Cargando…
Comparison in gene expression of secretory human endometrium using laser microdissection
BACKGROUND: The endometrium prepares for implantation under the control of steroid hormones. It has been suggested that there are complicated interactions between the epithelium and stroma in the endometrium during menstrual cycle. In this study, we demonstrate a difference in gene expression betwee...
Autores principales: | , , , , , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2004
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC520833/ https://www.ncbi.nlm.nih.gov/pubmed/15373944 http://dx.doi.org/10.1186/1477-7827-2-66 |
_version_ | 1782121821607297024 |
---|---|
author | Yanaihara, Atsushi Otsuka, Yukiko Iwasaki, Shinji Koide, Keiko Aida, Tadateru Okai, Takashi |
author_facet | Yanaihara, Atsushi Otsuka, Yukiko Iwasaki, Shinji Koide, Keiko Aida, Tadateru Okai, Takashi |
author_sort | Yanaihara, Atsushi |
collection | PubMed |
description | BACKGROUND: The endometrium prepares for implantation under the control of steroid hormones. It has been suggested that there are complicated interactions between the epithelium and stroma in the endometrium during menstrual cycle. In this study, we demonstrate a difference in gene expression between the epithelial and stromal areas of the secretory human endometrium using microdissection and macroarray technique. METHODS: The epithelial and stromal areas were microdissected from the human endometrium during the secretory phase. RNA was extracted and amplified by PCR. Macroarray analysis of nearly 1000 human genes was carried out in this study. Some genes identified by macroarray analysis were verified using real-time PCR. RESULTS: In this study, changes in expression <2.5-fold in three samples were excluded. A total of 28 genes displayed changes in expression from array data. Fifteen genes were strongly expressed in the epithelial areas, while 13 genes were strongly expressed in the stromal areas. The strongly expressed genes in the epithelial areas with a changes >5-fold were WAP four-disulfide core domain 2 (44.1 fold), matrix metalloproteinase 7 (40.1 fold), homeo box B5 (19.8 fold), msh homeo box homolog (18.8 fold), homeo box B7 (12.7 fold) and protein kinase C, theta (6.4 fold). On the other hand, decorin (55.6 fold), discoidin domain receptor member 2 (17.3 fold), tissue inhibitor of metalloproteinase 1 (9 fold), ribosomal protein S3A (6.3 fold), and tyrosine kinase with immunoglobulin and epidermal growth factor homology domains (5.2 fold) were strongly expressed in the stromal areas. WAP four-disulfide core domain 2 (19.4 fold), matrix metalloproteinase 7 (9.7-fold), decorin (16.3-fold) and tissue inhibitor of metalloproteinase 1 (7.2-fold) were verified by real-time PCR. CONCLUSIONS: Some of the genes we identified with differential expression are related to the immune system. These results are telling us the new information for understanding the secretory human endometrium. |
format | Text |
id | pubmed-520833 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2004 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-5208332004-10-01 Comparison in gene expression of secretory human endometrium using laser microdissection Yanaihara, Atsushi Otsuka, Yukiko Iwasaki, Shinji Koide, Keiko Aida, Tadateru Okai, Takashi Reprod Biol Endocrinol Research BACKGROUND: The endometrium prepares for implantation under the control of steroid hormones. It has been suggested that there are complicated interactions between the epithelium and stroma in the endometrium during menstrual cycle. In this study, we demonstrate a difference in gene expression between the epithelial and stromal areas of the secretory human endometrium using microdissection and macroarray technique. METHODS: The epithelial and stromal areas were microdissected from the human endometrium during the secretory phase. RNA was extracted and amplified by PCR. Macroarray analysis of nearly 1000 human genes was carried out in this study. Some genes identified by macroarray analysis were verified using real-time PCR. RESULTS: In this study, changes in expression <2.5-fold in three samples were excluded. A total of 28 genes displayed changes in expression from array data. Fifteen genes were strongly expressed in the epithelial areas, while 13 genes were strongly expressed in the stromal areas. The strongly expressed genes in the epithelial areas with a changes >5-fold were WAP four-disulfide core domain 2 (44.1 fold), matrix metalloproteinase 7 (40.1 fold), homeo box B5 (19.8 fold), msh homeo box homolog (18.8 fold), homeo box B7 (12.7 fold) and protein kinase C, theta (6.4 fold). On the other hand, decorin (55.6 fold), discoidin domain receptor member 2 (17.3 fold), tissue inhibitor of metalloproteinase 1 (9 fold), ribosomal protein S3A (6.3 fold), and tyrosine kinase with immunoglobulin and epidermal growth factor homology domains (5.2 fold) were strongly expressed in the stromal areas. WAP four-disulfide core domain 2 (19.4 fold), matrix metalloproteinase 7 (9.7-fold), decorin (16.3-fold) and tissue inhibitor of metalloproteinase 1 (7.2-fold) were verified by real-time PCR. CONCLUSIONS: Some of the genes we identified with differential expression are related to the immune system. These results are telling us the new information for understanding the secretory human endometrium. BioMed Central 2004-09-17 /pmc/articles/PMC520833/ /pubmed/15373944 http://dx.doi.org/10.1186/1477-7827-2-66 Text en Copyright © 2004 Yanaihara 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 Yanaihara, Atsushi Otsuka, Yukiko Iwasaki, Shinji Koide, Keiko Aida, Tadateru Okai, Takashi Comparison in gene expression of secretory human endometrium using laser microdissection |
title | Comparison in gene expression of secretory human endometrium using laser microdissection |
title_full | Comparison in gene expression of secretory human endometrium using laser microdissection |
title_fullStr | Comparison in gene expression of secretory human endometrium using laser microdissection |
title_full_unstemmed | Comparison in gene expression of secretory human endometrium using laser microdissection |
title_short | Comparison in gene expression of secretory human endometrium using laser microdissection |
title_sort | comparison in gene expression of secretory human endometrium using laser microdissection |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC520833/ https://www.ncbi.nlm.nih.gov/pubmed/15373944 http://dx.doi.org/10.1186/1477-7827-2-66 |
work_keys_str_mv | AT yanaiharaatsushi comparisoningeneexpressionofsecretoryhumanendometriumusinglasermicrodissection AT otsukayukiko comparisoningeneexpressionofsecretoryhumanendometriumusinglasermicrodissection AT iwasakishinji comparisoningeneexpressionofsecretoryhumanendometriumusinglasermicrodissection AT koidekeiko comparisoningeneexpressionofsecretoryhumanendometriumusinglasermicrodissection AT aidatadateru comparisoningeneexpressionofsecretoryhumanendometriumusinglasermicrodissection AT okaitakashi comparisoningeneexpressionofsecretoryhumanendometriumusinglasermicrodissection |