Jove
Visualize
Contact Us

Related Concept Videos

Satellite Stem Cells and Muscular Dystrophy01:21

Satellite Stem Cells and Muscular Dystrophy

2.4K
Satellite stem cells or myosatellite cells are quiescent stem cells that Alexander Mauro first identified in 1961. These cells are located between the sarcolemma, the plasma membrane of muscle fibers, and the basal lamina, the connective tissue sheath covering it. These mononucleated cells are activated in response to muscle injury, can transform into myoblasts, and may form or repair muscle fibers. Myosatellite cells can provide additional myonuclei for muscle regeneration or return to a...
2.4K
Mutations01:39

Mutations

94.5K
Overview
94.5K
Role of Myosin in Cell Migration01:18

Role of Myosin in Cell Migration

3.4K
Myosins are multimeric motor proteins involved in various cellular processes such as migration, adhesion, and proliferation. Myosin II is the most common type in animal cells, which binds and cross-links actin filaments.
Myosin II  is a hexamer comprising two heavy chains with globular heads and coiled-coil tails, two regulatory light chains, and two essential light chains. The ATPase sites on the myosin heads hydrolyze ATP, and the released phosphate generates the force for contraction....
3.4K
iPS Cell Differentiation01:22

iPS Cell Differentiation

3.1K
The ability of induced pluripotent stem cells or iPSCs to differentiate into most body cell types has stimulated repair and regenerative medicine research over the past few decades. iPSC-derived blood cells, hepatocytes, beta islet cells, cardiomyocytes, neurons, and other cell types can repair injuries or regenerate damaged tissue in diseases such as diabetes and neurodegenerative disorders.
3.1K
B Cell Activation and Differentiation01:24

B Cell Activation and Differentiation

16.7K
The adaptive immune response, a sophisticated defense mechanism, relies on the activation and differentiation of B lymphocytes, or B cells. These processes enable our bodies to mount a tailored response against specific pathogens such as bacteria, free virus particles, toxins, and parasites.
When naive B cells encounter a specific antigen that can bind to the B cell receptor (BCR) on their surface, they undergo sensitization to respond to the antigen's presence. Sensitization begins with...
16.7K
Cancers Originate from Somatic Mutations in a Single Cell02:21

Cancers Originate from Somatic Mutations in a Single Cell

14.9K
Cancer arises from mutations in the critical genes that allow healthy cells to escape cell cycle regulation and acquire the ability to proliferate indefinitely. Though originating from a single mutation event in one of the originator cells, cancer progresses when the mutant cell lines continue to gain more and more mutations, and finally, become malignant. For example, chronic myelogenous leukemia (CML) develops initially as a non-lethal increase in white blood cells, which progressively...
14.9K

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Filamin C Modulates Cellular Mechanoresponse Through Focal Adhesion Turnover and Actin Stabilization.

Cytoskeleton (Hoboken, N.J.)·2026
Same author

Lung Tissue RNA Sequencing Shows Dysregulation of the Bronchial Epithelium in a Rat Model of Chronic Thromboembolic Pulmonary Hypertension.

Bulletin of experimental biology and medicine·2026
Same author

[Sample Preparation and Sequencing Efficiency of microRNA Libraries from Pituitary Adenoma Tissue and Blood Plasma of Patients with Acromegaly for the Illumina Platform].

Molekuliarnaia biologiia·2025
Same author

[Phenotypic heterogeneity of Charcot-Marie-Tooth type 2A disease associated with the c.1091G>C missense mutation (p.Arg364Pro) in the MFN2 gene].

Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova·2025
Same author

<i>Ex vivo</i> model of pathological calcification of human aortic valve.

Frontiers in cardiovascular medicine·2024
Same author

Flnc expression impacts mitochondrial function, autophagy, and calcium handling in C2C12 cells.

Experimental cell research·2024
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Video

Updated: Feb 5, 2026

Modeling Myotonic Dystrophy 1 in C2C12 Myoblast Cells
09:39

Modeling Myotonic Dystrophy 1 in C2C12 Myoblast Cells

Published on: July 29, 2016

16.0K

THE ROLE OF LMNA MUTATIONS IN MYOGENIC DIFFERENTIATION OF PRIMARY SATELLITE CELLS AND C2C12 CELLS.

K I Perepelina, N A Smolina, A S Zabirnik

    Tsitologiia
    |September 11, 2018
    PubMed
    Summary
    This summary is machine-generated.

    Mutations in nuclear lamins (LMNA gene) impair muscle cell differentiation and myotube formation. These genetic changes affect key stages of myogenesis, impacting cellular structure and function.

    More Related Videos

    Isolation and Quantitative Immunocytochemical Characterization of Primary Myogenic Cells and Fibroblasts from Human Skeletal Muscle
    11:22

    Isolation and Quantitative Immunocytochemical Characterization of Primary Myogenic Cells and Fibroblasts from Human Skeletal Muscle

    Published on: January 12, 2015

    16.7K
    Preparation of Primary Myogenic Precursor Cell/Myoblast Cultures from Basal Vertebrate Lineages
    07:51

    Preparation of Primary Myogenic Precursor Cell/Myoblast Cultures from Basal Vertebrate Lineages

    Published on: April 30, 2014

    21.2K

    Related Experiment Videos

    Last Updated: Feb 5, 2026

    Modeling Myotonic Dystrophy 1 in C2C12 Myoblast Cells
    09:39

    Modeling Myotonic Dystrophy 1 in C2C12 Myoblast Cells

    Published on: July 29, 2016

    16.0K
    Isolation and Quantitative Immunocytochemical Characterization of Primary Myogenic Cells and Fibroblasts from Human Skeletal Muscle
    11:22

    Isolation and Quantitative Immunocytochemical Characterization of Primary Myogenic Cells and Fibroblasts from Human Skeletal Muscle

    Published on: January 12, 2015

    16.7K
    Preparation of Primary Myogenic Precursor Cell/Myoblast Cultures from Basal Vertebrate Lineages
    07:51

    Preparation of Primary Myogenic Precursor Cell/Myoblast Cultures from Basal Vertebrate Lineages

    Published on: April 30, 2014

    21.2K

    Area of Science:

    • Cell Biology
    • Molecular Biology
    • Genetics

    Background:

    • Nuclear lamins, structural proteins of the nuclear lamina, are increasingly recognized for roles beyond structural support, including chromatin organization and gene transcription.
    • Mutations in the LMNA gene cause laminopathies, a group of diseases primarily affecting mesenchymal tissues.
    • The precise mechanisms by which nuclear lamins regulate cell differentiation are not fully understood.

    Purpose of the Study:

    • To investigate the impact of specific LMNA gene mutations on muscle differentiation in primary satellite cells and the C2C12 cell line.
    • To elucidate how LMNA mutations affect cellular morphology, gene expression, and myogenesis.

    Main Methods:

    • Genetic modification of satellite cells and C2C12 cells using lentiviral constructs encoding LMNA G232E (Emery-Dreyfus muscular dystrophy) and LMNA R571S (dilated cardiomyopathy) mutations.
    • Assessment of cellular morphology via immunofluorescence.
    • Quantitative real-time PCR (qPCR) to analyze the expression levels of myogenic genes.

    Main Results:

    • LMNA mutations significantly reduced the differentiation, fusion, and myotube formation capabilities of muscle cells.
    • The observed differentiation defects correlated with increased expression of early-stage myogenesis markers and decreased expression of late-stage markers.
    • Immunofluorescence revealed altered cellular morphology in cells with LMNA mutations.

    Conclusions:

    • Mutations in the LMNA gene negatively influence muscle differentiation by disrupting the temporal regulation of myogenesis.
    • Nuclear lamins play a critical role in regulating muscle cell differentiation, and their dysfunction can lead to myopathies.