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多发性硬化症:急性病变中天冬氨酸在星形胶质细胞的破坏与再生。

Multiple Sclerosis: Destruction and Regeneration of Astrocytes in Acute Lesions.

机构信息

Department of Medicine, The University of Sydney, Camperdown, NSW, Australia.

出版信息

J Neuropathol Exp Neurol. 2019 Feb 1;78(2):140-156. doi: 10.1093/jnen/nly121.

Abstract

There are reports that astrocyte perivascular endfeet are damaged in some cases of multiple sclerosis (MS). This study was designed to determine the origin and outcome of astrocyte damage in acute, resolving, and inactive plaques. Ten acute plaques from 10 early MS cases and 14 plaques of differing histological age from 9 subacute and chronic cases were examined immunohistochemically. Also examined were nonnecrotic early lesions in 3 patients with neuromyelitis optica (NMO). Plaques from 3 MS cases were examined electron microscopically. The edge zones in each of the 10 acute MS lesions revealed a complete loss of astrocyte cell bodies and their pericapillary, perineuronal, and perivascular foot processes. Dendrophagocytosis of degenerate astrocytes was observed. Astrocyte precursors, similar to those that replace destroyed astrocytes in nonnecrotic NMO lesions, were present in areas depleted of astrocytes. Resolving plaques were repopulated initially by stellate astrocytes that stained negatively for the water channel molecule aquaporin4 (AQP4). In older lesions, astrocytes were predominantly AQP4-positive. Loss and recovery of astrocytes in new MS lesions may be as important as myelin loss as a cause of conduction block responsible for symptoms in patients with relapsing and remitting and secondary progressive MS.

摘要

有报道称,多发性硬化症(MS)的某些病例中星形细胞血管周足会受损。本研究旨在确定急性、缓解和非活跃斑块中星形细胞损伤的起源和结果。对 10 例早期 MS 患者的 10 个急性斑块和 9 例亚急性和慢性病例的 14 个具有不同组织学年龄的斑块进行了免疫组织化学检查。还检查了 3 例视神经脊髓炎(NMO)患者的非坏死性早期病变。对 3 例 MS 患者的斑块进行了电镜检查。在 10 个急性 MS 病变的边缘区,均发现星形细胞体及其围绕毛细血管、神经元周围和血管周足完全缺失。退变星形细胞的树突吞噬现象也观察到了。星形细胞前体细胞,类似于在非坏死性 NMO 病变中替代被破坏的星形细胞的前体细胞,在星形细胞缺失的区域存在。缓解斑块最初由星状星形细胞重新填充,这些细胞对水通道分子 aquaporin4(AQP4)呈阴性染色。在较老的病变中,星形细胞主要是 AQP4 阳性。在新的 MS 病变中,星形细胞的丧失和恢复可能与髓鞘丧失一样重要,是导致复发缓解型和继发进展型 MS 患者症状的传导阻滞的原因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f6a/6330170/bfa0fb243ce1/nly121f1.jpg

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