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Implications of caveolae in testicular and epididymal myoid cells to sperm motility

Oliveira, Regiana L.; Parent, Adam; Cyr, Daniel G.; Gregory, Mary; Mandato, Craig A.; Smith, Chalres E.; Hermo, Louis (2016). Implications of caveolae in testicular and epididymal myoid cells to sperm motility Molecular Reproduction and Development , vol. 83 . p. 526-540. DOI: 10.1002/mrd.22649.

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Résumé

Seminiferous tubules of the testis and epididymal tubules in adult rodents are enveloped by contractile myoid cells, which move sperm and fluids along the male reproductive tract. Myoid cells in the testis influence Sertoli cells by paracrine signaling, but their role in the epididymis is unknown. Electron microscopy revealed that elongated myoid cells formed several concentric layers arranged in a loose configuration. The edges of some myoid cells in a given layer closely approximated one another, and extended small foot-like processes to cells of overlying layers. Gap junction proteins, connexins 32 and 43, were detected within the myoid cell layers by immunohistochemistry. These myoid cells also contained caveolae that contained caveolin-1 and cavin-1 (also known as PTRF). The number of caveolae per unit area of plasma membrane was significantly reduced in caveolin-1-deficient mice (Cav1-/- ). Morphometric analyses of Cav1-null testes revealed an enlargement in whole-tubule and epithelial profile areas, whereas these parameters were slightly reduced in the epididymis. Although sperm are non-motile as they pass through the proximal epididymis, statistical analyses of cauda epididymidis sperm concentrations revealed no significant differences between wild-type and Cav1-/- mice. Motility analyses, however, indicated that sperm velocity parameters were reduced while beat cross frequency was higher in gametes of Cav1-/- mice. Thus while caveolae and their associated proteins are not necessary for myoid cell contractility, they appear to be crucial for signaling with the epididymal epithelium to regulate the proper acquisition of sperm motility.

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Centre: Centre INRS-Institut Armand Frappier
Date de dépôt: 29 mai 2017 19:33
Dernière modification: 29 mai 2017 19:33
URI: http://espace.inrs.ca/id/eprint/4580

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