Blocking integrin α
Animals
Antibodies, Monoclonal
/ immunology
CD4-Positive T-Lymphocytes
/ immunology
Cell Adhesion Molecules
/ antagonists & inhibitors
Diet, Western
/ adverse effects
Disease Models, Animal
Gastrointestinal Microbiome
/ genetics
Humans
Integrins
/ antagonists & inhibitors
Intestinal Mucosa
/ immunology
Liver
/ immunology
Male
Mice
Mice, Knockout
Mucoproteins
/ antagonists & inhibitors
Non-alcoholic Fatty Liver Disease
/ drug therapy
RNA, Ribosomal, 16S
/ genetics
Receptors, Cell Surface
/ deficiency
Epithelial barrier
Gut permeability
Inflammation
Microbiota
Non-alcoholic fatty liver disease
Journal
Journal of hepatology
ISSN: 1600-0641
Titre abrégé: J Hepatol
Pays: Netherlands
ID NLM: 8503886
Informations de publication
Date de publication:
11 2020
11 2020
Historique:
received:
11
07
2019
revised:
29
04
2020
accepted:
25
05
2020
pubmed:
17
6
2020
medline:
14
10
2021
entrez:
17
6
2020
Statut:
ppublish
Résumé
The heterodimeric integrin receptor α Male littermate F11r WD-fed knockout mice developed NASH and had increased hepatic and intestinal α These findings establish α Non-alcoholic steatohepatitis (NASH) is an advanced and progressive form of non-alcoholic fatty liver disease (NAFLD), and despite its growing incidence no therapies currently exist to halt NAFLD progression. Herein, we show that blocking integrin receptor α
Sections du résumé
BACKGROUND & AIMS
The heterodimeric integrin receptor α
METHODS
Male littermate F11r
RESULTS
WD-fed knockout mice developed NASH and had increased hepatic and intestinal α
CONCLUSIONS
These findings establish α
LAY SUMMARY
Non-alcoholic steatohepatitis (NASH) is an advanced and progressive form of non-alcoholic fatty liver disease (NAFLD), and despite its growing incidence no therapies currently exist to halt NAFLD progression. Herein, we show that blocking integrin receptor α
Identifiants
pubmed: 32540177
pii: S0168-8278(20)30375-5
doi: 10.1016/j.jhep.2020.05.047
pmc: PMC7839272
mid: NIHMS1603613
pii:
doi:
Substances chimiques
Antibodies, Monoclonal
0
Cell Adhesion Molecules
0
F11r protein, mouse
0
Integrins
0
MADCAM1 protein, human
0
Madcam1 protein, mouse
0
Mucoproteins
0
RNA, Ribosomal, 16S
0
Receptors, Cell Surface
0
integrin alpha4beta7
0
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
1013-1022Subventions
Organisme : NIAID NIH HHS
ID : R03 AI138792
Pays : United States
Organisme : NIDDK NIH HHS
ID : R01 DK044234
Pays : United States
Organisme : NIDDK NIH HHS
ID : R01 DK062277
Pays : United States
Organisme : NIDDK NIH HHS
ID : P30 DK120531
Pays : United States
Organisme : NIDDK NIH HHS
ID : R01 DK072564
Pays : United States
Organisme : NIDDK NIH HHS
ID : K01 DK110264
Pays : United States
Organisme : NIDDK NIH HHS
ID : R01 DK100287
Pays : United States
Organisme : NIDDK NIH HHS
ID : R01 DK061379
Pays : United States
Organisme : NIDDK NIH HHS
ID : R01 DK111678
Pays : United States
Organisme : NIH HHS
ID : K01 OD023034
Pays : United States
Organisme : NCI NIH HHS
ID : R01 CA204586
Pays : United States
Organisme : NIAID NIH HHS
ID : R21 AI143454
Pays : United States
Organisme : NIDDK NIH HHS
ID : P30 DK034933
Pays : United States
Informations de copyright
Copyright © 2020 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved.
Déclaration de conflit d'intérêts
Conflict of interest The authors declare no conflicts of interest that pertain to this work. Please refer to the accompanying ICMJE disclosure forms for further details.
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