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脊髓损伤的固有免疫反应:星形胶质细胞和小胶质细胞的作用

Resident immune responses to spinal cord injury: role of astrocytes and microglia.

作者信息

Brockie Sydney, Zhou Cindy, Fehlings Michael G

机构信息

Division of Genetics and Development, Krembil Research Institute, University Health Network, Toronto, ON, Canada.

Institute of Medical Science, University of Toronto, Toronto, ON, Canada.

出版信息

Neural Regen Res. 2024 Aug 1;19(8):1678-1685. doi: 10.4103/1673-5374.389630. Epub 2023 Dec 11.

DOI:10.4103/1673-5374.389630
PMID:38103231
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10960308/
Abstract

Spinal cord injury can be traumatic or non-traumatic in origin, with the latter rising in incidence and prevalence with the aging demographics of our society. Moreover, as the global population ages, individuals with co-existent degenerative spinal pathology comprise a growing number of traumatic spinal cord injury cases, especially involving the cervical spinal cord. This makes recovery and treatment approaches particularly challenging as age and comorbidities may limit regenerative capacity. For these reasons, it is critical to better understand the complex milieu of spinal cord injury lesion pathobiology and the ensuing inflammatory response. This review discusses microglia-specific purinergic and cytokine signaling pathways, as well as microglial modulation of synaptic stability and plasticity after injury. Further, we evaluate the role of astrocytes in neurotransmission and calcium signaling, as well as their border-forming response to neural lesions. Both the inflammatory and reparative roles of these cells have eluded our complete understanding and remain key therapeutic targets due to their extensive structural and functional roles in the nervous system. Recent advances have shed light on the roles of glia in neurotransmission and reparative injury responses that will change how interventions are directed. Understanding key processes and existing knowledge gaps will allow future research to effectively target these cells and harness their regenerative potential.

摘要

脊髓损伤的起因可以是创伤性的或非创伤性的,随着我们社会人口老龄化,后者的发病率和患病率正在上升。此外,随着全球人口老龄化,患有退行性脊柱病变的个体在创伤性脊髓损伤病例中所占比例越来越大,尤其是涉及颈脊髓的损伤。由于年龄和合并症可能会限制再生能力,这使得恢复和治疗方法极具挑战性。基于这些原因,更好地了解脊髓损伤病变病理生物学的复杂环境以及随之而来的炎症反应至关重要。本综述讨论了小胶质细胞特异性嘌呤能和细胞因子信号通路,以及损伤后小胶质细胞对突触稳定性和可塑性的调节。此外,我们评估了星形胶质细胞在神经传递和钙信号传导中的作用,以及它们对神经损伤的边界形成反应。这些细胞的炎症和修复作用尚未完全为我们所了解,由于它们在神经系统中广泛的结构和功能作用,仍然是关键的治疗靶点。最近的进展揭示了神经胶质细胞在神经传递和修复性损伤反应中的作用,这将改变干预的方向。了解关键过程和现有的知识空白将使未来的研究能够有效地针对这些细胞并利用它们的再生潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/29a2/10960308/640f24dca4ab/NRR-19-1678-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/29a2/10960308/4c94871d9b3c/NRR-19-1678-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/29a2/10960308/640f24dca4ab/NRR-19-1678-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/29a2/10960308/4c94871d9b3c/NRR-19-1678-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/29a2/10960308/640f24dca4ab/NRR-19-1678-g002.jpg

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