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Elevated Expression of KiSS-1 in Placenta of Chinese Women with Early-Onset Preeclampsia
Preeclampsia (PE) is a heterogeneous syndrome affecting 2% to 8% of all pregnancies and is the world’s leading cause of fetal and maternal morbidity and mortality. In many cases of PE, shallow trophoblast invasion results in inappropriate maternal spiral artery remodeling and impaired placental func...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2012
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3493594/ https://www.ncbi.nlm.nih.gov/pubmed/23145030 http://dx.doi.org/10.1371/journal.pone.0048937 |
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author | Qiao, Chong Wang, Chunhui Zhao, Jiao Liu, Caixia Shang, Tao |
author_facet | Qiao, Chong Wang, Chunhui Zhao, Jiao Liu, Caixia Shang, Tao |
author_sort | Qiao, Chong |
collection | PubMed |
description | Preeclampsia (PE) is a heterogeneous syndrome affecting 2% to 8% of all pregnancies and is the world’s leading cause of fetal and maternal morbidity and mortality. In many cases of PE, shallow trophoblast invasion results in inappropriate maternal spiral artery remodeling and impaired placental function. Multiple genes have been implicated in trophoblast invasion, among which are KiSS-1 and GPR54. The gene product of KiSS-1 is metastin, which is a ligand for the receptor GPR54. Both metastin and GPR54 are expressed in the placenta of normal pregnancy and have been implicated in modulating trophoblast invasion through inhibiting migration of trophoblast cells. We have previously reported that the expression level of KiSS-1 was higher in trophoblasts from women with preeclampsia as compared to normal controls. Here, using quantitative RT-PCR, Western blot analysis and immunohistochemistry, we extend our analysis to demonstrate that elevated KiSS-1 expression occurs only in early-onset preeclampsia (ePE) and not late-onset preeclampsia (lPE). However, no difference in the expression levels of GPR54 is observed between ePE, lPE, and normal controls. Further, we show that KiSS-1 expression is also increased in placenta of intrauterine death and birth asphyxia in comparison to normal newborns of ePE and lPE. Our findings suggest that aberrant upregulation of KiSS-1 expression may contribute to the underlying mechanism of ePE as well as birth asphyxia. |
format | Online Article Text |
id | pubmed-3493594 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-34935942012-11-09 Elevated Expression of KiSS-1 in Placenta of Chinese Women with Early-Onset Preeclampsia Qiao, Chong Wang, Chunhui Zhao, Jiao Liu, Caixia Shang, Tao PLoS One Research Article Preeclampsia (PE) is a heterogeneous syndrome affecting 2% to 8% of all pregnancies and is the world’s leading cause of fetal and maternal morbidity and mortality. In many cases of PE, shallow trophoblast invasion results in inappropriate maternal spiral artery remodeling and impaired placental function. Multiple genes have been implicated in trophoblast invasion, among which are KiSS-1 and GPR54. The gene product of KiSS-1 is metastin, which is a ligand for the receptor GPR54. Both metastin and GPR54 are expressed in the placenta of normal pregnancy and have been implicated in modulating trophoblast invasion through inhibiting migration of trophoblast cells. We have previously reported that the expression level of KiSS-1 was higher in trophoblasts from women with preeclampsia as compared to normal controls. Here, using quantitative RT-PCR, Western blot analysis and immunohistochemistry, we extend our analysis to demonstrate that elevated KiSS-1 expression occurs only in early-onset preeclampsia (ePE) and not late-onset preeclampsia (lPE). However, no difference in the expression levels of GPR54 is observed between ePE, lPE, and normal controls. Further, we show that KiSS-1 expression is also increased in placenta of intrauterine death and birth asphyxia in comparison to normal newborns of ePE and lPE. Our findings suggest that aberrant upregulation of KiSS-1 expression may contribute to the underlying mechanism of ePE as well as birth asphyxia. Public Library of Science 2012-11-08 /pmc/articles/PMC3493594/ /pubmed/23145030 http://dx.doi.org/10.1371/journal.pone.0048937 Text en © 2012 Qiao et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Qiao, Chong Wang, Chunhui Zhao, Jiao Liu, Caixia Shang, Tao Elevated Expression of KiSS-1 in Placenta of Chinese Women with Early-Onset Preeclampsia |
title | Elevated Expression of KiSS-1 in Placenta of Chinese Women with Early-Onset Preeclampsia |
title_full | Elevated Expression of KiSS-1 in Placenta of Chinese Women with Early-Onset Preeclampsia |
title_fullStr | Elevated Expression of KiSS-1 in Placenta of Chinese Women with Early-Onset Preeclampsia |
title_full_unstemmed | Elevated Expression of KiSS-1 in Placenta of Chinese Women with Early-Onset Preeclampsia |
title_short | Elevated Expression of KiSS-1 in Placenta of Chinese Women with Early-Onset Preeclampsia |
title_sort | elevated expression of kiss-1 in placenta of chinese women with early-onset preeclampsia |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3493594/ https://www.ncbi.nlm.nih.gov/pubmed/23145030 http://dx.doi.org/10.1371/journal.pone.0048937 |
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