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Altered VEGF-stimulated Ca2+ signaling in part underlies pregnancy-adapted eNOS activity in UAEC.
Boeldt, Derek S; Grummer, Mary A; Magness, Ronald R; Bird, Ian M.
Afiliação
  • Boeldt DS; Perinatal Research LaboratoriesDepartment of Obstetrics and Gynecology, School Medicine and Public Health, University of Wisconsin-Madison, 7E Meriter Hospital/Park, 202 South Park Street, Madison, Wisconsin 53715, USADepartment of PediatricsSchool Medicine and Public HealthDepartment of Animal Scie
  • Grummer MA; Perinatal Research LaboratoriesDepartment of Obstetrics and Gynecology, School Medicine and Public Health, University of Wisconsin-Madison, 7E Meriter Hospital/Park, 202 South Park Street, Madison, Wisconsin 53715, USADepartment of PediatricsSchool Medicine and Public HealthDepartment of Animal Scie
  • Magness RR; Perinatal Research LaboratoriesDepartment of Obstetrics and Gynecology, School Medicine and Public Health, University of Wisconsin-Madison, 7E Meriter Hospital/Park, 202 South Park Street, Madison, Wisconsin 53715, USADepartment of PediatricsSchool Medicine and Public HealthDepartment of Animal Scie
  • Bird IM; Perinatal Research LaboratoriesDepartment of Obstetrics and Gynecology, School Medicine and Public Health, University of Wisconsin-Madison, 7E Meriter Hospital/Park, 202 South Park Street, Madison, Wisconsin 53715, USADepartment of PediatricsSchool Medicine and Public HealthDepartment of Animal Scie
J Endocrinol ; 223(1): 1-11, 2014 Oct.
Article em En | MEDLINE | ID: mdl-25063757
In pregnancy, the uterine vasculature undergoes dramatic vasodilatory adaptations. Previously, vascular endothelial growth factor (VEGF) has been shown to stimulate endothelial nitric oxide synthase (eNOS) in uterine artery endothelial cells (UAECs) derived from pregnant ewes to a greater extent than those from non-pregnant ewes in a manner not fully explained by changes in the phosphorylation of eNOS. In this study, we used Fura-2 Ca(2+) imaging and arginine-to-citrulline conversion eNOS activity assays to assess the importance of VEGF-stimulated Ca(2+) responses in pregnancy-related changes in NO production in UAEC. In this study, we show that pregnancy-induced changes in VEGF-stimulated Ca(2+) responses could account in part for the greater capacity of VEGF to stimulate eNOS in UAECs from pregnant versus non-pregnant animals. VEGF-stimulated Ca(2+) responses in UAECs from pregnant and non-pregnant animals were mediated through VEGF receptor 2 and were detected in roughly 15% of all cells. There were no pregnancy-specific differences in area under the curve or peak height. UAECs from pregnant animals were more consistent in the time to response initiation, had a larger component of extracellular Ca(2+) entry, and were more sensitive to a submaximal dose of VEGF. In UAECs from pregnant and non-pregnant animals Ca(2+) responses and eNOS activation were sensitive to the phospholipase C/inositol 1,4,5-trisphosphate pathway inhibitors 2-aminoethoxydiphenylborane and U73122. Thus, changes in VEGF-stimulated [Ca(2+)]i are necessary for eNOS activation in UAECs, and pregnancy-induced changes in Ca(2+) responses could also in part explain the pregnancy-specific adaptive increase in eNOS activity in UAECs.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Cálcio / Sinalização do Cálcio / Células Endoteliais / Fator A de Crescimento do Endotélio Vascular / Óxido Nítrico Sintase Tipo III Tipo de estudo: Prognostic_studies Limite: Animals / Pregnancy Idioma: En Revista: J Endocrinol Ano de publicação: 2014 Tipo de documento: Article País de publicação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Cálcio / Sinalização do Cálcio / Células Endoteliais / Fator A de Crescimento do Endotélio Vascular / Óxido Nítrico Sintase Tipo III Tipo de estudo: Prognostic_studies Limite: Animals / Pregnancy Idioma: En Revista: J Endocrinol Ano de publicação: 2014 Tipo de documento: Article País de publicação: Reino Unido