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骨髓间充质干细胞对重塑小鼠脂多糖诱导的肺损伤的影响。

Impact of bone marrow-derived mesenchymal stem cells on remodeling the lung injury induced by lipopolysaccharides in mice.

作者信息

Mohi El-Din Mouchira M, Rashed Laila A, Mahmoud Haridy Mohi A, Khalil Atef Mohamed, Mohamed Albadry Mohamed A

机构信息

Pathology & Clinical Pathology Department, Faculty of Veterinary Medicine, South Valley University, Qena, Egypt; Pathology & Clinical Pathology Department, Faculty of Veterinary Medicine, South Valley University, Qena, Egypt.

Biochemistry & Molecular Biology Department, Medicine Faculty, Cairo University, Cairo, Egypt; Biochemistry & Molecular Biology Department, Medicine Faculty, Cairo University, Cairo, Egypt.

出版信息

Future Sci OA. 2017 Jan 17;3(1):FSO162. doi: 10.4155/fsoa-2016-0036. eCollection 2017 Mar.

DOI:10.4155/fsoa-2016-0036
PMID:28344826
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5351512/
Abstract

AIM

This study evaluated the potential of bone marrow derived mesenchymal stem cells (MSCs) to regulate cytokines and remodel the lung induced by lipopolysaccharide (LPS; O-antigen).

MATERIALS & METHODS: A group of mice (n = 21) was inoculated intraperitoneally with one dose 0.1 ml containing 0.025 mg LPS/mouse, and another treated intravenously with one dose of labeling bone marrow derived MSCs at 7.5 × 10 cell/mouse 4 h after LPS injection. All animals were sacrificed on the 1st, 7th and 14th days post-injection.

RESULTS

MSCs increased the level of IL-10 with suppression of TNF-α, decrease of collagen fibers and renewal of alveolar type I cells, together with lung tissue remodeling.

CONCLUSION

MSCs were shown to modulate inflammatory cytokines (TNF-α and IL-10) and to differentiate into alveolar type I cells, which prevented fibrosis in lung tissue from LPS-treated mice.

摘要

目的

本研究评估了骨髓间充质干细胞(MSCs)调节细胞因子以及重塑脂多糖(LPS;O抗原)诱导的肺组织的潜力。

材料与方法

一组小鼠(n = 21)腹腔注射一剂0.1 ml含0.025 mg LPS/小鼠,另一组在LPS注射后4小时静脉注射一剂标记的骨髓间充质干细胞,剂量为7.5×10⁶细胞/小鼠。所有动物在注射后第1、7和14天处死。

结果

间充质干细胞增加了IL-10水平,抑制了TNF-α,减少了胶原纤维并使I型肺泡细胞更新,同时伴有肺组织重塑。

结论

间充质干细胞被证明可调节炎性细胞因子(TNF-α和IL-10)并分化为I型肺泡细胞,从而预防LPS处理小鼠的肺组织纤维化。

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