Hepatic lipocalin 2 promotes liver fibrosis and portal hypertension
Advanced fibrosis and portal hypertension influence short-term mortality. Lipocalin 2 (LCN2) regulates infection response and increases in liver injury. We explored the role of intrahepatic LCN2 in human alcoholic hepatitis (AH) with advanced fibrosis and portal hypertension and in experimental mous...
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Published in | Scientific Reports Vol. 10; no. 1; p. 15558 |
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Main Authors | , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
London
Springer Science and Business Media LLC
23.09.2020
Nature Publishing Group UK |
Subjects | |
Online Access | Get full text |
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Summary: | Advanced fibrosis and portal hypertension influence short-term mortality. Lipocalin 2 (LCN2) regulates infection response and increases in liver injury. We explored the role of intrahepatic LCN2 in human alcoholic hepatitis (AH) with advanced fibrosis and portal hypertension and in experimental mouse fibrosis. We found hepatic
LCN2
expression and serum LCN2 level markedly increased and correlated with disease severity and portal hypertension in patients with AH. In control human livers, LCN2 expressed exclusively in mononuclear cells, while its expression was markedly induced in AH livers, not only in mononuclear cells but also notably in hepatocytes.
Lcn2
−/−
mice were protected from liver fibrosis caused by either ethanol or CCl
4
exposure. Microarray analysis revealed downregulation of matrisome, cell cycle and immune related gene sets in
Lcn2
−/−
mice exposed to CCl
4
, along with decrease in
Timp1
and
Edn1
expression. Hepatic expression of
COL1A1
,
TIMP1
and key
EDN1
system components were elevated in AH patients and correlated with hepatic
LCN2
expressio
n.
In vitro
,
recombinant LCN2 induced
COL1A1
expression. Overexpression of
LCN2
increased HIF1A that in turn mediated
EDN1
upregulation. LCN2 contributes to liver fibrosis and portal hypertension in AH and could represent a new therapeutic target. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 2045-2322 2045-2322 |
DOI: | 10.1038/s41598-020-72172-7 |