Sg. Finn et al., G alpha(13) stimulates gene expression and increases cell size in culturedneonatal rat ventricular myocytes, CARDIO RES, 42(1), 1999, pp. 140-148
Citations number
61
Categorie Soggetti
Cardiovascular & Respiratory Systems","Cardiovascular & Hematology Research
Objectives: Constitutively-active Ga,, causes permissive cell types to prol
iferate or undergo phenotypic transformation implying a role for G(13) in t
he control of cell growth. Cardiac myocytes are terminally-differentiated c
ells which respond to growth stimuli by increasing in size rather than by c
ell division. The objective of this study was to determine whether constitu
tively-active G alpha(13) is able to induce a hypertrophic phenotype in car
diac myocytes. Methods: Cultured neonatal rat ventricular myocytes were tra
nsiently transfected with an expression vector (pRC/RSV) encoding wild-type
G alpha(13) or constitutively-active G(alpha 13)Q226L. Effects on transcri
ption were monitored by co-transfected luciferase (LUX) reporter genes unde
r the control of promoters responsive to hypertrophic stimuli. Cell size wa
s determined by planimetry. Results: Transfection of neonatal myocytes with
G alpha(13)Q226L, but not wild-type G alpha(13), stimulated ANF638LUX and
ANF3003LUX expression to 3.0+/-0.3- and 4.3+/-0.6-fold of the control, resp
ectively. Likewise, G alpha(12)Q226L stimulated vMLC250LUX and vMLC2700LUX
expression to 3.9+/-1.0- and to 7.7+/-1.7-fold of controls, respectively, b
ut there was relatively little effect of G alpha(13)Q226L on c-fos-SRE- and
beta-MHC promoter activity. The effects of G alpha(13)Q226L on ANF3003LUX
were inhibited by expression of C3 exoenzyme. Wild-type G alpha(13) and G a
lpha(13)Q226L increased myocyte area from 869+/-43 mu m(2) in control trans
fections to 1287+/-64 mu m(2) and 1278+/-59 mu m(2), respectively. Conclusi
on: We conclude that G alpha(13)Q226L is able to induce gene expression and
morphological changes associated with a hypertrophic response in cardiac m
yocytes and that the transcriptional effects may be mediated through a Rho-
dependent mechanism. (C) 1999 Elsevier Science B.V. All rights reserved.