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Increased Angiogenesis and Lymphangiogenesis in the Placental Villi of Women with Chronic Venous Disease during Pregnancy
Pregnancy is a period in a woman’s life associated with an increased risk of developing lower extremity chronic venous disease (CVD). Pregnancy-associated CVD is associated with changes in placental villi. We investigated angiogenesis and lymphangiogenesis in the placental villi of women with CVD du...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7177264/ https://www.ncbi.nlm.nih.gov/pubmed/32260158 http://dx.doi.org/10.3390/ijms21072487 |
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author | Ortega, Miguel A Saez, Miguel A Fraile-Martínez, Oscar Asúnsolo, Ángel Pekarek, Leonel Bravo, Coral Coca, Santiago Sainz, Felipe Mon, Melchor Álvarez- Buján, Julia García-Honduvilla, Natalio |
author_facet | Ortega, Miguel A Saez, Miguel A Fraile-Martínez, Oscar Asúnsolo, Ángel Pekarek, Leonel Bravo, Coral Coca, Santiago Sainz, Felipe Mon, Melchor Álvarez- Buján, Julia García-Honduvilla, Natalio |
author_sort | Ortega, Miguel A |
collection | PubMed |
description | Pregnancy is a period in a woman’s life associated with an increased risk of developing lower extremity chronic venous disease (CVD). Pregnancy-associated CVD is associated with changes in placental villi. We investigated angiogenesis and lymphangiogenesis in the placental villi of women with CVD during pregnancy compared with healthy controls with no history of CVD (HC). An observational, analytical, and prospective cohort study was conducted on 114 women in their third trimester of pregnancy (32 weeks). Sixty-two participants were clinically diagnosed with CVD. In parallel, 52 controls with no history of CVD (HC) were studied. Gene and protein expression of CD31, podoplanin (D2-40), Flt-1, and placental growth factor (PIGF) was analysed by real-time polymerase chain reaction (RT-qPCR) and immunohistochemistry. CD31 and D2-40 gene expression was significantly greater in the placental villi of women with CVD, as were the numbers of vessels positive for CD31 and D2-40. Significantly higher gene and protein expression of Flt-1 and PIGF was observed in the placental villi of women with CVD. Histological analysis showed more placental villi with periodic acid of Schiff (PAS)-positive material in women with CVD. Our results show a connection between pregnancy-associated CVD and leading to higher proangiogenic and lymphangiogenic activity in placental villi. |
format | Online Article Text |
id | pubmed-7177264 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-71772642020-04-28 Increased Angiogenesis and Lymphangiogenesis in the Placental Villi of Women with Chronic Venous Disease during Pregnancy Ortega, Miguel A Saez, Miguel A Fraile-Martínez, Oscar Asúnsolo, Ángel Pekarek, Leonel Bravo, Coral Coca, Santiago Sainz, Felipe Mon, Melchor Álvarez- Buján, Julia García-Honduvilla, Natalio Int J Mol Sci Article Pregnancy is a period in a woman’s life associated with an increased risk of developing lower extremity chronic venous disease (CVD). Pregnancy-associated CVD is associated with changes in placental villi. We investigated angiogenesis and lymphangiogenesis in the placental villi of women with CVD during pregnancy compared with healthy controls with no history of CVD (HC). An observational, analytical, and prospective cohort study was conducted on 114 women in their third trimester of pregnancy (32 weeks). Sixty-two participants were clinically diagnosed with CVD. In parallel, 52 controls with no history of CVD (HC) were studied. Gene and protein expression of CD31, podoplanin (D2-40), Flt-1, and placental growth factor (PIGF) was analysed by real-time polymerase chain reaction (RT-qPCR) and immunohistochemistry. CD31 and D2-40 gene expression was significantly greater in the placental villi of women with CVD, as were the numbers of vessels positive for CD31 and D2-40. Significantly higher gene and protein expression of Flt-1 and PIGF was observed in the placental villi of women with CVD. Histological analysis showed more placental villi with periodic acid of Schiff (PAS)-positive material in women with CVD. Our results show a connection between pregnancy-associated CVD and leading to higher proangiogenic and lymphangiogenic activity in placental villi. MDPI 2020-04-03 /pmc/articles/PMC7177264/ /pubmed/32260158 http://dx.doi.org/10.3390/ijms21072487 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Ortega, Miguel A Saez, Miguel A Fraile-Martínez, Oscar Asúnsolo, Ángel Pekarek, Leonel Bravo, Coral Coca, Santiago Sainz, Felipe Mon, Melchor Álvarez- Buján, Julia García-Honduvilla, Natalio Increased Angiogenesis and Lymphangiogenesis in the Placental Villi of Women with Chronic Venous Disease during Pregnancy |
title | Increased Angiogenesis and Lymphangiogenesis in the Placental Villi of Women with Chronic Venous Disease during Pregnancy |
title_full | Increased Angiogenesis and Lymphangiogenesis in the Placental Villi of Women with Chronic Venous Disease during Pregnancy |
title_fullStr | Increased Angiogenesis and Lymphangiogenesis in the Placental Villi of Women with Chronic Venous Disease during Pregnancy |
title_full_unstemmed | Increased Angiogenesis and Lymphangiogenesis in the Placental Villi of Women with Chronic Venous Disease during Pregnancy |
title_short | Increased Angiogenesis and Lymphangiogenesis in the Placental Villi of Women with Chronic Venous Disease during Pregnancy |
title_sort | increased angiogenesis and lymphangiogenesis in the placental villi of women with chronic venous disease during pregnancy |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7177264/ https://www.ncbi.nlm.nih.gov/pubmed/32260158 http://dx.doi.org/10.3390/ijms21072487 |
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