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Skeletal Muscle Development

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Cover of 'Skeletal Muscle Development'

Table of Contents

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    Book Overview
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    Chapter 1 Bisulfite Sequencing for DNA Methylation Analysis of Primary Muscle Stem Cells
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    Chapter 2 Whole Genome Chromatin IP-Sequencing (ChIP-Seq) in Skeletal Muscle Cells
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    Chapter 3 Analysis of RNA Expression in Adult Zebrafish Skeletal Muscle
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    Chapter 4 Targeted Lipidomic Analysis of Myoblasts by GC-MS and LC-MS/MS
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    Chapter 5 Measuring Mitochondrial Substrate Utilization in Skeletal Muscle Stem Cells
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    Chapter 6 Microcontact-Printed Hydrogel Microwell Arrays for Clonal Muscle Stem Cell Cultures
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    Chapter 7 Isolation, Culture, and Differentiation of Fibro/Adipogenic Progenitors (FAPs) from Skeletal Muscle
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    Chapter 8 Human Satellite Cell Isolation and Xenotransplantation
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    Chapter 9 Application of Split-GFP Reassembly Assay to Study Myogenesis and Myofusion In Vitro
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    Chapter 10 Myogenic Maturation by Optical-Training in Cultured Skeletal Muscle Cells
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    Chapter 11 Fabrication of Micromolded Gelatin Hydrogels for Long-Term Culture of Aligned Skeletal Myotubes
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    Chapter 12 Quantification of Embryonic Myofiber Development by Immunofluorescence
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    Chapter 13 How to Wire the Diaphragm: Wholemount Staining Methods to Analyze Mammalian Respiratory Innervation
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    Chapter 14 Membrane Repair Assay for Human Skeletal Muscle Cells
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    Chapter 15 Cryoinjury Model for Tissue Injury and Repair in Bioengineered Human Striated Muscle
Attention for Chapter 4: Targeted Lipidomic Analysis of Myoblasts by GC-MS and LC-MS/MS
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Chapter title
Targeted Lipidomic Analysis of Myoblasts by GC-MS and LC-MS/MS
Chapter number 4
Book title
Skeletal Muscle Development
Published in
Methods in molecular biology, August 2017
DOI 10.1007/978-1-4939-7283-8_4
Pubmed ID
Book ISBNs
978-1-4939-7282-1, 978-1-4939-7283-8
Authors

Jordan Blondelle, Jean-Paul Pais de Barros, Fanny Pilot-Storck, Laurent Tiret

Abstract

Lipids represent ∼10% of the cell dry mass and play essential roles in membrane composition and physical properties, energy storage, and signaling pathways. In the developing or the regenerating skeletal muscle, modifications in the content or the flipping between leaflets of membrane lipid components can modulate the fusion capacity of myoblasts, thus constituting one of the regulatory mechanisms underlying myofiber growth. Recently, few genes controlling these qualitative and quantitative modifications have started to be unraveled. The precise functional characterization of these genes requires both qualitative and quantitative evaluations of a global lipid profile. Here, we describe a lipidomic protocol using mass spectrometry, allowing assessing the content of fatty acids, glycerophospholipids, and cholesterol in the routinely used C2C12 mouse myoblast cell line, or in primary cultures of mouse myoblasts.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 13 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 13 100%

Demographic breakdown

Readers by professional status Count As %
Other 2 15%
Professor 2 15%
Student > Doctoral Student 2 15%
Student > Ph. D. Student 2 15%
Unspecified 1 8%
Other 1 8%
Unknown 3 23%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 4 31%
Unspecified 1 8%
Nursing and Health Professions 1 8%
Agricultural and Biological Sciences 1 8%
Social Sciences 1 8%
Other 1 8%
Unknown 4 31%