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Generation of a human induced pluripotent stem cell line (iPSC) from peripheral blood mononuclear cells of a patient with a myasthenic syndrome due to mutation in COLQ.

作者信息

Barbeau Susie, Desprat Romain, Eymard Bruno, Martinat Cécile, Lemaitre Jean-Marc, Legay Claire

机构信息

Paris University, SPPIN CNRS 8003 Laboratory, Paris, France.

SAFE-iPSC Facility INGESTEM, Univ. Montpellier, CHU de Montpellier, France.

出版信息

Stem Cell Res. 2020 Dec;49:102106. doi: 10.1016/j.scr.2020.102106. Epub 2020 Dec 2.

Abstract

Congenital myasthenic syndromes (CMS) are a class of inherited disorders affecting the neuromuscular junction, a synapse whose activity is essential for movement. CMS with acetylcholinesterase (AChE) deficiency are caused by mutations in COLQ, a collagen that anchors AChE in the synapse. To study the pathophysiological mechanisms of the disease in human cells, we have generated iPSC from a patient's Peripheral Blood Mononuclear cells (PBMC) by reprogramming these cells using a non-integrative method using Sendai viruses bearing the four Yamanaka factors Oct3/4, Sox2, Klf4, and L-Myc.

摘要

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