دورية أكاديمية

Cdon ablation in motor neurons causes age‐related motor neuron degeneration and impaired sciatic nerve repair

التفاصيل البيبلوغرافية
العنوان: Cdon ablation in motor neurons causes age‐related motor neuron degeneration and impaired sciatic nerve repair
المؤلفون: Sunghee Kim, Subin An, Jinwoo Lee, Yideul Jeong, Chang‐Lim You, Hyebeen Kim, Ju‐Hyeon Bae, Chae‐Eun Yun, Dongryul Ryu, Gyu‐Un Bae, Jong‐Sun Kang
المصدر: Journal of Cachexia, Sarcopenia and Muscle, Vol 14, Iss 5, Pp 2239-2252 (2023)
بيانات النشر: Wiley, 2023.
سنة النشر: 2023
المجموعة: LCC:Diseases of the musculoskeletal system
LCC:Human anatomy
مصطلحات موضوعية: Amyotrophic lateral sclerosis, Cdon, Motor neuron, Muscle atrophy, Neuromuscular junction, Diseases of the musculoskeletal system, RC925-935, Human anatomy, QM1-695
الوصف: Abstract Background The functional deterioration and loss of motor neurons are tightly associated with degenerative motor neuron diseases and aging‐related muscle wasting. Motor neuron diseases or aging‐related muscle wasting in turn contribute to increased risk of adverse health outcomes in the elderly. Cdon (cell adhesion molecule‐downregulated oncogene) belongs to the immunoglobulin superfamily of cell adhesion molecule and plays essential roles in multiple signalling pathways, including sonic hedgehog (Shh), netrin, and cadherin‐mediated signalling. Cdon as a Shh coreceptor plays a critical role in motor neuron specification during embryonic development. However, its role in adult motor neuron function is unknown. Methods Hb9‐Cre recombinase‐driven motor neuron‐specific Cdon deficient mice (mnKO) and a compound mutant mice (mnKO::SOD1G93A) were generated to investigate the role of Cdon in motor neuron degeneration. Motor neuron regeneration was examined by using a sciatic nerve crush injury model. To investigate the phenotype, physical activity, compound muscle action potential, immunostaining, and transmission electron microscopy were carried out. In the mechanism study, RNA sequencing and RNA/protein analyses were employed. Results Mice lacking Cdon in motor neurons exhibited middle age onset lethality and aging‐related decline in motor function. In the sciatic nerve crush injury model, mnKO mice exhibited an impairment in motor function recovery evident by prolonged compound muscle action potential duration (4.63 ± 0.35 vs. 3.93 ± 0.22 s for f/f, P
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 2190-6009
2190-5991
Relation: https://doaj.org/toc/2190-5991; https://doaj.org/toc/2190-6009
DOI: 10.1002/jcsm.13308
URL الوصول: https://doaj.org/article/c0e147277b91460d85118f3f0d19ecb2
رقم الأكسشن: edsdoj.0e147277b91460d85118f3f0d19ecb2
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:21906009
21905991
DOI:10.1002/jcsm.13308