Motor neuron diseases, as the vast majority of neurodegenerative disorders in humans, are incurable conditions that are challenging to study in vitro, owing to the obstacles in obtaining the cell types majorly involved in the pathogenesis. Recent advances in stem cell research, especially in the development of induced pluripotent stem cell (iPSC) technology, have opened up the possibility of generating a substantial amount of disease-specific neuronal cells, including motor neurons and glial cells. The present review analyzes the practical implications of iPSCs, generated from fibroblasts of patients affected by spinal muscular atrophy (SMA), and discusses the challenges in the development and optimization of in vitro disease models. Research on patient-derived disease-specific cells may shed light on the pathological processes behind neuronal dysfunction and death in SMA, thus providing new insights for the development of novel effective therapies.
Pluripotent stem cell-based models of spinal muscular atrophy / E. Frattini, M. Ruggieri, S. Salani, I. Faravelli, C. Zanetta, M. Nizzardo, C. Simone, F. Magri, S. Corti. - In: MOLECULAR AND CELLULAR NEUROSCIENCES. - ISSN 1044-7431. - 64(2015 Jan), pp. 44-50.
|Titolo:||Pluripotent stem cell-based models of spinal muscular atrophy|
FRATTINI, EMANUELE (Corresponding)
MAGRI, FRANCESCA MARIA BENEDETTA (Penultimo)
CORTI, STEFANIA PAOLA (Ultimo)
|Parole Chiave:||cell models; ipscs; neuromuscular diseases; spinal muscular atrophy; animals; fibroblasts; humans; induced pluripotent stem cells; motor neurons; muscular atrophy, spinal; smn complex proteins; stem cell transplantation; molecular biology; cellular and molecular neuroscience; cell biology; medicine (all)|
|Settore Scientifico Disciplinare:||Settore MED/26 - Neurologia|
|Data di pubblicazione:||gen-2015|
|Digital Object Identifier (DOI):||http://dx.doi.org/10.1016/j.mcn.2014.12.005|
|Appare nelle tipologie:||01 - Articolo su periodico|