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Tubulointerstitial nephritis antigen-like 1 protein is downregulated in the placenta of pre-eclamptic women
BACKGROUND: Tubulointerstitial nephritis antigen-like 1 protein (TINAGL1), is a matricellular protein, known to play role in cell adhesion and cell receptor interaction. Research related to TINAGL1 is limited to cell culture and animal models. Demonstration of TINAGL1 as a positive regulator of angi...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5361709/ https://www.ncbi.nlm.nih.gov/pubmed/28344540 http://dx.doi.org/10.1186/s12014-017-9144-2 |
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author | Mary, Sheon Kulkarni, Mahesh J. Mehendale, Savita S. Joshi, Sadhana R. Giri, Ashok P. |
author_facet | Mary, Sheon Kulkarni, Mahesh J. Mehendale, Savita S. Joshi, Sadhana R. Giri, Ashok P. |
author_sort | Mary, Sheon |
collection | PubMed |
description | BACKGROUND: Tubulointerstitial nephritis antigen-like 1 protein (TINAGL1), is a matricellular protein, known to play role in cell adhesion and cell receptor interaction. Research related to TINAGL1 is limited to cell culture and animal models. Demonstration of TINAGL1 as a positive regulator of angiogenesis and its expression in the decidua of postimplantation mouse uterus, prompted us to validate its expression in human placenta during impaired angiogenesis in pre-eclamptic condition. METHODS: Placental tissue from normotensive (n = 25) and pre-eclamptic (n = 25) pregnancies were used to study the differentially expressed proteins by two-dimensional gel electrophoresis and TINAGL1 protein was validated with Western blotting. RESULTS: A total of 55 protein spots were differentially expressed (fold change >1.5, p < 0.05), of which 27 were upregulated and 28 were downregulated in the pre-eclamptic placenta. TINAGL1 was found to be downregulated in pre-eclamptic compared to normotensive pregnant women. CONCLUSION: This is the first study reporting TINAGL1 to be present in human placenta and differentially expressed in pre-eclamptic condition. The functional role of TINAGL1 in association to human pregnancy needs to be explored further. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12014-017-9144-2) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5361709 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-53617092017-03-24 Tubulointerstitial nephritis antigen-like 1 protein is downregulated in the placenta of pre-eclamptic women Mary, Sheon Kulkarni, Mahesh J. Mehendale, Savita S. Joshi, Sadhana R. Giri, Ashok P. Clin Proteomics Research BACKGROUND: Tubulointerstitial nephritis antigen-like 1 protein (TINAGL1), is a matricellular protein, known to play role in cell adhesion and cell receptor interaction. Research related to TINAGL1 is limited to cell culture and animal models. Demonstration of TINAGL1 as a positive regulator of angiogenesis and its expression in the decidua of postimplantation mouse uterus, prompted us to validate its expression in human placenta during impaired angiogenesis in pre-eclamptic condition. METHODS: Placental tissue from normotensive (n = 25) and pre-eclamptic (n = 25) pregnancies were used to study the differentially expressed proteins by two-dimensional gel electrophoresis and TINAGL1 protein was validated with Western blotting. RESULTS: A total of 55 protein spots were differentially expressed (fold change >1.5, p < 0.05), of which 27 were upregulated and 28 were downregulated in the pre-eclamptic placenta. TINAGL1 was found to be downregulated in pre-eclamptic compared to normotensive pregnant women. CONCLUSION: This is the first study reporting TINAGL1 to be present in human placenta and differentially expressed in pre-eclamptic condition. The functional role of TINAGL1 in association to human pregnancy needs to be explored further. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12014-017-9144-2) contains supplementary material, which is available to authorized users. BioMed Central 2017-03-21 /pmc/articles/PMC5361709/ /pubmed/28344540 http://dx.doi.org/10.1186/s12014-017-9144-2 Text en © The Author(s) 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Mary, Sheon Kulkarni, Mahesh J. Mehendale, Savita S. Joshi, Sadhana R. Giri, Ashok P. Tubulointerstitial nephritis antigen-like 1 protein is downregulated in the placenta of pre-eclamptic women |
title | Tubulointerstitial nephritis antigen-like 1 protein is downregulated in the placenta of pre-eclamptic women |
title_full | Tubulointerstitial nephritis antigen-like 1 protein is downregulated in the placenta of pre-eclamptic women |
title_fullStr | Tubulointerstitial nephritis antigen-like 1 protein is downregulated in the placenta of pre-eclamptic women |
title_full_unstemmed | Tubulointerstitial nephritis antigen-like 1 protein is downregulated in the placenta of pre-eclamptic women |
title_short | Tubulointerstitial nephritis antigen-like 1 protein is downregulated in the placenta of pre-eclamptic women |
title_sort | tubulointerstitial nephritis antigen-like 1 protein is downregulated in the placenta of pre-eclamptic women |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5361709/ https://www.ncbi.nlm.nih.gov/pubmed/28344540 http://dx.doi.org/10.1186/s12014-017-9144-2 |
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