Skip Navigation



Glycobiology Advance Access published online on January 19, 2005

Glycobiology, doi:10.1093/glycob/cwi043
This Article
Right arrow Advance Access manuscript (PDF) Freely available
Right arrow All Versions of this Article:
15/6/649    most recent
cwi043v1
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 Add to My Personal Archive
Right arrow Download to citation manager
Right arrowRequest Permissions
Right arrow Disclaimer
Google Scholar
Right arrow Articles by Zhang, Y.
Right arrow Articles by Honke, K.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Zhang, Y.
Right arrow Articles by Honke, K.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

© Oxford University Press 2004; all rights reserved.
Received December 13, 2004
Revised January 14, 2005
Accepted January 15, 2005

Article

Testis-Specific Sulfoglycolipid, Seminolipid Is Essential for Germ Cell Function in Spermatogenesis

Yanlong Zhang 1, Yoshihiro Hayashi 2, Xinyao Cheng 3, Tae Watanabe 3, Xiangchun Wang 3, Naoyuki Taniguchi 3*, and Koichi Honke 4

1 Department of Molecular Genetics, Kochi University Medical School, Kochi 783-8505,; Department of Biochemistry, Osaka University Medical School, Osaka 565-0871
2 Department of Pathology, Kochi University Medical School, Kochi 783-8505
3 Department of Biochemistry, Osaka University Medical School, Osaka 565-0871
4 Department of Molecular Genetics, Kochi University Medical School, Kochi 783-8505,; CREST, Japan Science and Technology Agency, Japan

* To whom correspondence should be addressed.
Naoyuki Taniguchi, E-mail: proftani{at}biochem.med.osaka-u.ac.jp


   Abstract

More than 90% of the glycolipid in mammalian testis consists of a unique sulfated glyceroglycolipid, seminolipid. The sulfation of the molecule is catalyzed by a Golgi membrane-associated sulfotransferase, cerebroside sulfotransferase (CST). Disruption of the Cst gene in mice results in male infertility due to the arrest of spermatogenesis prior to the metaphase of the first meiosis. However, the issue of which side of the cell function, germ cells or Sertoli cells, is deteriorated in this mutant mouse remains unknown. The findings herein show that that the defect is in the germ cell side, as evidenced by a transplantation analysis, in which wild-type spermatogonia expressing the green fluorescent protein were injected into the seminiferous tubules of CST-null testis. The transplanted green fluorescent protein-positive cells generated colonies and spermatogenesis proceeded over meiosis in the mutant testis. The findings also clearly show that the seminolipid is expressed on the plasma membranes of spermatogonia, spermatocytes, spermatids and spermatozoa , as evidenced by the immunostaining of wild-type testes using an anti-sulfogalactolipid antibody, Sulph-1 in comparison with CST-null testes as a negative control, and that seminolipid appears as early as day 8 of age, when Type B spermatogonia emerge.


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
GlycobiologyHome page
N. Goto-Inoue, T. Hayasaka, N. Zaima, and M. Setou
The specific localization of seminolipid molecular species on mouse testis during testicular maturation revealed by imaging mass spectrometry
Glycobiology, September 1, 2009; 19(9): 950 - 957.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
M. Rabionet, A. C. van der Spoel, C.-C. Chuang, B. von Tumpling-Radosta, M. Litjens, D. Bouwmeester, C. C. Hellbusch, C. Korner, H. Wiegandt, K. Gorgas, et al.
Male Germ Cells Require Polyenoic Sphingolipids with Complex Glycosylation for Completion of Meiosis: A LINK TO CERAMIDE SYNTHASE-3
J. Biol. Chem., May 9, 2008; 283(19): 13357 - 13369.
[Abstract] [Full Text] [PDF]



Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.