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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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 |
work_keys_str_mv |
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