PMID- 14668208 OWN - NLM STAT- MEDLINE DCOM- 20041102 LR - 20131121 IS - 0006-3363 (Print) IS - 0006-3363 (Linking) VI - 70 IP - 4 DP - 2004 Apr TI - Expression and localization of hypoxia-inducible factor-1 subunits in the adult rat epididymis. PG - 1121-30 AB - 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. FAU - Palladino, M A AU - Palladino MA AD - Department of Biology, Monmouth University, West Long Branch, New Jersey 07764, USA. mpalladi@monmouth.edu FAU - Powell, J D AU - Powell JD FAU - Korah, N AU - Korah N FAU - Hermo, L AU - Hermo L LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20031210 PL - United States TA - Biol Reprod JT - Biology of reproduction JID - 0207224 RN - 0 (ARNT protein, rat) RN - 0 (DNA-Binding Proteins) RN - 0 (Hypoxia-Inducible Factor 1, alpha Subunit) RN - 0 (RNA, Messenger) RN - 0 (Receptors, Aryl Hydrocarbon) RN - 0 (Transcription Factors) RN - 138391-32-9 (Aryl Hydrocarbon Receptor Nuclear Translocator) RN - 3XMK78S47O (Testosterone) SB - IM MH - Animals MH - Aryl Hydrocarbon Receptor Nuclear Translocator MH - DNA-Binding Proteins/*metabolism MH - Epididymis/blood supply/*metabolism MH - Hypoxia-Inducible Factor 1, alpha Subunit MH - Immunoblotting MH - Immunohistochemistry MH - Ischemia/metabolism MH - Male MH - Orchiectomy MH - RNA, Messenger/metabolism MH - Rats MH - Rats, Sprague-Dawley MH - Receptors, Aryl Hydrocarbon/*metabolism MH - Spermatozoa/metabolism MH - Testosterone/blood/pharmacology MH - Tissue Distribution MH - Transcription Factors/genetics/*metabolism EDAT- 2003/12/12 05:00 MHDA- 2004/11/04 09:00 CRDT- 2003/12/12 05:00 PHST- 2003/12/12 05:00 [pubmed] PHST- 2004/11/04 09:00 [medline] PHST- 2003/12/12 05:00 [entrez] AID - biolreprod.103.023085 [pii] AID - 10.1095/biolreprod.103.023085 [doi] PST - ppublish SO - Biol Reprod. 2004 Apr;70(4):1121-30. doi: 10.1095/biolreprod.103.023085. Epub 2003 Dec 10.