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Regulation of galectin-3-induced apoptosis of Jurkat cells by both O-glycans and N-glycans on CD45
Authors:Jing Xue  Xiqiang Gao  Chunyan Fu  Zhe CongHong Jiang  Wei WangTing Chen  Qiang Wei  Chuan Qin
Affiliation:Institute of Laboratory Animal Science, Chinese Academy of Medical Sciences (CAMS) and Comparative Medicine Center, Peking Union Medical College (PUMC), Key Laboratory of Human Disease Comparative Medicine, Beijing, China
Abstract:Galectin-3 has been reported to induce apoptosis of Jurkat cells through binding receptors such as CD45. CD45RABC is heavily O-glycosylated and N-glycosylated, while CD45RO is only N-glycosylated. In this study, no apoptosis induced by galectin-3 was detected in CD45RO-transfected cells, whereas apoptosis of CD45RABC-transfected cells was observed, implying that O-glycans on CD45 might play roles in galectin-3-induced apoptosis. O-Glycosylation inhibition assay further suggests the role of O-glycans on CD45 in regulation of galectin-3-induced apoptosis. We also found that deglycosylation at N327 of CD45RO resulted in increased binding to galectin-3 without affecting apoptosis, while deglycosylation at N36 or N109 of CD45RO enhanced galectin-3-induced apoptosis. These data demonstrate that galectin-3-induced apoptosis of Jurkat cells is regulated by both O-glycans and N-glycans on CD45.
Keywords:PBST, phosphate buffered saline with Tween 20   MW, molecular weight   DMEM, Dulbecco&rsquo  s modified Eagle&rsquo  s medium   SDS&ndash  PAGE, sodium dodecyl sulfate&ndash  polyacrylamide gel electrophoresis
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