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内皮细胞活化和新血管形成在皮肌炎中较为突出。

Endothelial cell activation and neovascularization are prominent in dermatomyositis.

作者信息

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

机构信息

Children's National Medical Center, Research Center for Genetic Medicine, 111 Michigan Ave NW, Washington, DC 20010, USA.

出版信息

J Autoimmune Dis. 2006 Feb 20;3:2. doi: 10.1186/1740-2557-3-2.

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.

摘要

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,我们研究了促进皮肌炎中新生血管形成和树突状细胞迁移的途径。

方法

通过免疫组织化学,使用识别现有血管(抗CD146)、新形成血管(抗αVβ3)和成熟树突状细胞(抗DC-LAMP)的抗体,对DM患者(9名儿童和6名成人)和非肌炎对照者(6名儿童和7名成人)的肌肉活检标本进行研究。通过数字化图像分析进行血管定量。来自成年DM患者和非肌炎对照者的额外肌肉活检标本用于全基因组表达谱实验。

结果

在DM患者的肌肉活检标本中发现新生血管形成显著增加;青少年DM患者的新生血管形成(每根肌纤维中αVβ3阳性毛细血管和血管)比成年DM患者高得多(对照组与青少年DM:平均值±标准误:0.06±0.01对0.6±0.05;p<0.0001,对照组与成年DM:平均值±标准误:0.60±0.1对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,不仅参与血管生成,而且参与白细胞运输和补体级联反应的基因在DM肌肉中高度上调。DC-LAMP阳性树突状细胞在青少年和成年DM患者的血管周围炎症部位高度富集,同时还有促进树突状细胞迁移和反向迁移的分子(CD142和CD31)。

结论

这些结果表明青少年和成年DM中均存在活跃的新生血管形成和内皮细胞活化。单核细胞与内皮细胞的紧密关联可能引发DM中树突状细胞的快速成熟和自身免疫反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d3b/1397829/b1d08a7b7ba6/1740-2557-3-2-1.jpg

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