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Fas与Fas配体的相互作用在炎性肌病中诱导细胞凋亡:在多发性肌炎中,CD4 + T细胞直接导致肌肉细胞损伤。

Fas and Fas ligand interaction induces apoptosis in inflammatory myopathies: CD4+ T cells cause muscle cell injury directly in polymyositis.

作者信息

Sugiura T, Murakawa Y, Nagai A, Kondo M, Kobayashi S

机构信息

Shimane Medical University, Izumo, Japan.

出版信息

Arthritis Rheum. 1999 Feb;42(2):291-8. doi: 10.1002/1529-0131(199902)42:2<291::AID-ANR11>3.0.CO;2-1.

Abstract

OBJECTIVE

To investigate the involvement of the Fas/Fas ligand (Fas/FasL) system in the inflammatory myopathies.

METHODS

Frozen muscle sections obtained from 7 patients with polymyositis (PM), 4 patients with dermatomyositis (DM), and 3 controls were studied by immunochemistry. Apoptosis was detected by DNA electrophoresis and in situ labeling using the TUNEL method.

RESULTS

Fas was detected on muscle fibers and infiltrating mononuclear cells (MNC) in 6 PM patients and 2 DM patients. FasL was expressed mainly on CD4+ T cells and some CD8+ T cells, and on macrophages surrounding Fas-positive muscles in 4 PM patients and 1 DM patient. In 3 of the 5 patients with FasL-positive MNC, the TUNEL method showed that both invaded myonuclei and MNC underwent apoptosis. Chromosomal DNA from the muscle tissue of these patients showed ladder formation.

CONCLUSION

Fas/FasL is involved in muscle cell apoptosis in at least 2 of the inflammatory myopathies, PM and DM. Although CD8+-mediated cytotoxicity is thought to be the main mechanism of muscle injury in PM, our data suggest that CD4+ T cells also directly cause muscle cell damage.

摘要

目的

研究Fas/Fas配体(Fas/FasL)系统在炎性肌病中的作用。

方法

采用免疫化学方法对7例多发性肌炎(PM)患者、4例皮肌炎(DM)患者和3例对照者的冰冻肌肉切片进行研究。通过DNA电泳和TUNEL原位标记法检测细胞凋亡。

结果

在6例PM患者和2例DM患者的肌纤维和浸润的单核细胞(MNC)上检测到Fas。FasL主要表达于4例PM患者和1例DM患者的CD4⁺T细胞及部分CD8⁺T细胞,以及Fas阳性肌肉周围的巨噬细胞上。在5例FasL阳性MNC患者中的3例,TUNEL法显示侵入的肌核和MNC均发生凋亡。这些患者肌肉组织的染色体DNA呈梯状条带形成。

结论

Fas/FasL至少参与了炎性肌病中PM和DM的2种肌肉细胞凋亡。虽然CD8⁺介导的细胞毒性被认为是PM中肌肉损伤的主要机制,但我们的数据表明CD4⁺T细胞也直接导致肌肉细胞损伤。

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