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BOR - Papers in Press, published online ahead of print October 31, 2002.
Biol Reprod 2002, 10.1095/biolreprod.102.010371
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BIOLOGY OF REPRODUCTION 68, 1087–1097 (2003)
DOI: 10.1095/biolreprod.102.010371
© 2003 by the Society for the Study of Reproduction, Inc.


Minireview

Sertoli Cell Tight Junction Dynamics: Their Regulation During Spermatogenesis1

Wing-Yee Luia, Dolores Mruka, Will M Leeb, and C. Yan Cheng2,a

a Population Council, Center for Biomedical Research, New York, New York 10021 b Department of Zoology, The University of Hong Kong, Hong Kong, China

During spermatogenesis, developing preleptotene and leptotene spermatocytes must translocate from the basal to the adluminal compartment of the seminiferous epithelium so that fully developed spermatids (spermatozoa) can be released to the tubular lumen at spermiation. It is conceivable that the opening and closing of the inter-Sertoli tight junctions (TJs) that constitute the blood-testis barrier are regulated by an array of intriguingly coordinated signaling pathways and molecules. Several molecules have been shown to regulate Sertoli cell TJ dynamics; they include, for example, transforming growth factor ß3 (TGFß3), occludin, protein kinase A, protein kinase C, and signaling pathways such as the TGFß3/p38 mitogen-activated protein kinase pathway. Yet the mechanisms that regulate these events are essentially not known. This minireview summarizes some of the recent advances in the study of TJ dynamics in the testis and reviews several models that can be used to study TJ dynamics. It also highlights specific areas for future research toward understanding the precise physiological relationship between junction dynamics and spermatogenesis.

1 This work was supported in part by the CONRAD Program (CICCR grants CIG-96-05-A and CIG-01-72 to C.Y.C., and CIG-01-74 to D.M.); by the National Institute for Child Health and Human Development through grant U54 HD-29990, Project 3, to C.Y.C.; by the U.S. Agency for International Development through grant HRN-A-00-99-00010; by the Noopolis Foundation; by the Hong Kong Research Grant Council (HKU 7194/01M to W.M.I. and C.Y.C.). W.Y.L. was supported in part by a postgraduate research scholarship award from the University of Hong Kong.

2 Correspondence: C. Yan Cheng, Population Council, 1230 York Avenue, New York, NY 10021. FAX: 212 327 8733; y-cheng{at}popcbr.rockefeller.edu




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