Biol Reprod Email Content Delivery
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


BOR - Papers in Press, published online ahead of print October 12, 2005.
Biol Reprod 2005, 10.1095/biolreprod.105.044735
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
74/2/427    most recent
biolreprod.105.044735v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
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 My Folders
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 Da Silva, N.
Right arrow Articles by Breton, S.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Da Silva, N.
Right arrow Articles by Breton, S.
Agricola
Right arrow Articles by Da Silva, N.
Right arrow Articles by Breton, S.
BIOLOGY OF REPRODUCTION 74, 427–438 (2006)
DOI: 10.1095/biolreprod.105.044735
© 2006 by the Society for the Study of Reproduction, Inc.


Research Article

Postnatal Expression of Aquaporins in Epithelial Cells of the Rat Epididymis1

Nicolas Da Silva 2 , Claudia Silberstein , Valérie Beaulieu , Christine Piétrement , Alfred N. Van Hoek , Dennis Brown , and Sylvie Breton 

Massachusetts General Hospital, Program in Membrane Biology-Nephrology Division, Boston, Massachusetts 02114

ABSTRACT

The mammalian aquaporins (AQPs) are a family of 13 transmembrane channel proteins that are involved in the transport of water in numerous organs. In the male excurrent duct, the movement of fluid and solutes across the epithelium is essential for establishing the proper luminal environment in which sperm mature and are stored. AQP9 is abundantly expressed in the efferent ducts, the epididymis, and the vas deferens, where it could represent an important apical pathway for transmembrane water and solute movement. However, other organs in which water transport is critical, including the kidney, the lung, or the eye, express several different AQPs with a cell-specific pattern. To undertake a systematic analysis of the expression of known AQPs in the postnatal and adult rat epididymis, we examined the expression of their respective mRNAs in epithelial cells isolated by laser capture microdissection (LCM), and we determined their corresponding protein expression pattern by immunofluorescence and Western blotting. Our data show that, whereas AQP9 is the main AQP of the epididymis, the mRNA specific for Aqp2, 5, 7, and 11 are also expressed in epididymal epithelial cells. AQP5 protein colocalizes with AQP9 in the apical membrane of a subpopulation of principal cells in the corpus and cauda regions. Aqp2 mRNA was detected in epithelial cells after the second postnatal week and the amount significantly increased up to adulthood. However, AQP2 protein was detected only in the distal cauda of young rats (between the second and fourth postnatal week). No AQP2 protein was detected in the adult epididymis, indicating that posttranscriptional mechanisms are involved in the regulation of AQP2 expression. In addition, epididymal epithelial cells express significant amounts of the mRNAs coding for AQP7 and 11. No mRNA or protein for AQPs 0, 4, 6, and 8 were detectable in epithelial cells, and Aqp1 was detected in whole epididymal samples, but not in epithelial cells. Thanks to the recent development of microdissection technologies, our observations suggest that epididymal epithelial cells express several members of the AQP family with a region-specific pattern. AQPs may be involved not only in the transepithelial transport of water in the epididymis but also in the postnatal development of this organ, as suggested by the differential expression of AQP2.

epididymis, male reproductive tract


FOOTNOTES

1 Supported by National Institutes of Health Grant DK38452 (to D.B. and S.B.); Cystic Fibrosis Foundation grant BRETON05P0 (to S.B.); and grants from the Committee of American Memorial Hospital of Reims, France, the Conseil Régional de Champagne-Ardenne, France, and the Ministère des Affaires Etrangères (Concours Lavoisier), France (to C.P.). The work performed in the Microscopy Core Facility of the Massachusetts General Hospital Program in Membrane Biology was supported by Center for the Study of Inflammatory Bowel Disease Grant DK43351 and Boston Area Diabetes and Endocrinology Research Center Award DK57521.

2 Correspondence: FAX: 617 643 3182; ndasilva{at}partners.org




This article has been cited by other articles:


Home page
Biol. Reprod.Home page
C.-H. Yeung, C. Callies, A. Rojek, S. Nielsen, and T. G. Cooper
Aquaporin Isoforms Involved in Physiological Volume Regulation of Murine Spermatozoa
Biol Reprod, February 1, 2009; 80(2): 350 - 357.
[Abstract] [Full Text] [PDF]


Home page
Biol. Reprod.Home page
C. Belleannee, N. D. Silva, W.W.C. Shum, M. Marsolais, R. Laprade, D. Brown, and S. Breton
Segmental Expression of the Bradykinin Type 2 Receptor in Rat Efferent Ducts and Epididymis and Its Role in the Regulation of Aquaporin 9
Biol Reprod, January 1, 2009; 80(1): 134 - 143.
[Abstract] [Full Text] [PDF]


Home page
J. Histochem. Cytochem.Home page
L. Hermo, M. Schellenberg, L. Y. Liu, B. Dayanandan, T. Zhang, C. A. Mandato, and C. E. Smith
Membrane Domain Specificity in the Spatial Distribution of Aquaporins 5, 7, 9, and 11 in Efferent Ducts and Epididymis of Rats
J. Histochem. Cytochem., December 1, 2008; 56(12): 1121 - 1135.
[Abstract] [Full Text] [PDF]


Home page
Biol. Reprod.Home page
P. Lybaert, A. M. Vanbellinghen, E. Quertinmont, M. Petein, S. Meuris, and P. Lebrun
KATP Channel Subunits Are Expressed in the Epididymal Epithelium in Several Mammalian Species
Biol Reprod, August 1, 2008; 79(2): 253 - 261.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
C. Pietrement, N. Da Silva, C. Silberstein, M. James, M. Marsolais, A. Van Hoek, D. Brown, N. Pastor-Soler, N. Ameen, R. Laprade, et al.
Role of NHERF1, Cystic Fibrosis Transmembrane Conductance Regulator, and cAMP in the Regulation of Aquaporin 9
J. Biol. Chem., February 1, 2008; 283(5): 2986 - 2996.
[Abstract] [Full Text] [PDF]


Home page
Biol. Reprod.Home page
E. Dube, L. Hermo, P. T.K Chan, and D. G Cyr
Alterations in Gene Expression in the Caput Epididymides of Nonobstructive Azoospermic Men
Biol Reprod, February 1, 2008; 78(2): 342 - 351.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Cell Physiol.Home page
N. Da Silva, W. W. C. Shum, J. El-Annan, T. G. Paunescu, M. McKee, P. J. S. Smith, D. Brown, and S. Breton
Relocalization of the V-ATPase B2 subunit to the apical membrane of epididymal clear cells of mice deficient in the B1 subunit
Am J Physiol Cell Physiol, July 1, 2007; 293(1): C199 - C210.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Cell Physiol.Home page
C. G. Huang, T. Lamitina, P. Agre, and K. Strange
Functional analysis of the aquaporin gene family in Caenorhabditis elegans
Am J Physiol Cell Physiol, May 1, 2007; 292(5): C1867 - C1873.
[Abstract] [Full Text] [PDF]


Home page
Hum Reprod UpdateHome page
H.-F. Huang, R.-H. He, C.-C. Sun, Y. Zhang, Q.-X. Meng, and Y.-Y. Ma
Function of aquaporins in female and male reproductive systems
Hum. Reprod. Update, November 1, 2006; 12(6): 785 - 795.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 2006 by the Society for the Study of Reproduction.