• 中国科学论文统计源期刊
  • 中国科技核心期刊
  • 美国化学文摘(CA)来源期刊
  • 日本科学技术振兴机构数据库(JST)

临床输血与检验 ›› 2022, Vol. 24 ›› Issue (6): 693-697.DOI: 10.3969/j.issn.1671-2587.2022.06.003

• 基础研究 • 上一篇    下一篇

骨相关间充质干细胞CD166+亚群治疗炎性肠病模型小鼠的研究*

孟炜程, 陈要臻, 安宁, 张婧, 陈禹彤, 胡兴斌   

  1. 710032 空军军医大学第一附属医院输血科
  • 收稿日期:2022-09-06 发布日期:2023-01-05
  • 通讯作者: 胡兴斌,男,副教授,主要从事输血医学研究,(E-mail)hxbyqh@163.com。
  • 作者简介:孟炜程(1998-),男,硕士,主要从事临床检验诊断学研究,(E-mail)mf1151483515@163.com。
  • 基金资助:
    *本课题受国家自然科学基金青年项目(No.31801146),陕西省社发攻关重点研发计划(No.2018SF-199)资助

CD166+ Subpopulation of Bone-Associated Mesenchymal Stem Cells in the Treatment of Inflammatory Bowel Disease in mouse Models

MENG Wei-cheng, CHEN Yao-zhen, AN Ning, et al   

  1. Department of Blood Transfusion, Xijing Hospital, Air Force Military Medical University, Xi'an 710032
  • Received:2022-09-06 Published:2023-01-05

摘要: 目的 初步探讨骨相关间充质干细胞CD166+亚群应用于炎症性肠病(IBD)的治疗效果。方法 将野生C57BL/6小鼠的股骨和胫骨剔除肌肉再去除骨髓细胞后,胶原酶消化获得骨相关间充质干细胞后,使用间充质干细胞富集试剂盒和CD166阳性磁珠分选试剂盒分选得到CD166+MSCs。使用3%葡聚糖硫酸钠(DSS)诱导IBD小鼠模型,将造模成功的小鼠平均分为CD166+MSCs处理组和对照组,CD166+MSCs处理组小鼠给予静脉输注CD166+MSCs,对照组给予PBS,每日观察小鼠的血便情况和记录体重,输注3 d后检测各组小鼠结肠长度,并做病理切片组织染色分析,观察结肠组织病理改变。结果 与对照组相比,CD166+MSCs处理组便血程度明显减轻,结肠长度明显增加,组织病理学切片中的隐窝破坏较少,杯状细胞增多,组织病理学评分较低。结论 对于IBD疾病模型移植CD166+MSCs可获得较显著的治疗效果。

关键词: 炎症性肠病, 骨相关间充质干细胞, CD166

Abstract: Objective To investigate the therapeutic effect of the CD166+subpopulation of bone-associated mesenchymal stem cells applied in inflammatory bowel disease (IBD). Methods After removing bone marrow cells from the femur and tibia of C57/BL6 mice, we performed collagenase digestion to obtain bone-associated cells, and sorted CD166+MSCs using an MSC enrichment kit and a CD166-positive magnetic bead sorting kit. A mouse model of IBD was induced using 3% dextran sodium sulfate (DSS), and the successfully molded mice were equally divided into the CD166+MSCs-treated and control groups. Mice in the CD166+MSCs-treated group were given an intravenous infusion of CD166+MSCs, while the control group was given PBS. The mice were observed daily for bloody stool, and body weight was recorded. After three days of infusion, the colon length of mice in each group was examined, and pathological tissue slices were stained and analyzed to observe the histopathological changes in the colon. Results Compared with the control group, the CD166+MSCs-treated group showed significantly less blood in the stool, significantly longer colon length, less destruction of the crypt in pathological tissue slice, more goblet cells, and lower histopathological score. Conclusion Transplantation of CD166+MSCs in the IBD disease model resulted in a better therapeutic effect.

Key words: Inflammatory bowel disease, Bone-associated mesenchymal stem cells, CD166

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