Pathological alterations in the gastrointestinal tract of a porcine model of DMD

Abstract Background Patients with Duchenne muscular dystrophy (DMD) develop severe skeletal and cardiac muscle pathologies, which result in premature death. Therefore, the current therapeutic efforts are mainly targeted to correct dystrophin expression in skeletal muscle and heart. However, it was r...

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Main Authors: Xiaodong Zou, Hongsheng Ouyang, Daxin Pang, Renzhi Han, Xiaochun Tang
Format: Article
Language:English
Published: BMC 2021-07-01
Series:Cell & Bioscience
Subjects:
Pig
Online Access:https://doi.org/10.1186/s13578-021-00647-9
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spelling doaj-3f290dbccec54069b4285143eb13cf9e2021-07-18T11:38:48ZengBMCCell & Bioscience2045-37012021-07-0111111210.1186/s13578-021-00647-9Pathological alterations in the gastrointestinal tract of a porcine model of DMDXiaodong Zou0Hongsheng Ouyang1Daxin Pang2Renzhi Han3Xiaochun Tang4Jilin Provincial Key Laboratory of Animal Embryo Engineering, College of Animal Sciences, Jilin UniversityJilin Provincial Key Laboratory of Animal Embryo Engineering, College of Animal Sciences, Jilin UniversityJilin Provincial Key Laboratory of Animal Embryo Engineering, College of Animal Sciences, Jilin UniversityDepartment of Surgery, Davis Heart and Lung Research Institute, Biomedical Sciences Graduate Program, Biophysics Graduate Program, The Ohio State University Wexner Medical CenterJilin Provincial Key Laboratory of Animal Embryo Engineering, College of Animal Sciences, Jilin UniversityAbstract Background Patients with Duchenne muscular dystrophy (DMD) develop severe skeletal and cardiac muscle pathologies, which result in premature death. Therefore, the current therapeutic efforts are mainly targeted to correct dystrophin expression in skeletal muscle and heart. However, it was reported that DMD patients may also exhibit gastrointestinal and nutritional problems. How the pathological alterations in gastrointestinal tissues contribute to the disease are not fully explored. Results Here we employed the CRISPR/Cas9 system combined with somatic nuclear transfer technology (SCNT) to establish a porcine model of DMD and explored their pathological alterations. We found that genetic disruption of dystrophin expression led to morphological gastrointestinal tract alterations, weakened the gastrointestinal tract digestion and absorption capacity, and eventually led to malnutrition and gastric dysfunction in the DMD pigs. Conclusions This work provides important insights into the pathogenesis of DMD and highlights the need to consider the gastrointestinal dysfunction as an additional therapeutic target for DMD patients.https://doi.org/10.1186/s13578-021-00647-9CRISPRDuchenne muscular dystrophyGenome editingGastrointestinal tractPigPorcine
collection DOAJ
language English
format Article
sources DOAJ
author Xiaodong Zou
Hongsheng Ouyang
Daxin Pang
Renzhi Han
Xiaochun Tang
spellingShingle Xiaodong Zou
Hongsheng Ouyang
Daxin Pang
Renzhi Han
Xiaochun Tang
Pathological alterations in the gastrointestinal tract of a porcine model of DMD
Cell & Bioscience
CRISPR
Duchenne muscular dystrophy
Genome editing
Gastrointestinal tract
Pig
Porcine
author_facet Xiaodong Zou
Hongsheng Ouyang
Daxin Pang
Renzhi Han
Xiaochun Tang
author_sort Xiaodong Zou
title Pathological alterations in the gastrointestinal tract of a porcine model of DMD
title_short Pathological alterations in the gastrointestinal tract of a porcine model of DMD
title_full Pathological alterations in the gastrointestinal tract of a porcine model of DMD
title_fullStr Pathological alterations in the gastrointestinal tract of a porcine model of DMD
title_full_unstemmed Pathological alterations in the gastrointestinal tract of a porcine model of DMD
title_sort pathological alterations in the gastrointestinal tract of a porcine model of dmd
publisher BMC
series Cell & Bioscience
issn 2045-3701
publishDate 2021-07-01
description Abstract Background Patients with Duchenne muscular dystrophy (DMD) develop severe skeletal and cardiac muscle pathologies, which result in premature death. Therefore, the current therapeutic efforts are mainly targeted to correct dystrophin expression in skeletal muscle and heart. However, it was reported that DMD patients may also exhibit gastrointestinal and nutritional problems. How the pathological alterations in gastrointestinal tissues contribute to the disease are not fully explored. Results Here we employed the CRISPR/Cas9 system combined with somatic nuclear transfer technology (SCNT) to establish a porcine model of DMD and explored their pathological alterations. We found that genetic disruption of dystrophin expression led to morphological gastrointestinal tract alterations, weakened the gastrointestinal tract digestion and absorption capacity, and eventually led to malnutrition and gastric dysfunction in the DMD pigs. Conclusions This work provides important insights into the pathogenesis of DMD and highlights the need to consider the gastrointestinal dysfunction as an additional therapeutic target for DMD patients.
topic CRISPR
Duchenne muscular dystrophy
Genome editing
Gastrointestinal tract
Pig
Porcine
url https://doi.org/10.1186/s13578-021-00647-9
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AT daxinpang pathologicalalterationsinthegastrointestinaltractofaporcinemodelofdmd
AT renzhihan pathologicalalterationsinthegastrointestinaltractofaporcinemodelofdmd
AT xiaochuntang pathologicalalterationsinthegastrointestinaltractofaporcinemodelofdmd
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