Impaired liver regeneration in mice by lipopolysaccharide via TNF-α/kallikrein-mediated activation of latent TGF-β

Kuniharu Akita, Masataka Okuno, Masamichi Enya, Shoko Imai, Hisataka Moriwaki, Norifumi Kawada, Yasuhiro Suzuki, Soichi Kojima

研究成果: Article査読

69 被引用数 (Scopus)

抄録

Background & Aims: Because impaired regeneration after surgical treatment of the liver is influenced by circulating endotoxin, the underlying molecular mechanism was investigated. Methods: Lipopolysaccharide (LPS) was injected intraperitoneally into mice, followed 24 hours later by 67% partial hepatectomy. We measured serum tumor necrosis factor (TNF) α levels as well as proliferating cell nuclear antigen labeling index, transforming growth factor (TGF) β expression, and plasma kallikrein (PLK) activities in regenerating livers. We also examined the effect of LPS, TNF-α, and PLK on latent TGF-β activation in homotypic and heterotypic cultures of rat or mouse hepatic stellate cells and Kupffer cells. Results: Serum TNF-α levels increased after LPS (500 ng/g body wt) injection and after partial hepatectomy, accompanying TGF-β-mediated suppression of hepatic proliferating cell nuclear antigen labeling index. This suppression was mimicked by a combination of preadministration of 50 ng/g body wt LPS and postoperative administration of 5 ng/g body wt TNF-α. In vitro, LPS stimulated Kupffer cells to secrete TNF-α, which enhanced PLK activity on the hepatic stellate cell surface through increasing PLK binding, thereby inducing proteolytic activation of latent TGF-β and its autoinduction. Blockade of TGF-β, TNF-α, or PLK activity prevented LPS-induced impaired regeneration in vivo. Conclusions: LPS provokes TNF-α/PLK-mediated proteolytic activation of latent TGF-β in hepatic stellate cells, leading to impaired liver regeneration after partial hepatectomy.

本文言語English
ページ(範囲)352-364
ページ数13
ジャーナルGastroenterology
123
1
DOI
出版ステータスPublished - 2002
外部発表はい

ASJC Scopus subject areas

  • Hepatology
  • Gastroenterology

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