Biol Reprod
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH
 QUICK SEARCH:   [advanced]


     


BOR - Papers in Press, published online ahead of print April 2, 2003.
Biol Reprod 2003, 10.1095/biolreprod.102.011791
This Article
Right arrow Full Text (Rapid PDF)
Right arrow All Versions of this Article:
69/1/310    most recent
biolreprod.102.011791v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Fleming, S. L.
Right arrow Articles by Boekelheide, K.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Fleming, S. L.
Right arrow Articles by Boekelheide, K.
Agricola
Right arrow Articles by Fleming, S. L.
Right arrow Articles by Boekelheide, K.
Submitted September 26, 2002
Returned for revision November 13, 2002
Accepted March 3, 2003

Testis


{gamma}-Tubulin Overexpression in Sertoli Cells In Vivo: I. Localization to Sites of Spermatid Head Attachment and Alterations in Sertoli Cell Microtubule Distribution

Shawna L. Fleming , Peter R. Shank , and Kim Boekelheide *

* To whom correspondence should be addressed. E-mail: kim_boekelheide{at}brown.edu.

Abstract

Sertoli cells play a number of roles in supporting spermatogenesis, including structural organization, physical and paracrine support of germ cells, and secretion of factors necessary for germ cell development. Studies with microtubule disrupting compounds indicate that intact microtubule networks are crucial for normal spermatogenesis. However, treatment with toxicants and pharmacologic agents that target microtubules lack cell-type selectivity, and may therefore elicit direct effects on germ cells, which also require microtubule-mediated activities for division and morphological transformation. To evaluate the importance of Sertoli cell microtubule-based activities for spermatogenesis, an adenoviral vector that overexpresses the microtubule nucleating protein, {gamma}-tubulin, was used to selectively disrupt microtubule networks in Sertoli cells in vivo. {gamma}-Tubulin overexpression was observed to cause redistribution of Sertoli cell microtubule networks, and overexpression of a {gamma}-tubulin-EGFP fusion protein was observed to localize to the site of elongate spermatid head attachment to the seminiferous epithelium.



Key words: Testis • Toxicology • Sertoli cells • Spermatogenesis



This article has been cited by other articles:


Home page
Toxicol SciHome page
R. J. Markelewicz Jr., S. J. Hall, and K. Boekelheide
2,5-Hexanedione and Carbendazim Coexposure Synergistically Disrupts Rat Spermatogenesis Despite Opposing Molecular Effects on Microtubules
Toxicol. Sci., July 1, 2004; 80(1): 92 - 100.
[Abstract] [Full Text] [PDF]


Home page
Hum Reprod UpdateHome page
N. P.Y. Lee and C. Y. Cheng
Ectoplasmic specialization, a testis-specific cell-cell actin-based adherens junction type: is this a potential target for male contraceptive development?
Hum. Reprod. Update, July 1, 2004; 10(4): 349 - 369.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH
Copyright © 2003 by the Society for the Study of Reproduction.