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Physical activity differentially regulates VEGF, PlGF, and their receptors in the human placenta
Physical activity (PA) has beneficial effects on the function of many organs by modulating their vascular development. Regular PA during pregnancy is associated with favorable short‐ and long‐term outcomes for both mother and fetus. During pregnancy, appropriate vascularization of the placenta is cr...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7814495/ https://www.ncbi.nlm.nih.gov/pubmed/33463910 http://dx.doi.org/10.14814/phy2.14710 |
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author | Bhattacharjee, Jayonta Mohammad, Shuhiba Goudreau, Alexandra D. Adamo, Kristi B. |
author_facet | Bhattacharjee, Jayonta Mohammad, Shuhiba Goudreau, Alexandra D. Adamo, Kristi B. |
author_sort | Bhattacharjee, Jayonta |
collection | PubMed |
description | Physical activity (PA) has beneficial effects on the function of many organs by modulating their vascular development. Regular PA during pregnancy is associated with favorable short‐ and long‐term outcomes for both mother and fetus. During pregnancy, appropriate vascularization of the placenta is crucial for adequate maternal–fetal nutrient and gas exchange. How PA modulates angiogenic factors, VEGF, and its receptors in the human placenta, is as of yet, unknown. We objectively measured the PA of women at 24–28 and 34–38 weeks of gestation. Participants were considered “active” if they had met or exceeded 150 min of moderate‐intensity PA per week during their 2nd trimester. Term placenta tissues were collected from active (n = 23) or inactive (n = 22) women immediately after delivery. We examined the expression of the angiogenic factors VEGF, PlGF, VEGFR‐1, and VEGFR‐2 in the placenta. Western blot analysis showed VEGF and its receptor, VEGFR‐1 was significantly (p < 0.05) higher both at the protein and mRNA levels in placenta from physically active compared to inactive women. No difference in VEGFR‐2 was observed. Furthermore, immunohistochemistry showed differential staining patterns of VEGF and its receptors in placental endothelial, stromal, and trophoblast cells and in the syncytial brush border. In comparison, PlGF expression did not differ either at the protein or mRNA level in the placenta from physically active or inactive women. The expression and localization pattern of VEGF and its receptors suggest that PA during pregnancy may support a pro‐angiogenic milieu to the placental vascular network. |
format | Online Article Text |
id | pubmed-7814495 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-78144952021-01-26 Physical activity differentially regulates VEGF, PlGF, and their receptors in the human placenta Bhattacharjee, Jayonta Mohammad, Shuhiba Goudreau, Alexandra D. Adamo, Kristi B. Physiol Rep Original Research Physical activity (PA) has beneficial effects on the function of many organs by modulating their vascular development. Regular PA during pregnancy is associated with favorable short‐ and long‐term outcomes for both mother and fetus. During pregnancy, appropriate vascularization of the placenta is crucial for adequate maternal–fetal nutrient and gas exchange. How PA modulates angiogenic factors, VEGF, and its receptors in the human placenta, is as of yet, unknown. We objectively measured the PA of women at 24–28 and 34–38 weeks of gestation. Participants were considered “active” if they had met or exceeded 150 min of moderate‐intensity PA per week during their 2nd trimester. Term placenta tissues were collected from active (n = 23) or inactive (n = 22) women immediately after delivery. We examined the expression of the angiogenic factors VEGF, PlGF, VEGFR‐1, and VEGFR‐2 in the placenta. Western blot analysis showed VEGF and its receptor, VEGFR‐1 was significantly (p < 0.05) higher both at the protein and mRNA levels in placenta from physically active compared to inactive women. No difference in VEGFR‐2 was observed. Furthermore, immunohistochemistry showed differential staining patterns of VEGF and its receptors in placental endothelial, stromal, and trophoblast cells and in the syncytial brush border. In comparison, PlGF expression did not differ either at the protein or mRNA level in the placenta from physically active or inactive women. The expression and localization pattern of VEGF and its receptors suggest that PA during pregnancy may support a pro‐angiogenic milieu to the placental vascular network. John Wiley and Sons Inc. 2021-01-19 /pmc/articles/PMC7814495/ /pubmed/33463910 http://dx.doi.org/10.14814/phy2.14710 Text en © 2021 The Authors. Physiological Reports published by Wiley Periodicals LLC on behalf of The Physiological Society and the American Physiological Society This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Research Bhattacharjee, Jayonta Mohammad, Shuhiba Goudreau, Alexandra D. Adamo, Kristi B. Physical activity differentially regulates VEGF, PlGF, and their receptors in the human placenta |
title | Physical activity differentially regulates VEGF, PlGF, and their receptors in the human placenta |
title_full | Physical activity differentially regulates VEGF, PlGF, and their receptors in the human placenta |
title_fullStr | Physical activity differentially regulates VEGF, PlGF, and their receptors in the human placenta |
title_full_unstemmed | Physical activity differentially regulates VEGF, PlGF, and their receptors in the human placenta |
title_short | Physical activity differentially regulates VEGF, PlGF, and their receptors in the human placenta |
title_sort | physical activity differentially regulates vegf, plgf, and their receptors in the human placenta |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7814495/ https://www.ncbi.nlm.nih.gov/pubmed/33463910 http://dx.doi.org/10.14814/phy2.14710 |
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