STIM 1/Orai 1 contributes to sex differences in vascular responses to calcium in spontaneously hypertensive rats


Autoria(s): Vitorino, Fernanda Regina Casagrande Giachini; Lima, Victor Vitorino; Filgueira, Fernando Paranaiba; Dorrance, Anne M.; Carvalho, Maria Helena Catelli de; Fortes, Zuleica Bruno; Webb, R. Clinton; Passaglia, Rita de Cassia Aleixo Tostes
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

01/11/2013

01/11/2013

2012

Resumo

Sex differences in Ca2+-dependent signalling and homoeostasis in the vasculature of hypertensive rats are well characterized. However, sex-related differences in SOCE (store-operated Ca2+ entry) have been minimally investigated. We hypothesized that vascular protection in females, compared with males, reflects decreased Ca2+ mobilization due to diminished activation of Orai 1/STIM 1 (stromal interaction molecule I). In addition, we investigated whether ovariectomy in females affects the activation of the Orai 1/STIM 1 pathway. Endothelium-denuded aortic rings from male and female SHRSP (stroke-prone spontaneously hypertensive rats) and WKY (Wistar Kyoto) rats and from OVX (ovariectomized) or sham female SHRSP and WKY rats were used to functionally evaluate Ca2+ influx-induced contractions. Compared with females, aorta from male SHRSP displayed: (i) increased contraction during the Ca2+-loading period; (ii) similar transient contraction during Ca2+ release from the intracellular stores; (iii) increased activation of STIM 1 and Orai1, as shown by the blockade of STIM 1 and Orai1 with neutralizing antibodies, which reversed the sex differences in contraction during the Ca2+-loading period; and (iv) increased expression of STIM I and Orai I. Additionally, we found that aortas from OVX-SHRSP showed increased contraction during the Ca2+-loading period and increased Orai1 expression, but no changes in the SR (sarcoplasmic reticulum)-buffering capacity or STIM I expression. These findings suggest that augmented activation of STIM 1/Orai 1 in aortas from male SHRSP represents a mechanism that contributes to sex-related impaired control of intracellular Ca2+ levels. Furthermore, female sex hormones may negatively modulate the STIM/Orai 1 pathway, contributing to vascular protection observed in female rats.

American Heart Association [AHA 09GRNT2250383]

American Heart Association

National Institutes of Health [NIH HL71138, DK83685]

National Institutes of Health

Society for Womens Health Research

Society for Women's Health Research

Fundacaode Amparo a Pesquisa do Estado de Sao Paulo [FAPESP 2009/08095-5]

Fundacao de Amparo a Pesquisa do Estado de Sao Paulo

Conselho Nacional de Pesquisa e Desenvolviments (CNPq)

Conselho Nacional de Pesquisa e Desenvolviments (CNPq)

Identificador

CLINICAL SCIENCE, LONDON, v. 122, n. 41430, supl. 1, Part 3, pp. 215-226, MAR, 2012

0143-5221

http://www.producao.usp.br/handle/BDPI/37513

10.1042/CS20110312

http://dx.doi.org/10.1042/CS20110312

Idioma(s)

eng

Publicador

PORTLAND PRESS LTD

LONDON

Relação

CLINICAL SCIENCE

Direitos

restrictedAccess

Copyright PORTLAND PRESS LTD

Palavras-Chave #AORTA #CALCIUM #HYPERTENSION #ORAI1 #STROMAL INTERACTION MOLECULE 1 (STIM1) #SEX DIFFERENCE #VASCULAR PROTECTION #SMOOTH-MUSCLE-CELLS #CA2+ ENTRY MECHANISMS #ANGIOTENSIN-II #GONADAL-HORMONES #CHANNEL FUNCTION #GENDER #MEMBRANE #ARTERIES #FEMALE #PRESSURE #MEDICINE, RESEARCH & EXPERIMENTAL
Tipo

article

original article

publishedVersion