Endothelial cell activation and neovascularization are prominent in dermatomyositis.

Kanneboyina Nagaraju, Lisa G Rider, Chenguang Fan, Yi-Wen Chen, Megan Mitsak, Rashmi Rawat, Kathleen Patterson, Cecilia Grundtman, Frederick W Miller, Paul H Plotz, Eric Hoffman, Ingrid E Lundberg
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引用次数: 71

Abstract

Background: While vascular and immune abnormalities are common in juvenile and adult dermatomyositis (DM), the molecular changes that contribute to these abnormalities are not clear. Therefore, we investigated pathways that facilitate new blood vessel formation and dendritic cell migration in dermatomyositis.

Methods: Muscle biopsies from subjects with DM (9 children and 6 adults) and non-myositis controls (6 children and 7 adults) were investigated by immunohistochemistry using antibodies that recognize existing (anti-CD146) and newly formed blood vessels (anti-alphaVbeta3) and mature dendritic cells (anti-DC-LAMP). Blood vessel quantification was performed by digitalized image analysis. Additional muscle biopsies from subjects with adult DM and non-myositis controls were used for global gene expression profiling experiments.

Results: A significant increase in neovascularization was found in muscle biopsies of DM patients; neovascularization (alphaVbeta3 positive capillaries and vessels per muscle fiber) was much higher in juvenile than in adult DM patients (control vs juvenile DM: Mean +/- SE: 0.06 +/- 0.01 vs 0.6 +/- 0.05; p < 0.0001 and control vs adult DM: Mean +/- SE: 0.60 +/- 0.1 vs 0.75 +/- 0.1; p = 0.051). Gene expression analysis demonstrated that genes that participate not only in angiogenesis but also in leukocyte trafficking and the complement cascade were highly up regulated in DM muscle in comparison to age matched controls. DC-LAMP positive dendritic cells were highly enriched at perivascular inflammatory sites in juvenile and adult DM patients along with molecules that facilitate dendritic cell transmigration and reverse transmigration (CD142 and CD31).

Conclusion: These results suggest active neovascularization and endothelial cell activation in both juvenile and adult DM. It is likely that close association of monocytes with endothelial cells initiate rapid dendritic cell maturation and an autoimmune response in DM.

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内皮细胞活化和新生血管在皮肌炎中表现突出。
背景:虽然血管和免疫异常在青少年和成人皮肌炎(DM)中很常见,但导致这些异常的分子变化尚不清楚。因此,我们研究了皮肌炎中促进新血管形成和树突状细胞迁移的途径。方法:采用免疫组化方法对DM患者(9名儿童和6名成人)和非肌炎对照组(6名儿童和7名成人)的肌肉活检进行研究,使用识别现有(抗cd146)和新形成的血管(抗alphavbeta3)和成熟树突状细胞(抗dc - lamp)的抗体。通过数字化图像分析进行血管定量。来自成人糖尿病患者和非肌炎对照组的额外肌肉活检用于全球基因表达谱实验。结果:DM患者肌肉活检中新生血管明显增多;青少年糖尿病患者的新生血管(alphaVbeta3阳性毛细血管和每条肌纤维的血管)远高于成年糖尿病患者(对照组与青少年糖尿病:平均+/- SE: 0.06 +/- 0.01 vs 0.6 +/- 0.05;p < 0.0001,对照组与成人DM:平均+/- SE: 0.60 +/- 0.1 vs 0.75 +/- 0.1;P = 0.051)。基因表达分析表明,与年龄匹配的对照组相比,糖尿病肌肉中不仅参与血管生成,还参与白细胞运输和补体级联的基因被高度上调。DC-LAMP阳性树突状细胞在青少年和成人糖尿病患者的血管周围炎症部位高度富集,并伴有促进树突状细胞迁移和逆转迁移的分子(CD142和CD31)。结论:这些结果表明,在青少年和成人糖尿病中,活跃的新生血管和内皮细胞激活。单核细胞与内皮细胞的密切联系可能启动了糖尿病中快速的树突状细胞成熟和自身免疫反应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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