脂肪组织源性干细胞对豆豆蛋白a诱导的小鼠急性肝损伤的免疫调节作用。

Yasuma Yoshizumi, H. Yukawa, Ryoji Iwaki, S. Fujinaka, A. Kanou, Yuki Kanou, Tatsuya Yamada, S. Nakagawa, Tomomi Ohara, Kenta Nakagiri, Y. Ogihara, Y. Tsutsui, Y. Hayashi, M. Ishigami, Y. Baba, Tetsuya Ishikawa
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引用次数: 20

摘要

脂肪组织源性干细胞(ASCs)细胞疗法有望成为暴发性肝衰竭(FHF)治疗的候选药物,这是由过度免疫反应引起的。为了评价ASCs对FHF的治疗作用,我们在小鼠模型上详细考察了ASCs的体内和体外免疫调节作用。通过观察ASCs在三种丝裂原(phorbol 12-肉豆蔻酸13-乙酸酯(PMA) +离子霉素、魔芋蛋白A (ConA)和脂多糖(LPS))刺激下对淋巴单核细胞(LMCs)增殖的影响,探讨ASCs的体外作用。在PMA +离子霉素刺激和ConA刺激的情况下,ASCs有效抑制LMCs的增殖,并呈剂量依赖性,但在LPS刺激的情况下则没有。在ConA诱导的小鼠FHF模型中,观察了移植ASCs的体内作用。ASCs移植明显减轻了cona给药小鼠的ALT水平和组织学炎症变化。肝脏mRNA表达谱分析显示,asc移植小鼠肝脏细胞因子Il-6、Il-10、Ifn-γ、Tnf-α表达下调,细胞表面标志物Cd3γ、Cd4、Cd8α、Cd11b、Cd11c表达下调。体外和体内小鼠模型均证实了ASCs的免疫调节和治疗作用。提示ASCs细胞治疗有利于FHF的治疗。
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Immunomodulatory Effects of Adipose Tissue-Derived Stem Cells on Concanavalin A-Induced Acute Liver Injury in Mice.
Cell therapy with adipose tissue-derived stem cells (ASCs) is expected to be a candidate for the treatment of fulminant hepatic failure (FHF), which is caused by excessive immune responses. In order to evaluate the therapeutic effects of ASCs on FHF, the in vitro and in vivo immunomodulatory effects of ASCs were examined in detail in the mouse model. The in vitro effects of ASCs were examined by assessing their influence on the proliferation of lymphomononuclear cells (LMCs) stimulated with three kinds of mitogens: phorbol 12-myristate 13-acetate (PMA) plus ionomycin, concanavalin A (ConA), and lipopolysaccharide (LPS). The proliferation of LMCs was efficiently suppressed in a dose-dependent manner by ASCs in the cases of PMA plus ionomycin stimulation and ConA stimulation, but not in the case of LPS stimulation. The in vivo effects of transplanted ASCs were examined in the murine FHF model induced by ConA administration. The ALT levels and histological inflammatory changes in the ConA-administered mice were apparently relieved by the transplantation of ASCs. The analysis of mRNA expression patterns in the livers indicated that the expressions of the cytokines such as Il-6, Il-10, Ifn-γ, and Tnf-α, and the cell surface markers such as Cd3γ, Cd4, Cd8α, Cd11b, and Cd11c were downregulated in the ASC-transplanted mice. The immunomodulatory and therapeutic effects of ASCs were confirmed in the mouse model both in vitro and in vivo. These suggest that the cell therapy with ASCs is beneficial for the treatment of FHF.
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Cell medicine
Cell medicine MEDICINE, RESEARCH & EXPERIMENTAL-
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