Mice lacking α-, β1- and β2-syntrophins exhibit diminished function and reduced dystrophin expression in both cardiac and skeletal muscle
| Autor: | Nicholas P. Whitehead, Kenneth L. Bible, Stanley C. Froehner, Marvin E. Adams, Min Jeong Kim |
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| Rok vydání: | 2018 |
| Předmět: |
0301 basic medicine
Cardiac function curve Gene isoform medicine.medical_specialty Muscle Proteins Biology Motor Activity Dystrophin 03 medical and health sciences Mice Internal medicine Genetics medicine Animals Protein Isoforms Muscle Skeletal Molecular Biology Genetics (clinical) Syntrophin Mice Knockout Sarcolemma Myocardium Calcium-Binding Proteins Cardiac muscle Skeletal muscle Signal transducing adaptor protein Membrane Proteins Heart General Medicine Mice Inbred C57BL 030104 developmental biology medicine.anatomical_structure Endocrinology Dystrophin-Associated Proteins biology.protein General Article |
| Zdroj: | Human molecular genetics. 28(3) |
| ISSN: | 1460-2083 |
| Popis: | Syntrophins are a family of modular adaptor proteins that are part of the dystrophin protein complex, where they recruit and anchor a variety of signaling proteins. Previously we generated mice lacking α- and/or β2-syntrophin but showed that in the absence of one isoform, other syntrophin isoforms can partially compensate. Therefore, in the current study, we generated mice that lacked α, β1 and β2-syntrophins [triple syntrophin knockout (tKO) mice] and assessed skeletal and cardiac muscle function. The tKO mice showed a profound reduction in voluntary wheel running activity at both 6 and 12 months of age. Function of the tibialis anterior was assessed in situ and we found that the specific force of tKO muscle was decreased by 20-25% compared with wild-type mice. This decrease was accompanied by a shift in fiber-type composition from fast 2B to more oxidative fast 2A fibers. Using echocardiography to measure cardiac function, it was revealed that tKO hearts had left ventricular cardiac dysfunction and were hypertrophic, with a thicker left ventricular posterior wall. Interestingly, we also found that membrane-localized dystrophin expression was lower in both skeletal and cardiac muscles of tKO mice. Since dystrophin mRNA levels were not different in tKO, this finding suggests that syntrophins may regulate dystrophin trafficking to, or stabilization at, the sarcolemma. These results show that the loss of all three major muscle syntrophins has a profound effect on exercise performance, and skeletal and cardiac muscle dysfunction contributes to this deficiency. |
| Databáze: | OpenAIRE |
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