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Reporting of sex as a variable in cardiovascular studies using cultured cells

BACKGROUND: Chromosomal complement, including that provided by the sex chromosomes, influences expression of proteins and molecular signaling in every cell. However, less than 50% of the scientific studies published in 2009 using experimental animals reported sex as a biological variable. Because ev...

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Autores principales: Taylor, K Efua, Vallejo-Giraldo, Catalina, Schaible, Niccole S, Zakeri, Rosita, Miller, Virginia M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3224776/
https://www.ncbi.nlm.nih.gov/pubmed/22060014
http://dx.doi.org/10.1186/2042-6410-2-11
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author Taylor, K Efua
Vallejo-Giraldo, Catalina
Schaible, Niccole S
Zakeri, Rosita
Miller, Virginia M
author_facet Taylor, K Efua
Vallejo-Giraldo, Catalina
Schaible, Niccole S
Zakeri, Rosita
Miller, Virginia M
author_sort Taylor, K Efua
collection PubMed
description BACKGROUND: Chromosomal complement, including that provided by the sex chromosomes, influences expression of proteins and molecular signaling in every cell. However, less than 50% of the scientific studies published in 2009 using experimental animals reported sex as a biological variable. Because every cell has a sex, we conducted a literature review to determine the extent to which sex is reported as a variable in cardiovascular studies on cultured cells. METHODS: Articles from 10 cardiovascular journals with high impact factors (Circulation, J Am Coll Cardiol, Eur Heart J, Circ Res, Arterioscler Thromb Vasc Biol, Cardiovasc Res, J Mol Cell Cardiol, Am J Physiol Heart Circ Physiol, J Heart Lung Transplant and J Cardiovasc Pharmacol) and published in 2010 were searched using terms 'cultured' and 'cells' in any order to determine if the sex of those cells was reported. Studies using established cell lines were excluded. RESULTS: Using two separate search strategies, we found that only 25 of 90 articles (28%) and 20 of 101 articles (19.8%) reported the sex of cells. Of those reporting the sex of cells, most (68.9%; n = 31) used only male cells and none used exclusively female cells. In studies reporting the sex of cells of cardiovascular origin, 40% used vascular smooth-muscle cells, and 30% used stem/progenitor cells. In studies using cells of human origin, 35% did not report the sex of those cells. None of the studies using neonatal cardiac myocytes reported the sex of those cells. CONCLUSIONS: The complement of sex chromosomes in cells studied in culture has the potential to affect expression of proteins and 'mechanistic' signaling pathways. Therefore, consistent with scientific excellence, editorial policies should require reporting sex of cells used in in vitro experiments.
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spelling pubmed-32247762011-11-28 Reporting of sex as a variable in cardiovascular studies using cultured cells Taylor, K Efua Vallejo-Giraldo, Catalina Schaible, Niccole S Zakeri, Rosita Miller, Virginia M Biol Sex Differ Research BACKGROUND: Chromosomal complement, including that provided by the sex chromosomes, influences expression of proteins and molecular signaling in every cell. However, less than 50% of the scientific studies published in 2009 using experimental animals reported sex as a biological variable. Because every cell has a sex, we conducted a literature review to determine the extent to which sex is reported as a variable in cardiovascular studies on cultured cells. METHODS: Articles from 10 cardiovascular journals with high impact factors (Circulation, J Am Coll Cardiol, Eur Heart J, Circ Res, Arterioscler Thromb Vasc Biol, Cardiovasc Res, J Mol Cell Cardiol, Am J Physiol Heart Circ Physiol, J Heart Lung Transplant and J Cardiovasc Pharmacol) and published in 2010 were searched using terms 'cultured' and 'cells' in any order to determine if the sex of those cells was reported. Studies using established cell lines were excluded. RESULTS: Using two separate search strategies, we found that only 25 of 90 articles (28%) and 20 of 101 articles (19.8%) reported the sex of cells. Of those reporting the sex of cells, most (68.9%; n = 31) used only male cells and none used exclusively female cells. In studies reporting the sex of cells of cardiovascular origin, 40% used vascular smooth-muscle cells, and 30% used stem/progenitor cells. In studies using cells of human origin, 35% did not report the sex of those cells. None of the studies using neonatal cardiac myocytes reported the sex of those cells. CONCLUSIONS: The complement of sex chromosomes in cells studied in culture has the potential to affect expression of proteins and 'mechanistic' signaling pathways. Therefore, consistent with scientific excellence, editorial policies should require reporting sex of cells used in in vitro experiments. BioMed Central 2011-11-07 /pmc/articles/PMC3224776/ /pubmed/22060014 http://dx.doi.org/10.1186/2042-6410-2-11 Text en Copyright ©2011 Taylor et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Taylor, K Efua
Vallejo-Giraldo, Catalina
Schaible, Niccole S
Zakeri, Rosita
Miller, Virginia M
Reporting of sex as a variable in cardiovascular studies using cultured cells
title Reporting of sex as a variable in cardiovascular studies using cultured cells
title_full Reporting of sex as a variable in cardiovascular studies using cultured cells
title_fullStr Reporting of sex as a variable in cardiovascular studies using cultured cells
title_full_unstemmed Reporting of sex as a variable in cardiovascular studies using cultured cells
title_short Reporting of sex as a variable in cardiovascular studies using cultured cells
title_sort reporting of sex as a variable in cardiovascular studies using cultured cells
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3224776/
https://www.ncbi.nlm.nih.gov/pubmed/22060014
http://dx.doi.org/10.1186/2042-6410-2-11
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