Literature DB >> 31639376

Stem cell-based therapies for Duchenne muscular dystrophy.

Congshan Sun1, Carlo Serra2, Gabsang Lee3, Kathryn R Wagner2.   

Abstract

Muscular dystrophies are a group of genetic muscle disorders that cause progressive muscle weakness and degeneration. Within this group, Duchenne muscular dystrophy (DMD) is the most common and one of the most severe. DMD is an X chromosome linked disease that occurs to 1 in 3500 to 1 in 5000 boys. The cause of DMD is a mutation in the dystrophin gene, whose encoded protein provides both structural support and cell signaling capabilities. So far, there are very limited therapeutic options available and there is no cure for this disease. In this review, we discuss the existing cell therapy research, especially stem cell-based, which utilize myoblasts, satellite cells, bone marrow cells, mesoangioblasts and CD133+ cells. Finally, we focus on human pluripotent stem cells (hPSCs) which hold great potential in treating DMD. hPSCs can be used for autologous transplantation after being specified to a myogenic lineage. Over the last few years, there has been a rapid development of isolation, as well as differentiation, techniques in order to achieve effective transplantation results of myogenic cells specified from hPSCs. In this review, we summarize the current methods of hPSCs myogenic commitment/differentiation, and describe the current status of hPSC-derived myogenic cell transplantation.
Copyright © 2019 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Duchenne muscular dystrophy (DMD); Myogenic lineage specification; Stem cell therapy; hiPSC

Mesh:

Year:  2019        PMID: 31639376      PMCID: PMC6899334          DOI: 10.1016/j.expneurol.2019.113086

Source DB:  PubMed          Journal:  Exp Neurol        ISSN: 0014-4886            Impact factor:   5.330


  158 in total

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Review 5.  Human muscle production in vitro from pluripotent stem cells: Basic and clinical applications.

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Review 6.  Therapeutic aspects of cell signaling and communication in Duchenne muscular dystrophy.

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