FGF receptors 1 and 2 control chemically induced injury and compound detoxification in regenerating livers of mice.
FGF receptors 1 and 2 control chemically induced injury and compound detoxification in regenerating livers of mice.
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DOI:
10.1053/j.gastro.2010.06.069
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发表时间:
2010-10
期刊:
影响因子:
29.4
通讯作者:
Werner S
中科院分区:
文献类型:
--
作者:
Böhm F;Speicher T;Hellerbrand C;Dickson C;Partanen JM;Ornitz DM;Werner S
Fibroblast growth factor receptor (FGFR) 4 controls bile acid metabolism and protects the liver from fibrosis, but the roles of FGFR1 and FGFR2 in the adult liver are largely unknown. We investigated the functions and mechanisms of action of these receptors in liver homeostasis, regeneration, and fibrosis. We generated mice with hepatocytes that lack FGFR1 and FGFR2 and subjected them to acute and chronic carbon tetrachloride-induced liver injury and partial hepatectomy; mice were also injected with FGF7. We performed histology, histomorphometry, real-time reverse transcription PCR, and immunoblot analyses. In hepatocytes, loss of FGFR1 and FGFR2 eliminated responsiveness to FGF7 and related FGF family members, but did not affect toxin-induced liver injury and fibrosis. However, mortality after partial hepatectomy increased because of severe hepatocyte necrosis. These effects appeared to be mediated by a failure of hepatocyes to induce the expression of the transcriptional regulators Dbp and Tef upon liver surgery; this affected expression of their target genes, which encode detoxifying cytochrome P450 enzymes. We found that Dbp and Tef expression was directly controlled by FGFR signalling in hepatocytes. As a consequence of the reduced expression of genes that control detoxification, the liver tissue that remained after partial hepatectomy failed to efficiently metabolize endogenous compounds and the drugs applied for anaesthesia/analgesia. We identified a new, cytoprotective effect of FGFR1 and FGFR2 in the regenerating liver and suggest the use of recombinant FGF7 to increase survival of patients after surgical resection of large amounts of liver tissue.
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影响因子:
3.5
作者:
SUZUKI, M;ITOH, T;MITSUI, Y
通讯作者:
MITSUI, Y
DOI:
10.1084/jem.191.11.1975
发表时间:
2000-06-05
期刊:
The Journal of experimental medicine
影响因子:
--
作者:
Latta M;Künstle G;Leist M;Wendel A
通讯作者:
Wendel A
DOI:
10.1038/nrd2792
发表时间:
2009-03
期刊:
Nature reviews. Drug discovery
影响因子:
--
作者:
通讯作者:
--
DOI:
10.1073/pnas.0403412101
发表时间:
2004-07-20
影响因子:
11.1
作者:
Borowiak, M;Garratt, AN;Birchmeier, C
通讯作者:
Birchmeier, C
影响因子:
29
作者:
Gachon, Federic;Olela, Fabienne Fleury;Schibler, Ueli
通讯作者:
Schibler, Ueli