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Expression of Bcl-2 and p53 at the fetal-maternal interface of rhesus monkey

To study the apoptosis and its mechanism at the fetal-maternal interface of early gestation, localization of apoptotic cells in the implantation sites of the rhesus monkey on day 17, 19, 28 and 34 of pregnancy were first examine by using the TUNEL technique. The expression of Ki67, a molecular marke...

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Autores principales: Wei, Peng, Jin, Xuan, Zhang, Xue-Sen, Hu, Zhao-Yuan, Han, Chun-Sheng, Liu, Yi-Xun
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2005
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC548132/
https://www.ncbi.nlm.nih.gov/pubmed/15649334
http://dx.doi.org/10.1186/1477-7827-3-4
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author Wei, Peng
Jin, Xuan
Zhang, Xue-Sen
Hu, Zhao-Yuan
Han, Chun-Sheng
Liu, Yi-Xun
author_facet Wei, Peng
Jin, Xuan
Zhang, Xue-Sen
Hu, Zhao-Yuan
Han, Chun-Sheng
Liu, Yi-Xun
author_sort Wei, Peng
collection PubMed
description To study the apoptosis and its mechanism at the fetal-maternal interface of early gestation, localization of apoptotic cells in the implantation sites of the rhesus monkey on day 17, 19, 28 and 34 of pregnancy were first examine by using the TUNEL technique. The expression of Ki67, a molecular marker of proliferating cells, and two apoptotic proteins, B cell lymphoma/leukaemia-2 (Bcl-2) and P53, were then studied by immunohistochemistry. Apoptotic nuclei were observed mainly in the syncytiotrophoblast. Ki67 was confined almost exclusively to cytotrophoblasts. The localization of Bcl-2 protein follows that of the apoptotic nuclei and its expression level increased as the development of the placenta progressed on. P53 was detected to some extent in cytotrophoblasts and syncytiotrophoblast covering the basal feet of the anchoring villi during the late stage of placentation. Based on these observations, it might be suggested that Bcl-2 could be possible to play an interesting role in limiting degree of nuclear degradation and sustaining cell suvival in the multi-nucleated syncytiotrophoblast cells during early pregnancy, and P53 could also be essential in regulating the trophoblastic homeostasis by controlling its proliferation or apoptosis.
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spelling pubmed-5481322005-02-05 Expression of Bcl-2 and p53 at the fetal-maternal interface of rhesus monkey Wei, Peng Jin, Xuan Zhang, Xue-Sen Hu, Zhao-Yuan Han, Chun-Sheng Liu, Yi-Xun Reprod Biol Endocrinol Research To study the apoptosis and its mechanism at the fetal-maternal interface of early gestation, localization of apoptotic cells in the implantation sites of the rhesus monkey on day 17, 19, 28 and 34 of pregnancy were first examine by using the TUNEL technique. The expression of Ki67, a molecular marker of proliferating cells, and two apoptotic proteins, B cell lymphoma/leukaemia-2 (Bcl-2) and P53, were then studied by immunohistochemistry. Apoptotic nuclei were observed mainly in the syncytiotrophoblast. Ki67 was confined almost exclusively to cytotrophoblasts. The localization of Bcl-2 protein follows that of the apoptotic nuclei and its expression level increased as the development of the placenta progressed on. P53 was detected to some extent in cytotrophoblasts and syncytiotrophoblast covering the basal feet of the anchoring villi during the late stage of placentation. Based on these observations, it might be suggested that Bcl-2 could be possible to play an interesting role in limiting degree of nuclear degradation and sustaining cell suvival in the multi-nucleated syncytiotrophoblast cells during early pregnancy, and P53 could also be essential in regulating the trophoblastic homeostasis by controlling its proliferation or apoptosis. BioMed Central 2005-01-14 /pmc/articles/PMC548132/ /pubmed/15649334 http://dx.doi.org/10.1186/1477-7827-3-4 Text en Copyright © 2005 Wei 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
Wei, Peng
Jin, Xuan
Zhang, Xue-Sen
Hu, Zhao-Yuan
Han, Chun-Sheng
Liu, Yi-Xun
Expression of Bcl-2 and p53 at the fetal-maternal interface of rhesus monkey
title Expression of Bcl-2 and p53 at the fetal-maternal interface of rhesus monkey
title_full Expression of Bcl-2 and p53 at the fetal-maternal interface of rhesus monkey
title_fullStr Expression of Bcl-2 and p53 at the fetal-maternal interface of rhesus monkey
title_full_unstemmed Expression of Bcl-2 and p53 at the fetal-maternal interface of rhesus monkey
title_short Expression of Bcl-2 and p53 at the fetal-maternal interface of rhesus monkey
title_sort expression of bcl-2 and p53 at the fetal-maternal interface of rhesus monkey
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC548132/
https://www.ncbi.nlm.nih.gov/pubmed/15649334
http://dx.doi.org/10.1186/1477-7827-3-4
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