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Toll 样受体 2 和 3 激动剂对少突胶质细胞的存活、分化和髓鞘膜形成有不同的影响。

Toll-like receptors 2 and 3 agonists differentially affect oligodendrocyte survival, differentiation, and myelin membrane formation.

机构信息

Delta Crystallon BV, Leiden, The Netherlands.

出版信息

J Neurosci Res. 2012 Feb;90(2):388-98. doi: 10.1002/jnr.22767. Epub 2011 Oct 4.

DOI:10.1002/jnr.22767
PMID:21971760
Abstract

Toll-like receptors (TLRs) play a key role in controlling innate immune responses to a wide variety of pathogen-associated molecules as well as endogenous signals. In addition, TLR expression within nonimmune cells has been recognized as as modulator of cell behavior. In this study we have addressed the question of whether functional TLRs are expressed on oligodendrocytes, the myelinating cells of the central nervous system. Primary cultures of rat oligodendrocytes at different maturation stages were found to express TLR2 and, to lesser extent, TLR3. Immunocytochemical analysis revealed that both TLRs were localized at the cell body and primary processes and were excluded from myelin-like membranes. Interestingly, innate immune receptor ligands were able to modulate oligodendrocyte survival, differentiation, and myelin-like membrane formation, indicating that TLRs on oligodendrocytes are functional. In highly purified oligodendrocytes cultures, the TLR2 agonist zymosan promoted survival, differentiation, and myelin-like membrane formation, whereas poly-I:C, a TLR3 ligand, was a potent inducer of apoptosis. Together, these data indicate that, in addition to other neural cell types, also oligodendrocytes express functional TLRs, which play a role in regulating various aspects of oligodendrocyte behavior.

摘要

Toll 样受体 (TLRs) 在控制对各种病原体相关分子以及内源性信号的先天免疫反应方面发挥着关键作用。此外,人们已经认识到 TLR 在非免疫细胞中的表达是细胞行为的调节剂。在这项研究中,我们探讨了 TLR 是否在少突胶质细胞(中枢神经系统的髓鞘形成细胞)上表达。结果发现,不同成熟阶段的大鼠少突胶质细胞原代培养物表达 TLR2,并且表达程度较低的 TLR3。免疫细胞化学分析显示,这两种 TLR 均定位于细胞体和初级突起,并且被排除在髓鞘样膜之外。有趣的是,先天免疫受体配体能够调节少突胶质细胞的存活、分化和髓鞘样膜形成,表明少突胶质细胞上的 TLR 是有功能的。在高度纯化的少突胶质细胞培养物中,TLR2 激动剂酵母聚糖促进了存活、分化和髓鞘样膜形成,而 TLR3 配体聚肌苷酸:聚胞苷酸是凋亡的有效诱导剂。总之,这些数据表明,除了其他神经细胞类型外,少突胶质细胞也表达功能性 TLR,它们在调节少突胶质细胞行为的各个方面发挥作用。

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