P. Pacaud et al., ATP RAISES [CA2-2-RECEPTOR SUBTYPES IN FRESHLY ISOLATED AND CULTURED AORTIC MYOCYTES(](I) VIA DIFFERENT P), American journal of physiology. Heart and circulatory physiology, 38(1), 1995, pp. 30-36
In vascular smooth muscle, extracellular ATP induces an increase in in
tracellular [Ca2+] ([Ca2+](i)). Various agonists have been used to cha
racterize P-2-purinoeeptor subtypes involved in the ATP-induced [Ca2+]
(i) rise, measured by indo 1 fluorescence, in both freshly isolated an
d cultured rat aortic smooth muscle cells. alpha,beta-Methylene-ATP in
creased [Ca2+](i) via Ca2+ entry through P-2x-receptor channels in fre
shly isolated but not in cultured cells. 2-Methylthio-ATP and ADP fail
ed to release Ca2+ via P-2y-receptor activation in freshly isolated ce
lls, whereas such a response was obtained in cultured cells. UTP, by s
timulating P-2u receptors, released Ca2+ from intracellular stores in
both freshly isolated and cultured cells. These results suggest that,
in the course of the culture process, P-2x-receptor activation-induced
responses were lost, whereas P-2y-receptor activation-induced [Ca2+](
i) rise appeared, these two phenomena being independent. Responses to
P-2x-receptor agonist were lost in all culture conditions, whereas fun
ctional P-2y receptors appeared only in cells that were stimulated wit
h serum to induce cell cycle progression. The phenotypic modulation of
vascular myocytes was therefore associated with a change in the funct
ional P-2-purinoceptor subtypes.