少突胶质细胞的免疫作用:髓磷脂维持之外。

Discovery immunology Pub Date : 2025-04-28 eCollection Date: 2025-01-01 DOI:10.1093/discim/kyaf005
Juana M Pasquini, Jorge D Correale
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引用次数: 0

摘要

少突胶质细胞(OGDs)是中枢神经系统(CNS)中成熟的细胞,主要因其在髓鞘形成中的作用而被认可。然而,新出现的证据表明,ogd之间的内在差异可能导致不同的功能。ogd的异质性可能取决于其来源、位置、年龄和病理表现。这些变异表明,特定的ogd群体可以调节局部免疫反应,并与其他免疫细胞相互作用,而不仅仅是在髓鞘形成中发挥作用。OGDs表达主要组织相容性复合体I类和II类分子,因此可以分别向CD8 +和CD4 + T细胞呈递内源性和外源性抗原。在生理条件下,ogd释放维持小胶质细胞静止和支持稳态功能的因子。然而,在神经炎症期间,ogd与浸润中枢神经系统的小胶质细胞、星形胶质细胞和外周免疫细胞相互作用,这可能改变它们的信号谱。在炎症条件下,ogd通过产生一系列促炎细胞因子和趋化因子,在中枢神经系统免疫学中发挥积极作用。这些因素对中枢神经系统内免疫细胞迁移和激活的调节至关重要。相反,ogd也可以释放抗炎因子,如脑源性神经营养因子,有助于减轻过度的炎症反应。对ogd如何影响和受邻近细胞影响的研究可能会揭示新的治疗靶点和策略。ogd在免疫学和中枢神经系统功能中的双重作用为促进我们对中枢神经系统疾病的理解和治疗提供了机遇和挑战。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The immunological role of oligodendrocytes: beyond myelin maintenance.

Oligodendrocytes (OGDs) are well-established cells in the central nervous system (CNS), primarily recognized for their role in myelination. However, emerging evidence suggests intrinsic differences among OGDs that may lead to diverse functions. OGDs heterogeneity could depend on their origin, location, age, and the presence of pathology. These variations indicate that specific populations of OGDs can modulate local immune responses and interact with other immune cells beyond their role in myelination. OGDs express major histocompatibility complex class I and class II molecules and can thus present endogenous and exogenous antigens to CD8 + and CD4 + T cells, respectively. In physiological conditions, OGDs release factors that maintain microglial quiescence and support homeostatic functions. However, during neuroinflammation, OGDs interact with microglia, astrocytes, and peripheral immune cells infiltrating the CNS, which may change their signaling profiles. In inflammatory conditions, OGDs demonstrate their active role in CNS immunology by producing a range of pro-inflammatory cytokines and chemokines. These factors are critical to the regulation of immune cell migration and activation within the CNS. Conversely, OGDs can also release anti-inflammatory factors, such as brain-derived neurotrophic factors, which help mitigate excessive inflammatory responses. Research into how OGDs affect and are affected by neighboring cells may unveil new therapeutic targets and strategies. The dual roles of OGDs in immunology and CNS function present both opportunities and challenges for advancing our understanding and treatment of CNS disorders.

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