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Properties, metabolism and roles of sulfogalactosylglycerolipid in male reproduction.

Authors :
Tanphaichitr N
Kongmanas K
Faull KF
Whitelegge J
Compostella F
Goto-Inoue N
Linton JJ
Doyle B
Oko R
Xu H
Panza L
Saewu A
Source :
Progress in lipid research [Prog Lipid Res] 2018 Oct; Vol. 72, pp. 18-41. Date of Electronic Publication: 2018 Aug 25.
Publication Year :
2018

Abstract

Sulfogalactosylglycerolipid (SGG, aka seminolipid) is selectively synthesized in high amounts in mammalian testicular germ cells (TGCs). SGG is an ordered lipid and directly involved in cell adhesion. SGG is indispensable for spermatogenesis, a process that greatly depends on interaction between Sertoli cells and TGCs. Spermatogenesis is disrupted in mice null for Cgt and Cst, encoding two enzymes essential for SGG biosynthesis. Sperm surface SGG also plays roles in fertilization. All of these results indicate the significance of SGG in male reproduction. SGG homeostasis is also important in male fertility. Approximately 50% of TGCs become apoptotic and phagocytosed by Sertoli cells. SGG in apoptotic remnants needs to be degraded by Sertoli lysosomal enzymes to the lipid backbone. Failure in this event leads to a lysosomal storage disorder and sub-functionality of Sertoli cells, including their support for TGC development, and consequently subfertility. Significantly, both biosynthesis and degradation pathways of the galactosylsulfate head group of SGG are the same as those of sulfogalactosylceramide (SGC), a structurally related sulfoglycolipid important for brain functions. If subfertility in males with gene mutations in SGG/SGC metabolism pathways manifests prior to neurological disorder, sperm SGG levels might be used as a reporting/predicting index of the neurological status.<br /> (Copyright © 2018 Elsevier Ltd. All rights reserved.)

Details

Language :
English
ISSN :
1873-2194
Volume :
72
Database :
MEDLINE
Journal :
Progress in lipid research
Publication Type :
Academic Journal
Accession number :
30149090
Full Text :
https://doi.org/10.1016/j.plipres.2018.08.002