Document Detail


Coxsackie and adenovirus receptor (CAR) is a product of Sertoli and germ cells in rat testes which is localized at the Sertoli-Sertoli and Sertoli-germ cell interface.
MedLine Citation:
PMID:  17359973     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
The coxsackie and adenovirus receptor (CAR), a putative cell-cell adhesion molecule, has attracted wide interest due to its importance in viral pathogenesis and in mediating adenoviral gene delivery. However, the distribution pattern and physiological function of CAR in the testis is still not clear. Here, we identified CAR in Sertoli cells and germ cells of rats. In vivo studies have shown that CAR resides at the blood-testis barrier as well as at the ectoplasmic specialization. The persistent expression of CAR in rat testes from neonatal period throughout adulthood implicates its role in spermatogenesis. Using primary Sertoli cell cultures, we observed a significant induction of CAR during the formation of Sertoli cell epithelium. Furthermore, CAR was seen to be concentrated at inter-Sertoli cell junctions, co-localizing with tight junction protein marker ZO-1 and adherens junction protein N-cadherin. CAR was also found to be associated with proteins of Src kinase family and its protein level declined after TNFalpha treatment in Sertoli cell cultures. Immunofluorescent staining of isolated germ cells has revealed the presence of CAR on spermatogonia, spermatocytes, round spermatids and elongate spermatids. Taken together, we propose that CAR functions as an adhesion molecule in maintaining the inter-Sertoli cell junctions at the basal compartment of the seminiferous epithelium. In addition, CAR may confer adhesion between Sertoli and germ cells at the Sertoli-germ cell interface. It is possible that the receptor utilized by viral pathogens to breakthrough the epithelial barrier was also employed by developing germ cells to migrate through the inter-Sertoli cell junctions.
Authors:
Claire Q F Wang; Dolores D Mruk; Will M Lee; C Yan Cheng
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Publication Detail:
Type:  Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't     Date:  2007-02-03
Journal Detail:
Title:  Experimental cell research     Volume:  313     ISSN:  0014-4827     ISO Abbreviation:  Exp. Cell Res.     Publication Date:  2007 Apr 
Date Detail:
Created Date:  2007-04-06     Completed Date:  2007-06-05     Revised Date:  2013-06-06    
Medline Journal Info:
Nlm Unique ID:  0373226     Medline TA:  Exp Cell Res     Country:  United States    
Other Details:
Languages:  eng     Pagination:  1373-92     Citation Subset:  IM    
Affiliation:
Center for Biomedical Research, The Population Council, 1230 York Avenue, New York, NY 10021, USA.
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MeSH Terms
Descriptor/Qualifier:
Animals
Cell Adhesion Molecules / metabolism
Cell Differentiation
Cells, Cultured
Coxsackie and Adenovirus Receptor-Like Membrane Protein
Germ Cells / metabolism*
Immunoprecipitation
Intercellular Junctions / metabolism*
Junctional Adhesion Molecules
Male
Microfilament Proteins / metabolism
Rats
Rats, Sprague-Dawley
Receptors, Virus / metabolism*
Seminiferous Epithelium / metabolism
Sertoli Cells / drug effects,  metabolism*
Testis / cytology,  growth & development,  metabolism*
Tumor Necrosis Factor-alpha / pharmacology
Grant Support
ID/Acronym/Agency:
U01 HD045908/HD/NICHD NIH HHS; U01 HD045908/HD/NICHD NIH HHS; U01 HD045908-01/HD/NICHD NIH HHS; U01 HD045908-02/HD/NICHD NIH HHS; U01 HD045908-03/HD/NICHD NIH HHS; U01 HD045908-04/HD/NICHD NIH HHS; U54 HD029990/HD/NICHD NIH HHS; U54 HD029990-110007/HD/NICHD NIH HHS; U54 HD29990/HD/NICHD NIH HHS
Chemical
Reg. No./Substance:
0/Cell Adhesion Molecules; 0/Clmp protein, rat; 0/Coxsackie and Adenovirus Receptor-Like Membrane Protein; 0/Junctional Adhesion Molecules; 0/Microfilament Proteins; 0/Receptors, Virus; 0/Tumor Necrosis Factor-alpha; 0/espin protein, rat
Comments/Corrections

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