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STIM and Orai isoform expression in pregnant human myometrium: a potential role in calcium signaling during pregnancy

Store-operated calcium (Ca(2+)) entry (SOCE) can be mediated by two novel proteins, STIM/Orai. We have previously demonstrated that members of the TRPC family, putative basal and store operated calcium entry channels, are present in human myometrium and regulated by labor associated stimuli IL-1β an...

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Autores principales: Chin-Smith, Evonne C., Slater, Donna M., Johnson, Mark R., Tribe, Rachel M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4018559/
https://www.ncbi.nlm.nih.gov/pubmed/24834055
http://dx.doi.org/10.3389/fphys.2014.00169
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author Chin-Smith, Evonne C.
Slater, Donna M.
Johnson, Mark R.
Tribe, Rachel M.
author_facet Chin-Smith, Evonne C.
Slater, Donna M.
Johnson, Mark R.
Tribe, Rachel M.
author_sort Chin-Smith, Evonne C.
collection PubMed
description Store-operated calcium (Ca(2+)) entry (SOCE) can be mediated by two novel proteins, STIM/Orai. We have previously demonstrated that members of the TRPC family, putative basal and store operated calcium entry channels, are present in human myometrium and regulated by labor associated stimuli IL-1β and mechanical stretch. Although STIM and Orai isoforms (1-3) have been reported in other smooth muscle cell types, there is little known about the expression or gestational regulation of STIM and Orai expression in human myometrium. Total RNA was isolated from lower segment human myometrial biopsies obtained at Cesarean section from women at the time of preterm no labor (PTNL), preterm labor (PTL), term non-labor (TNL), and term with labor (TL); primary cultured human uterine smooth muscle cells, and a human myometrial cell line (hTERT-HM). STIM1-2, and Orai1-3 mRNA expression was assessed by quantitative real-time PCR. All five genes were expressed in myometrial tissue and cultured cells. STIM1-2 and Orai2-3 expression was significantly lower in cultured cells compared tissue. This has implications with regard investigation of the contribution of these proteins in cultured cells. Orai2 was the most abundant Orai isoform in human myometrium. Expression of STIM1-2/Orai1-3 did not alter with the onset of labor. Orai1 mRNA expression in cultured cells was enhanced by IL-1β treatment. This novel report of STIM1-2 and Orai1-3 mRNA expression in pregnant human myometrium and Orai1 regulation by IL-1β indicates a potential role for these proteins in calcium signaling in human myometrium during pregnancy.
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spelling pubmed-40185592014-05-15 STIM and Orai isoform expression in pregnant human myometrium: a potential role in calcium signaling during pregnancy Chin-Smith, Evonne C. Slater, Donna M. Johnson, Mark R. Tribe, Rachel M. Front Physiol Physiology Store-operated calcium (Ca(2+)) entry (SOCE) can be mediated by two novel proteins, STIM/Orai. We have previously demonstrated that members of the TRPC family, putative basal and store operated calcium entry channels, are present in human myometrium and regulated by labor associated stimuli IL-1β and mechanical stretch. Although STIM and Orai isoforms (1-3) have been reported in other smooth muscle cell types, there is little known about the expression or gestational regulation of STIM and Orai expression in human myometrium. Total RNA was isolated from lower segment human myometrial biopsies obtained at Cesarean section from women at the time of preterm no labor (PTNL), preterm labor (PTL), term non-labor (TNL), and term with labor (TL); primary cultured human uterine smooth muscle cells, and a human myometrial cell line (hTERT-HM). STIM1-2, and Orai1-3 mRNA expression was assessed by quantitative real-time PCR. All five genes were expressed in myometrial tissue and cultured cells. STIM1-2 and Orai2-3 expression was significantly lower in cultured cells compared tissue. This has implications with regard investigation of the contribution of these proteins in cultured cells. Orai2 was the most abundant Orai isoform in human myometrium. Expression of STIM1-2/Orai1-3 did not alter with the onset of labor. Orai1 mRNA expression in cultured cells was enhanced by IL-1β treatment. This novel report of STIM1-2 and Orai1-3 mRNA expression in pregnant human myometrium and Orai1 regulation by IL-1β indicates a potential role for these proteins in calcium signaling in human myometrium during pregnancy. Frontiers Media S.A. 2014-05-06 /pmc/articles/PMC4018559/ /pubmed/24834055 http://dx.doi.org/10.3389/fphys.2014.00169 Text en Copyright © 2014 Chin-Smith, Slater, Johnson and Tribe. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Physiology
Chin-Smith, Evonne C.
Slater, Donna M.
Johnson, Mark R.
Tribe, Rachel M.
STIM and Orai isoform expression in pregnant human myometrium: a potential role in calcium signaling during pregnancy
title STIM and Orai isoform expression in pregnant human myometrium: a potential role in calcium signaling during pregnancy
title_full STIM and Orai isoform expression in pregnant human myometrium: a potential role in calcium signaling during pregnancy
title_fullStr STIM and Orai isoform expression in pregnant human myometrium: a potential role in calcium signaling during pregnancy
title_full_unstemmed STIM and Orai isoform expression in pregnant human myometrium: a potential role in calcium signaling during pregnancy
title_short STIM and Orai isoform expression in pregnant human myometrium: a potential role in calcium signaling during pregnancy
title_sort stim and orai isoform expression in pregnant human myometrium: a potential role in calcium signaling during pregnancy
topic Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4018559/
https://www.ncbi.nlm.nih.gov/pubmed/24834055
http://dx.doi.org/10.3389/fphys.2014.00169
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