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抑制中性粒细胞介导的组织损伤——间充质干细胞的一项新技能。

Suppression of Neutrophil-Mediated Tissue Damage-A Novel Skill of Mesenchymal Stem Cells.

作者信息

Jiang Dongsheng, Muschhammer Jana, Qi Yu, Kügler Andrea, de Vries Juliane C, Saffarzadeh Mona, Sindrilaru Anca, Beken Seppe Vander, Wlaschek Meinhard, Kluth Mark A, Ganss Christoph, Frank Natasha Y, Frank Markus H, Preissner Klaus T, Scharffetter-Kochanek Karin

机构信息

Department of Dermatology and Allergic Diseases, University of Ulm, Ulm, Germany.

Department of Biochemistry, School of Medicine, Justus-Liebig-University of Giessen, Giessen, Germany.

出版信息

Stem Cells. 2016 Sep;34(9):2393-406. doi: 10.1002/stem.2417. Epub 2016 Jun 27.

DOI:10.1002/stem.2417
PMID:27299700
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5572139/
Abstract

Mesenchymal stem cells (MSCs) are crucial for tissue homeostasis and regeneration. Though of prime interest, their potentially protective role on neutrophil-induced tissue damage, associated with high morbidity and mortality, has not been explored in sufficient detail. Here we report the therapeutic skill of MSCs to suppress unrestrained neutrophil activation and to attenuate severe tissue damage in a murine immune-complex mediated vasculitis model of unbalanced neutrophil activation. MSC-mediated neutrophil suppression was due to intercellular adhesion molecule 1-dependent engulfment of neutrophils by MSCs, decreasing overall neutrophil numbers. Similar to MSCs in their endogenous niche of murine and human vasculitis, therapeutically injected MSCs via upregulation of the extracellular superoxide dismutase (SOD3), reduced superoxide anion concentrations and consequently prevented neutrophil death, neutrophil extracellular trap formation and spillage of matrix degrading neutrophil elastase, gelatinase and myeloperoxidase. SOD3-silenced MSCs did not exert tissue protective effects. Thus, MSCs hold substantial therapeutic promise to counteract tissue damage in conditions with unrestrained neutrophil activation. Stem Cells 2016;34:2393-2406.

摘要

间充质干细胞(MSCs)对于组织稳态和再生至关重要。尽管备受关注,但其对与高发病率和死亡率相关的中性粒细胞诱导的组织损伤的潜在保护作用尚未得到充分研究。在此,我们报告了在中性粒细胞激活失衡的小鼠免疫复合物介导的血管炎模型中,间充质干细胞抑制不受控制的中性粒细胞激活和减轻严重组织损伤的治疗技能。间充质干细胞介导的中性粒细胞抑制是由于间充质干细胞通过细胞间黏附分子1依赖性吞噬中性粒细胞,从而减少了中性粒细胞的总数。与小鼠和人类血管炎内源性微环境中的间充质干细胞类似,经治疗注射的间充质干细胞通过上调细胞外超氧化物歧化酶(SOD3),降低了超氧阴离子浓度,从而防止了中性粒细胞死亡、中性粒细胞胞外陷阱形成以及基质降解性中性粒细胞弹性蛋白酶、明胶酶和髓过氧化物酶的泄漏。沉默SOD3的间充质干细胞不发挥组织保护作用。因此,间充质干细胞在对抗中性粒细胞激活不受控制情况下的组织损伤方面具有巨大的治疗潜力。《干细胞》2016年;34卷:2393 - 2406页

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4702/5572139/5b29065248f8/nihms888780f6.jpg
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