| Literature DB >> 28174672 |
Yasuma Yoshizumi1, Hiroshi Yukawa2, Ryoji Iwaki3, Sanae Fujinaka4, Ayano Kanou1, Yuki Kanou1, Tatsuya Yamada1, Shingo Nakagawa1, Tomomi Ohara1, Kenta Nakagiri1, Yusuke Ogihara5, Yoko Tsutsui6, Yumi Hayashi1, Masatoshi Ishigami7, Yoshinobu Baba2, Tetsuya Ishikawa1.
Abstract
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.Entities:
Keywords: Adipose tissue-derived stem cells (ASCs); Concanavalin A (Con A); Fulminant hepatic failure (FHF); Immunomodulatory effect
Year: 2016 PMID: 28174672 PMCID: PMC5225675 DOI: 10.3727/215517916X693159
Source DB: PubMed Journal: Cell Med ISSN: 2155-1790