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脐带间充质干细胞用于抑制次氯酸诱导的系统性硬化症小鼠模型中的纤维化和自身免疫发展

Umbilical Cord Mesenchymal Stem Cells for Inhibiting the Fibrosis and Autoimmune Development in HOCl-Induced Systemic Scleroderma Mouse Model.

作者信息

Jin Xin, Hou Jiali, Zheng Ke, Wei Dan, Zhang Ali, Wang Siqi, Mei Hua, Li Chuang, Cheng Lamei, Sun Xuan

机构信息

Institute of Reproductive and Stem Cell Engineering, School of Basic Medical Sciences, Central South University, Changsha, China.

National Engineering Research Center of Human Stem Cells, Changsha, China.

出版信息

Int J Stem Cells. 2021 Aug 30;14(3):262-274. doi: 10.15283/ijsc20002.

Abstract

BACKGROUND AND OBJECTIVES

Systemic scleroderma (SSc) is a rare and serious connective tissue disease, an autoimmune disease, and a rare refractory disease. In this study, preventive effect of single systemic human umbilical cord mesenchymal stem cells (UC-MSCs) transfusion on SSc was preliminarily explored.

METHODS AND RESULTS

SSc mouse model was established by daily intradermal injection of Hypochlorite (HOCl). SSc mice were treated by single transfusion of UC-MSCs at 0.625×10, 2.5×10 and 1×10 respectively. At the 42nd day of intradermal injection of HOCl, the symptoms showed up by skin and alveolar wall thickening, lymphocytic infiltration, increased collagen in skin/lung, and the increased proportion of CD3CD4CD25FoxP3 cells (a Treg subset) in spleen. After UC-MSCs transfusion, the degree of skin thickening, alveolar wall thickening and lymphocyte infiltration were decreased, the collagen sedimentation in skin/lung was decreased, and the proportion of CD3CD4CD25 FoxP3 cells was decreased.

CONCLUSIONS

UC-MSC can achieve a preventive effect in SSc mice by fibrosis attenuation and immunoregulation.

摘要

背景与目的

系统性硬化症(SSc)是一种罕见且严重的结缔组织疾病、自身免疫性疾病和难治性疾病。本研究初步探讨了单次全身输注人脐带间充质干细胞(UC-MSCs)对系统性硬化症的预防作用。

方法与结果

通过每日皮内注射次氯酸盐(HOCl)建立系统性硬化症小鼠模型。分别以0.625×10、2.5×10和1×10的剂量对系统性硬化症小鼠进行单次UC-MSCs输注治疗。在皮内注射HOCl第42天时,出现皮肤和肺泡壁增厚、淋巴细胞浸润、皮肤/肺中胶原蛋白增加以及脾脏中CD3CD4CD25FoxP3细胞(一种调节性T细胞亚群)比例增加等症状。输注UC-MSCs后,皮肤增厚、肺泡壁增厚和淋巴细胞浸润程度降低,皮肤/肺中胶原蛋白沉积减少,CD3CD4CD25FoxP3细胞比例降低。

结论

UC-MSCs可通过减轻纤维化和免疫调节对系统性硬化症小鼠起到预防作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/efeb/8429945/b848a1663663/ijsc-14-3-262-f1.jpg

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