RETRACTED: Adipose-derived mesenchymal stem cells ameliorate the inflammatory reaction in CLP-induced septic acute lung injury rats via sTNFR1 (Retracted Article)

被引:10
|
作者
Ding, Xian-Fei [1 ,2 ]
Liang, Huo-Yan [1 ,2 ]
Sun, Jun-Yi [1 ,2 ]
Liu, Shao-Hua [1 ]
Kan, Quan-Cheng [3 ]
Wang, Le-Xin [4 ]
Sun, Tong-Wen [1 ,2 ]
机构
[1] Zhengzhou Univ, Dept Gen ICU, Affiliated Hosp 1, Henan Key Lab Crit Care Med, 1 Jianshe East Rd, Zhengzhou 450052, Henan, Peoples R China
[2] Zhengzhou Univ Translat Med Platform, Acad Med Sci, Zhengzhou, Henan, Peoples R China
[3] Zhengzhou Univ, Affiliated Hosp 1, Pharmaceut Dept, Zhengzhou, Henan, Peoples R China
[4] Charles Sturt Univ, Sch Biomed Sci, Wagga Wagga, NSW, Australia
关键词
acute lung injury; CLP; sepsis; soluble tumor necrosis factor receptor 1; stem cells; STROMAL CELLS; CECAL LIGATION; OXIDATIVE STRESS; TNF-ALPHA; KAPPA-B; SEPSIS; APOPTOSIS; SHOCK; LPS; SURVIVAL;
D O I
10.1002/jcp.28329
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
We hypothesized that the adipose-derived mesenchymal stem cells (ADMSCs), which secrete high amounts of soluble molecules, such as soluble tumor necrosis factor receptor 1 (sTNFR1), may ameliorate sepsis-induced acute lung injury (ALI). A total of 120 male adult Sprague-Dawley rats were separated into four groups: the sham control (SC), sepsis induced by cecal ligation and puncture (CLP), CLP-ADMSCs, and CLP-sTNFR1 small interfering RNA (siRNA) groups; CLP groups underwent CLP and then received 1x10(6) ADMSCs with or without knockdown of sTNFR1 intravenously at 1hr after surgery. Rats were killed at 3, 6, 24, and 48hr after the SC or CLP procedures. 5-Ethynyl-2-deoxyuridine-labeled ADMSCs extensively colonized the lungs at 6, 24, and 72hr after injection. The lung wet/dry (W/D) weight ratios in the CLP group were higher than those in SC group; however, ADMSCs ameliorated the W/D weight ratios following CLP, and this effect was abolished by sTNFR1 siRNA treatment. The levels of serum sTNFR1 and interleukin-10 (IL-10) were higher in the CLP-ADMSCs group and lower in the SC group than in other groups; interestingly, these levels were higher in CLP and CLP-sTNFR1 siRNA groups than in SC group. Tumor necrosis factor- and IL-6 levels increased significantly after CLP, and ADMSCs could alleviate these changes, but the effect was weakened by sTNFR1 siRNA treatment. The lung cell apoptosis and edema levels were consistent with IL-6 levels among all groups. Therapeutically administered ADMSCs secrete sTNFR1, which most likely protects against ALI in septic rats by ameliorating inflammation and lung edema.
引用
收藏
页码:16582 / 16591
页数:10
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