The Neuromuscular Disorder Mediated by Extracellular Vesicles in Amyotrophic Lateral Sclerosis.
Elisabetta CarataMarco MuciSimona Di GiulioTiziano Di GiulioStefania MarianoElisa PanzariniPublished in: Current issues in molecular biology (2024)
Amyotrophic lateral sclerosis (ALS) represents a neurodegenerative disorder characterized by the progressive loss of both upper and lower motor neurons, resulting in muscular atrophy and eventual paralysis. While much research has concentrated on investigating the impact of major mutations associated with ALS on motor neurons and central nervous system (CNS) cells, recent studies have unveiled that ALS pathogenesis extends beyond CNS imbalances, encompassing dysregulation in other tissues such as skeletal muscle. Evidence from animal models and patients supports this broader perspective. Skeletal muscle, once considered solely as an effector organ, is now recognized as possessing significant secretory activity capable of influencing motor neuron survival. However, the precise cellular and molecular mechanisms underlying the detrimental effects observed in muscle and its associated structures in ALS remain poorly understood. Additionally, emerging data suggest that extracellular vesicles (EVs) may play a role in the establishment and function of the neuromuscular junction (NMJ) under both physiological and pathological conditions and in wasting and regeneration of skeletal muscles, particularly in neurodegenerative diseases like ALS. This review aims to explore the key findings about skeletal muscle involvement in ALS, shedding light on the potential underlying mechanisms and contributions of EVs and their possible application for the design of biosensors.
Keyphrases
- amyotrophic lateral sclerosis
- skeletal muscle
- insulin resistance
- end stage renal disease
- stem cells
- spinal cord
- multiple sclerosis
- chronic kidney disease
- induced apoptosis
- ejection fraction
- blood brain barrier
- newly diagnosed
- risk assessment
- high resolution
- metabolic syndrome
- electronic health record
- dendritic cells
- adipose tissue
- prognostic factors
- cell proliferation
- patient reported outcomes
- mass spectrometry
- high intensity