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神经元神经节苷脂和糖鞘脂(GSL)代谢与疾病:继发性代谢错误级联可导致复杂的病理(在 LSDs 中)。

Neuronal Ganglioside and Glycosphingolipid (GSL) Metabolism and Disease : Cascades of Secondary Metabolic Errors Can Generate Complex Pathologies (in LSDs).

机构信息

Lipid Pathobiochemistry Group, German Cancer Research Center, Heidelberg, Germany.

LIMES, c/o Kekule-Institute for Organic Chemistry and Biochemistry, University of Bonn, Bonn, Germany.

出版信息

Adv Neurobiol. 2023;29:333-390. doi: 10.1007/978-3-031-12390-0_12.

Abstract

Glycosphingolipids (GSLs) are a diverse group of membrane components occurring mainly on the surfaces of mammalian cells. They and their metabolites have a role in intercellular communication, serving as versatile biochemical signals (Kaltner et al, Biochem J 476(18):2623-2655, 2019) and in many cellular pathways. Anionic GSLs, the sialic acid containing gangliosides (GGs), are essential constituents of neuronal cell surfaces, whereas anionic sulfatides are key components of myelin and myelin forming oligodendrocytes. The stepwise biosynthetic pathways of GSLs occur at and lead along the membranes of organellar surfaces of the secretory pathway. After formation of the hydrophobic ceramide membrane anchor of GSLs at the ER, membrane-spanning glycosyltransferases (GTs) of the Golgi and Trans-Golgi network generate cell type-specific GSL patterns for cellular surfaces. GSLs of the cellular plasma membrane can reach intra-lysosomal, i.e. luminal, vesicles (ILVs) by endocytic pathways for degradation. Soluble glycoproteins, the glycosidases, lipid binding and transfer proteins and acid ceramidase are needed for the lysosomal catabolism of GSLs at ILV-membrane surfaces. Inherited mutations triggering a functional loss of glycosylated lysosomal hydrolases and lipid binding proteins involved in GSL degradation cause a primary lysosomal accumulation of their non-degradable GSL substrates in lysosomal storage diseases (LSDs). Lipid binding proteins, the SAPs, and the various lipids of the ILV-membranes regulate GSL catabolism, but also primary storage compounds such as sphingomyelin (SM), cholesterol (Chol.), or chondroitin sulfate can effectively inhibit catabolic lysosomal pathways of GSLs. This causes cascades of metabolic errors, accumulating secondary lysosomal GSL- and GG- storage that can trigger a complex pathology (Breiden and Sandhoff, Int J Mol Sci 21(7):2566, 2020).

摘要

糖脂(GSLs)是一组主要存在于哺乳动物细胞表面的膜成分,具有多样性。它们及其代谢产物在细胞间通讯中发挥作用,作为多功能生化信号(Kaltner 等人,Biochem J 476(18):2623-2655, 2019)和许多细胞途径中发挥作用。阴离子糖脂,即含有唾液酸的神经节苷脂(GGs),是神经元细胞表面的重要组成部分,而阴离子硫酸脑苷脂是髓鞘和形成髓鞘的少突胶质细胞的关键成分。GSL 的逐步生物合成途径发生在分泌途径的细胞器表面的膜上,并沿着这些膜进行。在 ER 上形成 GSL 的疏水性神经酰胺膜锚定物之后,高尔基体和反高尔基网络中的跨膜糖基转移酶(GTs)为细胞表面生成细胞类型特异性的 GSL 模式。质膜上的 GSL 可以通过内吞途径到达溶酶体内部,即腔室(ILVs),进行降解。溶酶体中 GSL 代谢需要溶酶体腔内囊泡(ILV)膜表面的可溶性糖蛋白、糖苷酶、脂质结合和转运蛋白以及酸性神经酰胺酶。引起糖基化溶酶体水解酶功能丧失的遗传突变以及参与 GSL 降解的脂质结合蛋白会导致其不可降解的 GSL 底物在溶酶体贮积病(LSD)中在溶酶体中积累。脂质结合蛋白、SAPs 以及 ILV 膜中的各种脂质调节 GSL 代谢,但也像鞘磷脂(SM)、胆固醇(Chol.)或硫酸软骨素等初级贮存化合物可以有效地抑制 GSL 的溶酶体代谢途径。这会引发代谢错误的级联反应,积累次级溶酶体 GSL 和 GG 贮存,从而引发复杂的病理(Breiden 和 Sandhoff,Int J Mol Sci 21(7):2566, 2020)。

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