlimb suspension. Plantaris muscle-to-body weight (mg/g) ratio decreased 17% from Con with Sus but returned to Con with 12-h Reload, increasing 13% from Sus. Sus decreased RhoA protein concentration 46%, whereas 12-h Reload induced a 24% increase compared with Sus. The ratio of cytosolic- to membrane-associated RhoA protein was not changed with either Sus or 12-h Reload. RhoA mRNA concentration was decreased 48% by Sus, and 12-h Reload induced a 170% increase from Sus. β1-Integrin protein, a transmembrane protein associated with RhoA activation, was not altered by Sus but increased 155% with 12-h Reload. Although β1-integrin mRNA was not altered by Sus, it increased 70% from Con with 12-h Reload. Rho family member Cdc42 protein associated with the muscle membrane was decreased 60% with Sus, and 12-h Reload induced a 172% increase compared with Sus. In conclusion, decreased RhoA protein expression and mRNA abundance are early adaptations to disuse but recover rapidly after normal locomotion is resumed.Keywords
This publication has 42 references indexed in Scilit:
- Temporal alterations in protein signaling cascades during recovery from muscle atrophyAmerican Journal of Physiology-Cell Physiology, 2003
- A novel pathway regulating the mammalian target of rapamycin (mTOR) signalingBiochemical Pharmacology, 2002
- Dystrophin-glycoprotein complex and Ras and Rho GTPase signaling are altered in muscle atrophyAmerican Journal of Physiology-Cell Physiology, 2002
- Inhibiting Bacteria and Skin pH in HemiplegiaAmerican Journal of Physical Medicine & Rehabilitation, 2002
- Rho signals to cell growth and apoptosisCancer Letters, 2001
- Cytoskeletal protein contents before and after hindlimb suspension in a fast and slow rat skeletal muscleAmerican Journal of Physiology-Regulatory, Integrative and Comparative Physiology, 2001
- Rho Family Small G Proteins Play Critical Roles in Mechanical Stress–Induced Hypertrophic Responses in Cardiac MyocytesCirculation Research, 1999
- Phosphorylation of p70S6kcorrelates with increased skeletal muscle mass following resistance exerciseAmerican Journal of Physiology-Cell Physiology, 1999
- RhoA GTPase and Serum Response Factor Control Selectively the Expression of MyoD without Affecting Myf5 in Mouse MyoblastsMolecular Biology of the Cell, 1998
- Regulation of skeletal alpha-actin promoter in young chickens during hypertrophy caused by stretch overloadAmerican Journal of Physiology-Cell Physiology, 1995