The TMEM43 S358L mutation affects cardiac, small intestine, and metabolic homeostasis in a knock-in mouse model

Author:

Orgil Buyan-Ochir12ORCID,Munkhsaikhan Undral3ORCID,Pierre Joseph F.4ORCID,Li Ning125ORCID,Xu Fuyi67,Alberson Neely R.12,Johnson Jason N.12,Wetzel Glenn T.12,Boukens Bastiaan J. D.8,Lu Lu6,Towbin Jeffrey A.129,Purevjav Enkhsaikhan12ORCID

Affiliation:

1. Department of Pediatrics, College of Medicine, University of Tennessee Health Science Center, Memphis, Tennessee, United States

2. Children’s Foundation Research Institute, Le Bonheur Children’s Hospital Memphis, Memphis, Tennessee, United States

3. Department of Physiology, University of Tennessee Health Science Center, Memphis, Tennessee, United States

4. Department of Nutritional Sciences, University of Wisconsin-Madison, Madison, Wisconsin, United States

5. Department of Cardiology, Second Affiliated Hospital, Harbin Medical University, Harbin, People’s Republic of China

6. Department of Genetics, Genomics and Informatics, University of Tennessee Health Science Center, Memphis, Tennessee, United States

7. School of Pharmacy, Binzhou Medical University, Yantai, People’s Republic of China

8. Department of Medical Biology, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands

9. Pediatric Cardiology, St. Jude Children’s Research Hospital, Memphis, Tennessee, United States

Abstract

This manuscript describes the findings of our investigation of cardiac, small intestine, and metabolic features of Tmem43-S358L mouse model. By investigating interorgan pathologies, we uncovered multiple mechanisms of the S358L-induced disease, and these unique mechanisms likely appear to contribute to the disease pathogenesis. We hope our findings are important and novel and open new avenues in the hunting for additional diagnostic and therapeutic targets in subjects carrying TMEM43 mutation.

Funder

University of Tennessee Health Science Center

HHS | NIH | National Heart, Lung, and Blood Institute

Publisher

American Physiological Society

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine,Physiology

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