Source:http://linkedlifedata.com/resource/pubmed/id/14668208
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
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pubmed:dateCreated |
2004-3-22
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pubmed:abstractText |
The epididymal epithelium contributes to formation of a luminal fluid that is essential for the protection of spermatozoa from a variety of insults including changes in oxygen tension. A key regulator of the response to oxygen debt in many cells is hypoxia-inducible factor-1 (HIF-1). A transcription factor composed of alpha and beta subunits, HIF-1 activates genes that mediate oxygen homeostasis and cell survival pathways or trigger cell death responses. Previously we have shown that HIF-1alpha mRNA is expressed in the adult rat epididymis. Goals of this study were to determine whether HIF-1alpha protein is activated by ischemia in the rat epididymis, to determine whether epididymal HIF-1alpha mRNA expression is androgen dependent, and to identify epididymal cell types expressing HIF-1alpha and beta. Immunoblot analysis revealed that HIF-1alpha protein is primarily present in corpus and cauda of the normoxic epididymis and unaffected by ischemia, whereas HIF-1beta was detected equally in all regions and also unaffected by ischemia. HIF-1alpha mRNA expression in all regions was not affected by 15 days bilateral orchiectomy. Principal cells stained positive for HIF-1alpha by immunocytochemistry, with the epithelium of initial segment and caput epididymidis staining less intensely than corpus and cauda. HIF-1beta immunoreactivity was equally present in principal cells in all regions. Clear, narrow, and basal cells were unreactive for HIF-1alpha and beta. The presence of HIF-1 in normoxic epididymis and the regional distribution of HIF-1alpha suggests fundamental differences in how proximal and distal regions of the epididymis maintain oxygen homeostasis to protect the epithelium and spermatozoa from hypoxia.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/ARNT protein, rat,
http://linkedlifedata.com/resource/pubmed/chemical/Aryl Hydrocarbon Receptor Nuclear...,
http://linkedlifedata.com/resource/pubmed/chemical/DNA-Binding Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Hypoxia-Inducible Factor 1, alpha...,
http://linkedlifedata.com/resource/pubmed/chemical/RNA, Messenger,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Aryl Hydrocarbon,
http://linkedlifedata.com/resource/pubmed/chemical/Testosterone,
http://linkedlifedata.com/resource/pubmed/chemical/Transcription Factors
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pubmed:status |
MEDLINE
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pubmed:month |
Apr
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pubmed:issn |
0006-3363
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
70
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1121-30
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:14668208-Animals,
pubmed-meshheading:14668208-Aryl Hydrocarbon Receptor Nuclear Translocator,
pubmed-meshheading:14668208-DNA-Binding Proteins,
pubmed-meshheading:14668208-Epididymis,
pubmed-meshheading:14668208-Hypoxia-Inducible Factor 1, alpha Subunit,
pubmed-meshheading:14668208-Immunoblotting,
pubmed-meshheading:14668208-Immunohistochemistry,
pubmed-meshheading:14668208-Ischemia,
pubmed-meshheading:14668208-Male,
pubmed-meshheading:14668208-Orchiectomy,
pubmed-meshheading:14668208-RNA, Messenger,
pubmed-meshheading:14668208-Rats,
pubmed-meshheading:14668208-Rats, Sprague-Dawley,
pubmed-meshheading:14668208-Receptors, Aryl Hydrocarbon,
pubmed-meshheading:14668208-Spermatozoa,
pubmed-meshheading:14668208-Testosterone,
pubmed-meshheading:14668208-Tissue Distribution,
pubmed-meshheading:14668208-Transcription Factors
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pubmed:year |
2004
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pubmed:articleTitle |
Expression and localization of hypoxia-inducible factor-1 subunits in the adult rat epididymis.
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pubmed:affiliation |
Department of Biology, Monmouth University, West Long Branch, New Jersey 07764, USA. mpalladi@monmouth.edu
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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