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Establishment of an immortalized human endometrial stromal cell line with functional responses to ovarian stimuli
Studies on the mechanisms of decidualization and endometriosis are often hampered by lack of primary endometrial cells. To facilitate in vitro studies, we established a human endometrial stromal cell line, KC02-44D, immortalized with human telomerase reverse transcriptase. Upon exposure to ovarian s...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3160358/ https://www.ncbi.nlm.nih.gov/pubmed/21801462 http://dx.doi.org/10.1186/1477-7827-9-104 |
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author | Yuhki, Munehiro Kajitani, Takashi Mizuno, Takakazu Aoki, Yuko Maruyama, Tetsuo |
author_facet | Yuhki, Munehiro Kajitani, Takashi Mizuno, Takakazu Aoki, Yuko Maruyama, Tetsuo |
author_sort | Yuhki, Munehiro |
collection | PubMed |
description | Studies on the mechanisms of decidualization and endometriosis are often hampered by lack of primary endometrial cells. To facilitate in vitro studies, we established a human endometrial stromal cell line, KC02-44D, immortalized with human telomerase reverse transcriptase. Upon exposure to ovarian stimuli, KC02-44D cells showed similar cytoskeletal marker or gene expression and biochemical phenotype to primary endometrial stromal cells. KC02-44D would be useful for studies of human endometrial function and its associated pathologies. |
format | Online Article Text |
id | pubmed-3160358 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-31603582011-08-24 Establishment of an immortalized human endometrial stromal cell line with functional responses to ovarian stimuli Yuhki, Munehiro Kajitani, Takashi Mizuno, Takakazu Aoki, Yuko Maruyama, Tetsuo Reprod Biol Endocrinol Methodology Studies on the mechanisms of decidualization and endometriosis are often hampered by lack of primary endometrial cells. To facilitate in vitro studies, we established a human endometrial stromal cell line, KC02-44D, immortalized with human telomerase reverse transcriptase. Upon exposure to ovarian stimuli, KC02-44D cells showed similar cytoskeletal marker or gene expression and biochemical phenotype to primary endometrial stromal cells. KC02-44D would be useful for studies of human endometrial function and its associated pathologies. BioMed Central 2011-08-01 /pmc/articles/PMC3160358/ /pubmed/21801462 http://dx.doi.org/10.1186/1477-7827-9-104 Text en Copyright ©2011 Yuhki 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 | Methodology Yuhki, Munehiro Kajitani, Takashi Mizuno, Takakazu Aoki, Yuko Maruyama, Tetsuo Establishment of an immortalized human endometrial stromal cell line with functional responses to ovarian stimuli |
title | Establishment of an immortalized human endometrial stromal cell line with functional responses to ovarian stimuli |
title_full | Establishment of an immortalized human endometrial stromal cell line with functional responses to ovarian stimuli |
title_fullStr | Establishment of an immortalized human endometrial stromal cell line with functional responses to ovarian stimuli |
title_full_unstemmed | Establishment of an immortalized human endometrial stromal cell line with functional responses to ovarian stimuli |
title_short | Establishment of an immortalized human endometrial stromal cell line with functional responses to ovarian stimuli |
title_sort | establishment of an immortalized human endometrial stromal cell line with functional responses to ovarian stimuli |
topic | Methodology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3160358/ https://www.ncbi.nlm.nih.gov/pubmed/21801462 http://dx.doi.org/10.1186/1477-7827-9-104 |
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