Characterization of Konjac Ceramide (kCer) Binding to Sema3A Receptor Nrpl

被引:4
|
作者
Usuki, Seigo [1 ]
Tamura, Noriko [2 ]
Tamura, Tomohiro [2 ]
Mukai, Katsuyuki [3 ]
Igarashi, Yasuyuki [1 ]
机构
[1] Hokkaido Univ, Fac Adv Life Sci, Lipid Biofunct Sect, Frontier Res Ctr Adv Mat & Life Sci, Sapporo, Hokkaido, Japan
[2] Natl Inst Adv Ind Sci & Technol, Sapporo, Hokkaido, Japan
[3] Daicel Corp, R&D Headquarters, Tokyo, Japan
关键词
ceramide; konjac; NGF; semaphorin; 3A; neurite outgrowth; CRMP2; SEMAPHORIN-3A; EXPRESSION; ITCH;
D O I
10.5650/jos.ess17142
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Konjac ceramide (kCer) can be prepared by a chemoenzymatic method as previously published (Usuki, S.; Tamura, N.; Sakai, S.; Tamura, T.; Mukai, K.; Igarashi, Y. Biochem. Biophys. Rep. 5, 160-167 (2016)). Thus prepared kCer showed an activation effect on Sema3A signaling pathway to induce phosphorylation of CRMP2 and microtubule depolymerizaion, resulting in opposing NGF-induced neurite outgrowth. In the present study, we have shown that kCer is a potential Sema3A-like ligand that has a competitive effect on Sema3A binding to a cell surface receptor Nrpl, but animal-type ceramides have no effect on Sema3A binding to Nrpl. In addition, kCer showed a direct molecular interaction with Nrpl, but animal-type ceramides, Cl6Cer, Cl8Cer, and C24Cer show no specific bindings to Nrpl. Further, kCer showed an additive effect to activate the Sema3A signaling pathway together with low-dose Sema3A but a reversed effect to inhibit this pathway when combined with high-dose Sema3A.
引用
收藏
页码:87 / 94
页数:8
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