Expression of the proliferating cell nuclear antigen and protein products of tumour suppressor genes in the human foetal testis
Tumour suppressor genes retinoblastoma (Rb1) and adenomatous polyposis coli (Apc) as well as the proliferating cell nuclear antigen (PCNA) are involved in embryonic development. The purpose of the present study was to investigate the expression of Rb1 protein, APC protein and PCNA during development...
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Published in | Andrologia Vol. 36; no. 1; pp. 24 - 30 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
Berlin, Germany
Blackwell Verlag GmbH
01.02.2004
Blackwell |
Subjects | |
Online Access | Get full text |
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Summary: | Tumour suppressor genes retinoblastoma (Rb1) and adenomatous polyposis coli (Apc) as well as the proliferating cell nuclear antigen (PCNA) are involved in embryonic development. The purpose of the present study was to investigate the expression of Rb1 protein, APC protein and PCNA during development of the human foetal testis. Qualitative analysis of their expression at the single‐cell level was performed using immunohistochemistry on archive samples of the foetal testis (18–37 gestation week). Stereological parameters (volume density, absolute volume, numerical density, absolute number) were calculated for quantification of the overall expression of those proteins that were expressed frequently enough for such an analysis. PCNA was frequently expressed in nuclei of immature Sertoli cells and prospermatogonia and less frequently in surrounding peritubular (myoid) and interstitial cells. The pRb1 protein was present in nuclei of prospermatogonia and Sertoli cells but was absent from the interstitial tissue. APC protein was expressed in the cytoplasm of a very small number of prospermatogonia and interstitial (Leydig) cells. The overall expression of PCNA in all stages of development was higher than pRb1 expression. |
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Bibliography: | ark:/67375/WNG-K2ZV83ZK-R ArticleID:AND597 istex:B8BA0BADA45C325560A352A754785D3886E1EAC8 ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0303-4569 1439-0272 |
DOI: | 10.1046/j.1439-0272.2003.00597.x |