Skeletal Muscle Cells Derived from Induced Pluripotent Stem Cells: A Platform for Limb Girdle Muscular Dystrophies

被引：9

作者：

Bruge, Celine ^{[1
,2
,3
]}

Geoffroy, Marine ^{[4
]}

Benabides, Manon ^{[1
,2
,3
]}

Pellier, Emilie ^{[1
,2
,3
]}

Gicquel, Evelyne ^{[4
]}

Dhiab, Jamila ^{[5
]}

Hoch, Lucile ^{[1
,2
,3
]}

Richard, Isabelle ^{[4
]}

Nissan, Xavier ^{[1
,2
,3
]}

机构：

[1] I Stem, CECS, F-91100 Corbeil Essonnes, France

[2] I Stem, INSERM U861, F-91100 Corbeil Essonnes, France

[3] I Stem, UEVE U861, F-91100 Corbeil Essonnes, France

[4] Univ Paris Saclay, Univ Evry, INSERM, INTEGRARE,Genethon, F-91002 Evry, France

[5] Sorbonne Univ, Ctr Rech Myol, Inst Myol, INSERM, F-75013 Paris, France

来源：

BIOMEDICINES | 2022年 / 10卷 / 06期

关键词：

limb girdle muscular dystrophies; induced pluripotent stem cells; skeletal muscle cells; pathological modeling; FUKUTIN-RELATED PROTEIN; ANIMAL-MODELS; GENE-TRANSFER; FUNCTIONAL RESCUE; HUMAN ES; DERIVATION; DIFFERENTIATION; PROGENITORS; GENERATION; MUTATIONS;

D O I：

10.3390/biomedicines10061428

中图分类号：

Q5 [生物化学]; Q7 [分子生物学];

学科分类号：

071010 ; 081704 ;

摘要：

Limb girdle muscular dystrophies (LGMD), caused by mutations in 29 different genes, are the fourth most prevalent group of genetic muscle diseases. Although the link between LGMD and its genetic origins has been determined, LGMD still represent an unmet medical need. Here, we describe a platform for modeling LGMD based on the use of human induced pluripotent stem cells (hiPSC). Thanks to the self-renewing and pluripotency properties of hiPSC, this platform provides a renewable and an alternative source of skeletal muscle cells (skMC) to primary, immortalized, or overexpressing cells. We report that skMC derived from hiPSC express the majority of the genes and proteins that cause LGMD. As a proof of concept, we demonstrate the importance of this cellular model for studying LGMDR9 by evaluating disease-specific phenotypes in skMC derived from hiPSC obtained from four patients.

引用

页数：17

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