Publication: Accumulation of seminolipid in sertoli cells is associated with increased levels of reactive oxygen species and male subfertility: Studies in aging arsa null male mice
Issued Date
2021-06-01
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ISSN
20763921
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2-s2.0-85107175671
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Mahidol University
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SCOPUS
Bibliographic Citation
Antioxidants. Vol.10, No.6 (2021)
Suggested Citation
Kessiri Kongmanas, Arpornrad Saewu, Wongsakorn Kiattiburut, Mark A. Baker, Kym F. Faull, Dylan Burger, Nongnuj Tanphaichitr Accumulation of seminolipid in sertoli cells is associated with increased levels of reactive oxygen species and male subfertility: Studies in aging arsa null male mice. Antioxidants. Vol.10, No.6 (2021). doi:10.3390/antiox10060912 Retrieved from: https://repository.li.mahidol.ac.th/handle/20.500.14594/76161
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Title
Accumulation of seminolipid in sertoli cells is associated with increased levels of reactive oxygen species and male subfertility: Studies in aging arsa null male mice
Abstract
Seminolipid (also known as sulfogalactosylglycerolipid-SGG), present selectively in male germ cells, plays important roles in spermatogenesis and sperm–egg interaction. The proper degradation of SGG in apoptotic germ cells is also as important. Sertoli cells first phagocytose apoptotic germ cells, then Sertoli lysosomal arylsulfatase A (ARSA) desulfates SGG, the first step of SGG degradation. We have reported that aging male Arsa−/− mice become subfertile with SGG accumulation in Sertoli cell lysosomes, typical of a lysosomal storage disorder (LSD). Since reactive oxygen species (ROS) levels are increased in other glycolipid-accumulated LSDs, we quantified ROS in Arsa−/− Sertoli cells. Our analyses indicated increases in superoxide and H2O2 in Arsa−/− Sertoli cells with elevated apoptosis rates, relative to WT counterparts. Excess H2O2 from Arsa−/− Sertoli cells could travel into testicular germ cells (TGCs) to induce ROS production. Our results indeed indicated higher superoxide levels in Arsa−/− TGCs, compared with WT TGCs. Increased ROS levels in Arsa−/− Sertoli cells and TGCs likely caused the decrease in spermatogenesis and increased the abnormal sperm population in aging Arsa−/− mice, including the 50% decrease in sperm SGG with egg binding ability. In summary, our study indicated that increased ROS production was the mechanism through which subfertility manifested following SGG accumulation in Sertoli cells.