MiR130b from Schlafen4


Journal

Gut
ISSN: 1468-3288
Titre abrégé: Gut
Pays: England
ID NLM: 2985108R

Informations de publication

Date de publication:
10 2020
Historique:
received: 31 03 2019
revised: 26 12 2019
accepted: 09 01 2020
pubmed: 26 1 2020
medline: 10 4 2021
entrez: 26 1 2020
Statut: ppublish

Résumé

The myeloid differentiation factor Schlafen4 (Slfn4) marks a subset of myeloid-derived suppressor cells (MDSCs) in the stomach during To identify the gene products expressed by Slfn4 We performed transcriptome analyses for both coding genes (mRNA by RNA-Seq) and non-coding genes (microRNAs using NanoString nCounter) using flow-sorted SLFN4 MicroRNA analysis identified an increase in MiR130b in gastric SLFN4 Taken together, MiR130b plays an essential role in MDSC function and supports metaplastic transformation.

Identifiants

pubmed: 31980446
pii: gutjnl-2019-318817
doi: 10.1136/gutjnl-2019-318817
pmc: PMC7377952
mid: NIHMS1565878
doi:

Substances chimiques

Carrier Proteins 0
Interferon-alpha 0
MIRN130 microRNA, mouse 0
MicroRNAs 0
schlafen-4 protein, mouse 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

1750-1761

Subventions

Organisme : NIDDK NIH HHS
ID : P01 DK062041
Pays : United States
Organisme : NIDDK NIH HHS
ID : P30 DK034933
Pays : United States
Organisme : NIDDK NIH HHS
ID : P30 DK041301
Pays : United States
Organisme : NIDDK NIH HHS
ID : R01 DK118563
Pays : United States

Informations de copyright

© Author(s) (or their employer(s)) 2020. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: None declared.

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Auteurs

Lin Ding (L)

Internal Medicine-Gastroenterology, University of Michigan, Ann Arbor, Michigan, USA.
Medicine, University of Arizona, Tucson, Arizona, USA.

Qian Li (Q)

Department of Gastroenterology, Xiangya Hospital Central South University, Changsha, Hunan, China.

Jayati Chakrabarti (J)

Pharmacology and Systems Physiology, University of Cincinnati, Cincinnati, Ohio, USA.

Andres Munoz (A)

Medicine, University of Arizona, Tucson, Arizona, USA.

Emmanuelle Faure-Kumar (E)

Medicine-Digestive Diseases, UCLA, Los Angeles, California, USA.

Ramon Ocadiz-Ruiz (R)

Internal Medicine-Gastroenterology, University of Michigan, Ann Arbor, Michigan, USA.

Nataliya Razumilava (N)

Internal Medicine-Gastroenterology, University of Michigan, Ann Arbor, Michigan, USA.

Guiying Zhang (G)

Department of Gastroenterology, Xiangya Hospital Central South University, Changsha, Hunan, China.

Michael H Hayes (MH)

Internal Medicine-Gastroenterology, University of Michigan, Ann Arbor, Michigan, USA.

Ricky A Sontz (RA)

Medicine, University of Arizona, Tucson, Arizona, USA.

Zoe Elena Mendoza (ZE)

Medicine, University of Arizona, Tucson, Arizona, USA.

Swapna Mahurkar (S)

Medicine-Digestive Diseases, UCLA, Los Angeles, California, USA.

Joel K Greenson (JK)

Pathology, University of Michigan, Ann Arbor, Michigan, USA.

Guillermo Perez-Perez (G)

New York University School of Medicine, New York, New York, USA.

Nguyen Thi Hong Hanh (NTH)

Dinh Tien Hoang Medical Institute, VUSTA, Hanoi, Viet Nam.

Yana Zavros (Y)

Pharmacology and Systems Physiology, University of Cincinnati, Cincinnati, Ohio, USA.

Linda C Samuelson (LC)

Molecular and Integrative Physiology, University of Michigan, Ann Arbor, Michigan, USA.

Dimitrios Iliopoulos (D)

Medicine-Digestive Diseases, UCLA, Los Angeles, California, USA.

Juanita L Merchant (JL)

Internal Medicine-Gastroenterology, University of Michigan, Ann Arbor, Michigan, USA jmerchant@email.arizona.edu.
Medicine, University of Arizona, Tucson, Arizona, USA.
Molecular and Integrative Physiology, University of Michigan, Ann Arbor, Michigan, USA.

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