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幼年皮肌炎患者炎症肌肉中的浆细胞样树突状细胞。

Plasmacytoid dendritic cells in inflamed muscle of patients with juvenile dermatomyositis.

作者信息

López de Padilla Consuelo M, Vallejo Abbe N, McNallan Kelly T, Vehe Richard, Smith Stephen A, Dietz Allan B, Vuk-Pavlovic Stanimir, Reed Ann M

机构信息

Mayo Clinic College of Medicine, Rochester, Minnesota, USA.

出版信息

Arthritis Rheum. 2007 May;56(5):1658-68. doi: 10.1002/art.22558.

Abstract

OBJECTIVE

To examine whether dendritic cells (DCs) are constituents of muscle inflammation in juvenile dermatomyositis (DM).

METHODS

The types, numbers, and activation state of DC subsets in inflamed muscle tissue from patients with juvenile DM and in noninflamed muscle tissue from control subjects were examined by multicolor immunofluorescence. Chemokine expression of the muscle-infiltrating cells was examined by laser capture microdissection and quantitative polymerase chain reaction.

RESULTS

Plasmacytoid DCs were the predominant component of the inflamed muscle tissue from patients with juvenile DM. These cells were identified by coexpression of CD4 and CD123, but not CD11c, and also expressed CD83, indicating maturity of the cells. In contrast, in noninflamed muscle, plasmacytoid DCs were scarce and did not express CD83. Mononuclear cells surrounding the blood vessels of inflamed muscle contained abundant transcripts of CCL19 and CCL21, but very little CCL18 transcripts. In contrast, cells from noninflamed muscle contained negligible amounts of CCL19 and CCL21, but had high amounts of CCL18. Both the inflamed and noninflamed muscle tissue had equivalent levels of CXCL12 transcripts, but inflamed muscle contained more transcripts of the CXCL12 receptor CXCR4.

CONCLUSION

These findings are consistent with the idea that plasmacytoid DCs are mediators of muscle inflammation in juvenile DM. The abundance of CD83+ plasmacytoid DCs in perivascular areas and the overexpression of CCL19 and CCL21 in perivascular cellular foci suggest that in situ activation and maturation of resident plasmacytoid DCs are central to the initiation and perpetuation of muscle inflammation in juvenile DM.

摘要

目的

研究树突状细胞(DCs)是否为青少年皮肌炎(DM)肌肉炎症的组成部分。

方法

采用多色免疫荧光法检测青少年DM患者炎症肌肉组织及对照者非炎症肌肉组织中DC亚群的类型、数量和激活状态。通过激光捕获显微切割和定量聚合酶链反应检测肌肉浸润细胞的趋化因子表达。

结果

浆细胞样DCs是青少年DM患者炎症肌肉组织的主要成分。这些细胞通过共表达CD4和CD123而非CD11c来识别,并且还表达CD83,表明细胞成熟。相比之下,在非炎症肌肉中,浆细胞样DCs稀少且不表达CD83。炎症肌肉血管周围的单核细胞含有丰富的CCL19和CCL21转录本,但CCL18转录本很少。相比之下,来自非炎症肌肉的细胞含有可忽略不计的CCL19和CCL21,但CCL18含量很高。炎症和非炎症肌肉组织的CXCL12转录本水平相当,但炎症肌肉含有更多的CXCL12受体CXCR4转录本。

结论

这些发现与浆细胞样DCs是青少年DM肌肉炎症介质的观点一致。血管周围区域CD83 +浆细胞样DCs的丰富以及血管周围细胞灶中CCL19和CCL21的过表达表明,驻留浆细胞样DCs的原位激活和成熟是青少年DM肌肉炎症起始和持续的核心环节。

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