Male germ cells require polyenoic sphingolipids with complex glycosylation for completion of meiosis -: A link to ceramide synthase-3

被引:96
作者
Rabionet, Mariona [2 ]
van der Spoel, Aarnoud C. [1 ]
Chuang, Chia-Chen [1 ]
von Tuempling-Radosta, Benita [2 ]
Litjens, Manja [1 ]
Bouwmeester, Diane [1 ]
Hellbusch, Christina C. [3 ]
Koerner, Christian [3 ]
Wiegandt, Herbert [1 ,2 ]
Gorgas, Karin [4 ]
Platt, Frances M. [1 ]
Groene, Hermann Josef [2 ]
Sandhoff, Roger [2 ]
机构
[1] Univ Oxford, Dept Pharmacol, Oxford OX1 3QT, England
[2] German Canc Res Ctr, Dept Cellular & Mol Pathol, INF 280, D-69120 Heidelberg, Germany
[3] Univ Childrens Hosp, Div Inborn Metab Dis, Dept Pediat, INF 153, D-69120 Heidelberg, Germany
[4] Heidelberg Univ, Dept Anat & Cell Biol 2, INF 307, D-69120 Heidelberg, Germany
关键词
D O I
10.1074/jbc.M800870200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Previously, it was found that a novel class of neutral fucosylated glycosphingolipids (GSLs) is required for male fertility. These lipids contain very long-chain (C26-C32) polyunsaturated (4-6 double bonds) fatty acid residues (VLC-PUFAs). To assess the role of these complex GSLs in spermatogenesis, we have now investigated with which of the testicular cell types these lipids are associated. During postnatal development, complex glycosylated and simple VLC-PUFA sphingolipids were first detectable at day 15, when the most advanced germ cells are pachytene spermatocytes. Their synthesis is most likely driven by ceramide synthase-3. This enzyme is encoded by the Cers3/Lass3 gene (longevity assurance genes), and out of six members of this gene family, only Cers3 mRNA expression was limited to germ cells, where it was up-regulated more than 700-fold during postnatal testicular maturation. Increasing levels of neutral complex VLC-PUFA GSLs also correlated with the progression of spermatogenesis in a series of male sterile mutants with arrests at different stages of spermatogenesis. Remarkably, fucosylation of the complex VLC-PUFA GSLs was not essential for spermatogenesis, as fucosylation- deficient mice produced nonfucosylated versions of the complex testicular VLC-PUFA GSLs, had complete spermatogenesis, and were fertile. Nevertheless, sterile Galgt1(-/-) mice, with a defective meiotic cytokinesis and a subsequent block in spermiogenesis, lacked complex but contained simple VLC-PUFA GSLs, as well as VLC-PUFA ceramides and sphingomyelins, indicating that the latter lipids are not sufficient for completion of spermatogenesis. Thus, our data imply that both glycans and the particular acyl chains of germinal sphingolipids are relevant for proper completion of meiosis.
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收藏
页码:13357 / 13369
页数:13
相关论文
共 48 条
[21]   Cellular localization of sphingomyelin synthase 2 in the seminiferous epithelium of adult rat testes [J].
Lee, Nikki P. Y. ;
Mruk, Dolores D. ;
Xia, Weiliang ;
Cheng, C. Yan .
JOURNAL OF ENDOCRINOLOGY, 2007, 192 (01) :17-32
[22]   A genetic model of substrate deprivation therapy for a glycosphingolipid storage disorder [J].
Liu, YJ ;
Wada, R ;
Kawai, H ;
Sango, K ;
Deng, CX ;
Tai, T ;
McDonald, MP ;
Araujo, K ;
Crawley, JN ;
Bierfreund, U ;
Sandhoff, K ;
Suzuki, K ;
Proia, RL .
JOURNAL OF CLINICAL INVESTIGATION, 1999, 103 (04) :497-505
[23]   Analysis of relative gene expression data using real-time quantitative PCR and the 2-ΔΔCT method [J].
Livak, KJ ;
Schmittgen, TD .
METHODS, 2001, 25 (04) :402-408
[24]   Mammalian Lass6 and its related family members regulate synthesis of specific ceramides [J].
Mizutani, Y ;
Kihara, A ;
Igarashi, Y .
BIOCHEMICAL JOURNAL, 2005, 390 (01) :263-271
[25]   LASS3 (longevity assurance homologue 3) is a mainly testis-specific (dihydro)ceramide synthase with relatively broad substrate specificity [J].
Mizutani, Yukiko ;
Kihara, Akio ;
Igarashi, Yasuyuki .
BIOCHEMICAL JOURNAL, 2006, 398 (531-538) :531-538
[26]   Sertoli-Sertoli and Sertoli-germ cell interactions and their significance in germ cell movement in the seminiferous epithelium during spermatogenesis [J].
Mruk, DD ;
Cheng, CY .
ENDOCRINE REVIEWS, 2004, 25 (05) :747-806
[27]   Spermiogenesis deficiency and germ-cell apoptosis in CREM-mutant mice [J].
Nantel, F ;
Monaco, L ;
Foulkes, NS ;
Masquilier, D ;
LeMeur, M ;
Henriksen, K ;
Dierich, A ;
Parvinen, M ;
SassoneCorsi, P .
NATURE, 1996, 380 (6570) :159-162
[28]   CALENDAR OF GAMETOGENIC DEVELOPMENT IN PREPUBERAL MALE MOUSE [J].
NEBEL, BR ;
HACKETT, EM ;
AMAROSE, AP .
SCIENCE, 1961, 134 (348) :832-&
[29]   Analysis of fluorescently labeled glycosphingolipid-derived oligosaccharides following ceramide glycanase digestion and anthranilic acid labeling [J].
Neville, DCA ;
Coquard, V ;
Priestman, DA ;
te Vruchte, DJM ;
Sillence, DJ ;
Dwek, RA ;
Platt, FM ;
Butters, TD .
ANALYTICAL BIOCHEMISTRY, 2004, 331 (02) :275-282
[30]   DURATION OF SPERMATOGENESIS IN THE MOUSE AND TIMING OF STAGES OF THE CYCLE OF THE SEMINIFEROUS EPITHELIUM [J].
OAKBERG, EF .
AMERICAN JOURNAL OF ANATOMY, 1956, 99 (03) :507-516