Kupffer cells-dependent inflammation in the injured liver increases recruitment of mesenchymal stem cells in aging mice

被引:19
|
作者
Yang, Xue [1 ]
Liang, Lei [1 ,2 ]
Zong, Chen [1 ]
Lai, Fobao [1 ]
Zhu, Pengxi [3 ]
Liu, Yu [4 ]
Jiang, Jinghua [1 ]
Yang, Yang [1 ]
Gao, Lu [1 ]
Ye, Fei [1 ]
Zhao, Qiudong [1 ]
Li, Rong [1 ]
Han, Zhipeng [1 ]
Wei, Lixin [1 ]
机构
[1] Second Mil Med Univ, Eastern Hepatobiliary Surg Hosp, Tumor Immunol & Gene Therapy Ctr, Shanghai, Peoples R China
[2] Soochow Univ, Coll Med, Suzhou, Peoples R China
[3] Second Mil Med Univ, Chang Hai Hosp, Dept Pharm, Shanghai, Peoples R China
[4] Univ San Francisco, Coll Art & Sci, San Francisco, CA 94117 USA
基金
中国国家自然科学基金;
关键词
aging; mesenchymal stem cells; recruitment; liver injury; Gerotarget; MARROW STROMAL CELLS; HEART-FAILURE; BONE; AUTOPHAGY; AGE; REPERFUSION; GENERATION; MORTALITY; INSIGHTS; CULTURE;
D O I
10.18632/oncotarget.6744
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Mesenchymal stem cells (MSCs) repair tissue injury and may be used to treat immune associated diseases. In carbon tetrachloride (CCl4)-induced liver injury murine model, we administered MSCs. When MSCs were transmitted to young and old mice with liver injury, more MSCs were recruited in old mice. In old mice, inflammation, characterized by TNF-alpha and IL-6, was increased due to hyper-activation and hyper-function of Kupffer cells. Blocking Kupffer cells decreased MSCs migration in old mice. In vitro, Kupffer cells isolated from old mice secreted more inflammatory cytokines and chemokines. Thus, hyper-activation of Kupffer cells in old mice increased recruitment of MSCs after their therapeutic administration.
引用
收藏
页码:1084 / 1095
页数:12
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