CD36 maintains the gastric mucosa and associates with gastric disease

Jacome-Sosa et al. examine gastric function of CD36, reporting that CD36 knockout mice have altered gland organization and exhibit more fibronectin and inflammatory signaling. The authors find mucosal repair is abrogated due to defective epithelial cell renewal and progenitor cell differentiation, d...

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Main Authors: Miriam Jacome-Sosa, Zhi-Feng Miao, Vivek S. Peche, Edward F. Morris, Ramkumar Narendran, Kathryn M. Pietka, Dmitri Samovski, Hei-Yong G. Lo, Terri Pietka, Andrea Varro, Latisha Love-Gregory, James R. Goldenring, Ondrej Kuda, Eric R. Gamazon, Jason C. Mills, Nada A. Abumrad
Format: Article
Language:English
Published: Nature Portfolio 2021-11-01
Series:Communications Biology
Online Access:https://doi.org/10.1038/s42003-021-02765-z
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author Miriam Jacome-Sosa
Zhi-Feng Miao
Vivek S. Peche
Edward F. Morris
Ramkumar Narendran
Kathryn M. Pietka
Dmitri Samovski
Hei-Yong G. Lo
Terri Pietka
Andrea Varro
Latisha Love-Gregory
James R. Goldenring
Ondrej Kuda
Eric R. Gamazon
Jason C. Mills
Nada A. Abumrad
author_facet Miriam Jacome-Sosa
Zhi-Feng Miao
Vivek S. Peche
Edward F. Morris
Ramkumar Narendran
Kathryn M. Pietka
Dmitri Samovski
Hei-Yong G. Lo
Terri Pietka
Andrea Varro
Latisha Love-Gregory
James R. Goldenring
Ondrej Kuda
Eric R. Gamazon
Jason C. Mills
Nada A. Abumrad
author_sort Miriam Jacome-Sosa
collection DOAJ
description Jacome-Sosa et al. examine gastric function of CD36, reporting that CD36 knockout mice have altered gland organization and exhibit more fibronectin and inflammatory signaling. The authors find mucosal repair is abrogated due to defective epithelial cell renewal and progenitor cell differentiation, due to reduced fatty acid delivery and altered lipid metabolism, and find associations between low CD36 expression and gastric diseases.
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spelling doaj.art-f9ec101e1f814b5fab8d34541185e8f02022-12-21T20:09:11ZengNature PortfolioCommunications Biology2399-36422021-11-014111510.1038/s42003-021-02765-zCD36 maintains the gastric mucosa and associates with gastric diseaseMiriam Jacome-Sosa0Zhi-Feng Miao1Vivek S. Peche2Edward F. Morris3Ramkumar Narendran4Kathryn M. Pietka5Dmitri Samovski6Hei-Yong G. Lo7Terri Pietka8Andrea Varro9Latisha Love-Gregory10James R. Goldenring11Ondrej Kuda12Eric R. Gamazon13Jason C. Mills14Nada A. Abumrad15Center for Human Nutrition, Department of Medicine, Washington University School of MedicineDepartment of Surgical Oncology, Laboratory of Precision Diagnosis and Treatment of Gastrointestinal Tumors, First Hospital of China Medical UniversityCenter for Human Nutrition, Department of Medicine, Washington University School of MedicineCenter for Human Nutrition, Department of Medicine, Washington University School of MedicineCenter for Human Nutrition, Department of Medicine, Washington University School of MedicineCenter for Human Nutrition, Department of Medicine, Washington University School of MedicineCenter for Human Nutrition, Department of Medicine, Washington University School of MedicineDivision of Gastroenterology, Department of Medicine, Washington University School of MedicineCenter for Human Nutrition, Department of Medicine, Washington University School of MedicineInstitute of Translational Medicine, University of LiverpoolDepartment of Pathology & Immunology, Washington University School of MedicineDepartments of Surgery and Cell and Developmental Biology, Vanderbilt University Medical Center and VA Medical CenterInstitute of Physiology, Czech Academy of Sciences, Videnska 1083Division of Genetic Medicine, Vanderbilt University Medical CenterGastroenterology & Hepatology Section, Departments of Medicine and of Molecular and Cellular Biology, Baylor College of MedicineCenter for Human Nutrition, Department of Medicine, Washington University School of MedicineJacome-Sosa et al. examine gastric function of CD36, reporting that CD36 knockout mice have altered gland organization and exhibit more fibronectin and inflammatory signaling. The authors find mucosal repair is abrogated due to defective epithelial cell renewal and progenitor cell differentiation, due to reduced fatty acid delivery and altered lipid metabolism, and find associations between low CD36 expression and gastric diseases.https://doi.org/10.1038/s42003-021-02765-z
spellingShingle Miriam Jacome-Sosa
Zhi-Feng Miao
Vivek S. Peche
Edward F. Morris
Ramkumar Narendran
Kathryn M. Pietka
Dmitri Samovski
Hei-Yong G. Lo
Terri Pietka
Andrea Varro
Latisha Love-Gregory
James R. Goldenring
Ondrej Kuda
Eric R. Gamazon
Jason C. Mills
Nada A. Abumrad
CD36 maintains the gastric mucosa and associates with gastric disease
Communications Biology
title CD36 maintains the gastric mucosa and associates with gastric disease
title_full CD36 maintains the gastric mucosa and associates with gastric disease
title_fullStr CD36 maintains the gastric mucosa and associates with gastric disease
title_full_unstemmed CD36 maintains the gastric mucosa and associates with gastric disease
title_short CD36 maintains the gastric mucosa and associates with gastric disease
title_sort cd36 maintains the gastric mucosa and associates with gastric disease
url https://doi.org/10.1038/s42003-021-02765-z
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