Arachidonate 12S-lipoxygenase of platelet-type in hepatic stellate cells of methionine and choline-deficient diet-fed mice.
Animals
Arachidonate 12-Lipoxygenase
/ genetics
Choline
/ metabolism
Choline Deficiency
/ metabolism
Diet
/ adverse effects
Disease Models, Animal
Hepatic Stellate Cells
/ enzymology
Isoenzymes
Liver
/ enzymology
Male
Methionine
/ deficiency
Mice
Mice, Inbred C57BL
Non-alcoholic Fatty Liver Disease
/ enzymology
arachidonic acid
hepatic stellate cells
non-alcoholic steatohepatitis (NASH)
platelet-type 12S-lipoxygenase
α-smooth muscle actin
Journal
Journal of biochemistry
ISSN: 1756-2651
Titre abrégé: J Biochem
Pays: England
ID NLM: 0376600
Informations de publication
Date de publication:
01 Nov 2020
01 Nov 2020
Historique:
received:
16
01
2020
accepted:
22
05
2020
pubmed:
4
6
2020
medline:
4
3
2021
entrez:
4
6
2020
Statut:
ppublish
Résumé
A role of 12-lipoxygenase in the progression of non-alcoholic steatohepatitis (NASH) is suggested, although the underlying mechanism is not entirely understood. The catalytic activity of 12S-lipoxygenase that was hardly observed in liver cytosol of normal chow-fed mice was clearly detectable in that of NASH model mice prepared by feeding a methionine and choline-deficient (MCD) diet. The product profile, substrate specificity and immunogenicity indicated that the enzyme was the platelet-type isoform. The expression levels of mRNA and protein of platelet-type 12S-lipoxygenase in the liver of MCD diet-fed mice were significantly increased compared with those of normal chow-fed mice. Immunohistochemical analysis showed that platelet-type 12S-lipoxygenase colocalized with α-smooth muscle actin as well as vitamin A in the cells distributing along liver sinusoids. These results indicate that the expression level of platelet-type 12S-lipoxygenase in hepatic stellate cells was increased during the cell activation in MCD diet-fed mice, suggesting a possible role of the enzyme in pathophysiology of liver fibrosis.
Identifiants
pubmed: 32492133
pii: 5850865
doi: 10.1093/jb/mvaa062
doi:
Substances chimiques
Isoenzymes
0
Methionine
AE28F7PNPL
Arachidonate 12-Lipoxygenase
EC 1.13.11.31
Choline
N91BDP6H0X
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
455-463Informations de copyright
© The Author(s) 2020. Published by Oxford University Press on behalf of the Japanese Biochemical Society. All rights reserved.