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BOR - Papers in Press, published online ahead of print October 1, 2003.
Biol Reprod 2003, 10.1095/biolreprod.103.021329
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BIOLOGY OF REPRODUCTION 70, 267–276 (2004)
DOI: 10.1095/biolreprod.103.021329
© 2004 by the Society for the Study of Reproduction, Inc.


Minireview

Nitric Oxide/Nitric Oxide Synthase, Spermatogenesis, and Tight Junction Dynamics1

Nikki P.Y. Lee, and C. Yan Cheng2

Population Council, 1230 York Avenue, New York, New York 10021

During spermatogenesis, preleptotene and leptotene spermatocytes, residing in the basal compartment of the seminiferous epithelium, must traverse the blood-testis barrier (BTB) to gain entry to the adluminal compartment for further development at late stage VIII and early stage IX of the epithelial cycle. As such, the timely opening and closing of the BTB is crucial to spermatogenesis. A compromise in this process can lead to infertility. Moreover, the BTB is unique in its relative localization in the seminiferous epithelium compared to the tight junctions (TJs) found in other epithelia. Sertoli cell TJs are situated near the basal lamina in the testis, closest to the basement membrane (a modified form of extracellular matrix [ECM]), unlike TJs found in other epithelia, which are found nearest the apical portion of an epithelium, farthest away from ECM. Needless to say, BTB function in the testis is maintained by intricate regulatory mechanisms. In addition to hormones and cytokines, nitric oxide (NO) was recently shown to be a putative TJ regulator in the testis. Perhaps equally important, TJ dynamics in the testis were shown to be regulated, at least in part, by occludin, a TJ-integral membrane protein, via the NO/soluble guanylate cyclase/cGMP/protein kinase G signaling pathway. This minireview summarizes recent advances in the field regarding the role of NO in testicular function, with special emphasis regarding its role in TJ dynamics and the likely implications of these studies for male contraceptive development.

1 Supported in part by grants from the CONRAD Program (CICCR CIG-96-05B, CIG-01-72 to C.Y.C.), National Institutes of Health (NICHD, UOI HD45908 to C.Y.C.; U54 HD29990, Project 3 to C.Y.C.; U54 HD13541-20S to C.Y.C.) and the Noopolis Foundation. N.P.Y.L. was supported in part by a Hong Kong University Research Scholarship Award.

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




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