Hakomori S, Igarashi Y
Biomembrane Institute, Seattle, WA 98119, USA.
J Biochem. 1995 Dec;118(6):1091-103. doi: 10.1093/oxfordjournals.jbchem.a124992.
Glycosphingolipids (GSLs), cell type-specific markers which change dramatically during ontogenesis and oncogenesis, have been implicated as playing major roles in cellular interactions and control of cell proliferation in multicellular organisms. These functional roles have been partially clarified through two types of studies: (i) Studies of cell recognition mediated by (a) GSL-GSL interaction, (b) GSL-lectin interaction, and (c) GSL-dependent modulation of integrin receptor function. (ii) Studies on control of transmembrane signaling by GSLs and/or sphingosine (Sph) derivatives, with emphasis on effects of these compounds on: (a) signaling pathways initiated by tyrosine kinase-linked receptors; (b) signaling systems mediated by protein kinase C, MAP kinase, other kinases, or cytosolic Ca2+ concentration, leading to changes in cellular phenotypes such as motility, proliferation, differentiation, and apoptosis.
糖鞘脂(GSLs)是细胞类型特异性标志物,在个体发育和肿瘤发生过程中会发生显著变化,在多细胞生物的细胞间相互作用和细胞增殖控制中发挥着重要作用。通过两类研究,这些功能作用已得到部分阐明:(i)对由(a)GSL - GSL相互作用、(b)GSL - 凝集素相互作用以及(c)GSL依赖性整合素受体功能调节介导的细胞识别的研究。(ii)对GSLs和/或鞘氨醇(Sph)衍生物对跨膜信号传导控制的研究,重点关注这些化合物对:(a)由酪氨酸激酶连接受体启动的信号通路;(b)由蛋白激酶C、丝裂原活化蛋白激酶、其他激酶或胞质Ca2+浓度介导的信号系统的影响,这些影响会导致细胞表型如运动性、增殖、分化和凋亡的变化。