Institute of Protein Biochemistry, National Research Council, Via P. Castellino 111, Napoli, Italy
Institute of Protein Biochemistry, National Research Council, Via P. Castellino 111, Napoli, Italy.
J Cell Sci. 2018 Dec 17;131(24):jcs219204. doi: 10.1242/jcs.219204.
Glycosphingolipids (GSLs) are ubiquitous components of eukaryotic plasma membranes that consist of a ceramide backbone linked to a glycan moiety. Both the ceramide and the glycan parts of GSLs display structural variations that result in a remarkable repertoire of diverse compounds. This diversity of GSLs is exploited during embryogenesis, when different GSLs are produced at specific developmental stages and along several differentiation trajectories. Importantly, plasma membrane receptors interact with GSLs to modify their activities. Consequently, two otherwise identical cells can respond differently to the same stimulus owing to their different GSL composition. The metabolic reprograming of GSLs is in fact a necessary part of developmental programs, as its impairment results in developmental failure or tissue-specific defects. Moreover, single-cell variability is emerging as a fundamental player in development: GSL composition displays cell-to-cell variability in syngeneic cell populations owing to the regulatory gene expression circuits involved in microenvironment adaptation and in differentiation. Here, we discuss how GSLs are synthesized and classified and review the role of GSLs in the establishment and maintenance of cell identity. We further highlight the existence of the regulatory circuits that modify GSL pathways and speculate how GSL heterogeneity might contribute to developmental patterning.
糖脂(Glycosphingolipids,GSLs)是真核细胞膜的普遍组成部分,由连接到聚糖部分的神经酰胺骨架组成。GSL 的神经酰胺和聚糖部分都显示出结构变化,导致了多样化的化合物的显著组成。这种 GSL 的多样性在胚胎发生过程中得到了利用,在这个过程中,不同的 GSL 在特定的发育阶段和沿着几个分化轨迹产生。重要的是,质膜受体与 GSL 相互作用以改变它们的活性。因此,由于其不同的 GSL 组成,两个原本相同的细胞可以对相同的刺激产生不同的反应。GSL 的代谢重编程实际上是发育计划的必要组成部分,因为其损伤会导致发育失败或组织特异性缺陷。此外,单细胞变异性正在成为发育的一个基本参与者:由于涉及微环境适应和分化的调节基因表达电路,GSL 组成在同基因细胞群体中表现出细胞间的变异性。在这里,我们讨论了 GSLs 是如何合成和分类的,并回顾了 GSLs 在建立和维持细胞身份中的作用。我们进一步强调了修饰 GSL 途径的调节电路的存在,并推测了 GSL 异质性如何有助于发育模式。