Chen Xiaoming,Zhu Yu,Zheng Danyang,Li Tao,Liu Liangming.Poly(I:C)-pretreated MSCs protect intestinal barrier function in rats after sepsis[J].J Amry Med Univ (J Third Mil Med Univ),2016,38(09):959-963.
Chen Xiaoming,Zhu Yu,Zheng Danyang,Li Tao,Liu Liangming.Poly(I:C)-pretreated MSCs protect intestinal barrier function in rats after sepsis[J].J Amry Med Univ (J Third Mil Med Univ),2016,38(09):959-963.DOI:
Objective To determine the protective effects of mesenchymal stem cells (MSCs) and polyriboinosinic: polyribocytidylic acid [poly(I:C)
]
pre-stimulated MSCs on the intestinal barrier function in sepsis rats. Methods The sepsis model of rats was established with cecal ligation and puncture (CLP). SD rats were randomly divided into normal control
cells/animal) and ploy(I:C) pre-stimulated MSCs+CT groups [MSC was pre-stimulated by poly (I:C) with 20 μg/mL for 24 h
]
. The intestinal permeability
levels of blood endotoxin and D-lactic acid (D-Lac)
intestinal morphology and animal survival time and survival rates were observed. Results Compared with normal control group
the levels of intestinal permeability
D-Lac and endotoxin were significantly increased in sepsis rats (P0.01). The pathological observation showed that the intestinal villi were obviously decreased
the inflammatory cells and red blood cells were significantly increased. In 3 d after conventional treatment
the intestinal barrier function were slightly improved
the levels of blood D-Lac and endotoxin were slightly reduced
and the intestinal injury had some extent of alleviation. MSCs treatment was better than the CT treatment. What’s more
poly(I:C) pre-stimulation significantly enhanced the protective effect of MSCs along on intestinal barrier function. The concentrations of blood D-Lac and endotoxin were significantly reduced in poly(I:C) pre-stimulated MSCs group than in MSCs group (P0.05). The intestinal glands and villi were obviously increased and the inflammatory cells were significantly decreased in this group. Conclusion Poly(I:C) pre-stimulation enhances the protective effects of MSCs on intestinal barrier function in sepsis rats.