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Single-cell RNA-seq analysis of Mesp1-induced skeletal myogenic development.

Biochemical and biophysical research communications (2019-10-09)
Jacqueline S Penaloza, Matthew P Pappas, Hannah R Hagen, Ning Xie, Sunny S K Chan
RESUMEN

The Mesp1 lineage contributes to cardiac, hematopoietic and skeletal myogenic development. Interestingly, muscle stem cells residing in craniofacial skeletal muscles primarily arise from Mesp1+ progenitors, but those in trunk and limb skeletal muscles do not. To gain insights into the difference between the head and trunk/limb muscle developmental processes, we studied Mesp1+ skeletal myogenic derivatives via single-cell RNA-seq and other strategies. Using a doxycycline-inducible Mesp1-expressing mouse embryonic stem cell line, we found that the development of Mesp1-induced skeletal myogenic progenitors can be characterized by dynamic expression of PDGFRα and VCAM1. Single-cell RNA-seq analysis further revealed the heterogeneous nature of these Mesp1+ derivatives, spanning pluripotent and mesodermal to mesenchymal and skeletal myogenic. We subsequently reconstructed the single-cell trajectories of these subpopulations. Our data thereby provide a cell fate projection of Mesp1-induced skeletal myogenesis.

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2- Mercaptoetanol, for molecular biology, suitable for electrophoresis, suitable for cell culture, BioReagent, 99% (GC/titration)
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Triton X-100, laboratory grade
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Ácido L-ascórbico, suitable for cell culture, suitable for plant cell culture, ≥98%
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Proteína LIF recombinante de ratón ESGRO®, ESGRO Leukemia Inhibitory Factor (LIF) supplement for mouse ES cell culture. Each vial contains 10^7 units/ml.
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1-tioglicerol, liquid, BioReagent, suitable for cell culture, ≥97% (titration)
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Paraformaldehyde, reagent grade, crystalline
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Solución de recuento de células Accumaxen cultivo celular esterilizado por filtración DPBS probado, A cell detachment solution of proteolytic, collagenolytic & DNAse enzymes. The reagent is useful for creating single cell suspensions from clumped cell cultures for accurate cell counting, detachment of cells from primary tissue.