Jove
Visualize
Contact Us

Related Concept Videos

Abnormal Proliferation02:23

Abnormal Proliferation

4.7K
Under normal conditions, most adult cells remain in a non-proliferative state unless stimulated by internal or external factors to replace lost cells. Abnormal cell proliferation is a condition in which the cell's growth exceeds and is uncoordinated with normal cells. In such situations, cell division persists in the same excessive manner even after cessation of the stimuli, leading to persistent tumors. The tumor arises from the damaged cells that replicate to pass the damage to the...
4.7K
Satellite Stem Cells and Muscular Dystrophy01:21

Satellite Stem Cells and Muscular Dystrophy

2.1K
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...
2.1K
Formation of Muscle Fibers from Myoblasts01:13

Formation of Muscle Fibers from Myoblasts

5.3K
De novo myogenesis, or the formation of muscle fibers, begins during the early embryonic stages. The skeletal muscle is formed from somites– blocks of embryonic cell layers. The somites are further divided into dermatomes, myotomes, sclerotomes, and syndetomes. Among these, the myotomes give rise to muscle fibers.
Muscle progenitor cells (MPCs) are formed from the myotomes. MPCs express genes that encode the transcription factors Pax3 and Pax7. Along with Pax 3/7, other transcription...
5.3K
mTOR Signaling and Cancer Progression03:03

mTOR Signaling and Cancer Progression

3.9K
The mammalian target of rapamycin or mTOR protein was discovered in 1994 due to its direct interaction with rapamycin. The protein gets its name from a yeast homolog called TOR. The mTOR protein complex in mammalian cells plays a major role in balancing anabolic processes such as the synthesis of proteins, lipids, and nucleotides and catabolic processes, such as autophagy in response to environmental cues, such as availability of nutrients and growth factors.
The mTOR pathway or the...
3.9K
PI3K/mTOR/AKT Signaling Pathway01:22

PI3K/mTOR/AKT Signaling Pathway

4.2K
The mammalian target of rapamycin  (mTOR) is a serine/threonine kinase that regulates growth, proliferation, and cell survival in response to hormones, growth factors, or nutrient availability. This kinase exists in two structurally and functionally distinct forms: mTOR complex 1  (mTORC1) and mTOR complex 2  (mTORC2). The first form (mTORC1) is composed of a rapamycin-sensitive Raptor and proline-rich Akt substrate, PRAS40. In contrast,  mTORC2 consists of a...
4.2K
Mitogens and the Cell Cycle02:38

Mitogens and the Cell Cycle

7.1K
Mitogens and their receptors play a crucial role in controlling the progression of the cell cycle. However, the loss of mitogenic control over cell division leads to tumor formation. Therefore, mitogens and mitogen receptors play an important role in cancer research. For instance, the epidermal growth factor (EGF) - a type of mitogen and its transmembrane receptor (EGFR), decides the fate of the cell's proliferation. When EGF binds to EGFR, a member of the ErbB family of tyrosine kinase...
7.1K

You might also read

Related Articles

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

Sort by
Same journal

A unified catalytic mechanism in bifunctional DNA glycosylases with an evolutionarily conserved aspartate-lysine dyad.

Nature communications·2026
Same journal

Uncovering an alternate pathway of antibiotic resistance in spore-forming bacteria.

Nature communications·2026
Same journal

Efficient Gillespie algorithms for spreading phenomena in large and heterogeneous higher-order networks.

Nature communications·2026
Same journal

ADAPT-M: a workflow for rapid, quantitative in vitro measurements of enriched protein libraries.

Nature communications·2026
Same journal

Local, but not circulating, complement C3 shapes immune checkpoint blockade efficacy by controlling myeloid cell infiltration.

Nature communications·2026
Same journal

Comprehensive benchmarking of tools for nanopore-based detection of DNA methylation.

Nature communications·2026
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: Oct 17, 2025

Single Myofiber Culture Assay for the Assessment of Adult Muscle Stem Cell Functionality Ex Vivo
09:19

Single Myofiber Culture Assay for the Assessment of Adult Muscle Stem Cell Functionality Ex Vivo

Published on: February 15, 2021

5.1K

p107 mediated mitochondrial function controls muscle stem cell proliferative fates.

Debasmita Bhattacharya1,2, Vicky Shah1,3, Oreoluwa Oresajo1,2

  • 1Stem Cell Research Group, York University, Toronto, ON, M3J 1P3, Canada.

Nature Communications
|October 14, 2021
PubMed
Summary

Mitochondrial protein p107 controls myogenic progenitor (MP) proliferation by regulating energy production. Its interaction with Sirt1 influences cell cycle rate, offering insights into muscle aging and disease.

More Related Videos

Improving the Accuracy of Flow Cytometric Assessment of Mitochondrial Membrane Potential in Hematopoietic Stem and Progenitor Cells Through the Inhibition of Efflux Pumps
07:17

Improving the Accuracy of Flow Cytometric Assessment of Mitochondrial Membrane Potential in Hematopoietic Stem and Progenitor Cells Through the Inhibition of Efflux Pumps

Published on: July 30, 2019

8.0K
FACS-Isolation and Culture of Fibro-Adipogenic Progenitors and Muscle Stem Cells from Unperturbed and Injured Mouse Skeletal Muscle
11:25

FACS-Isolation and Culture of Fibro-Adipogenic Progenitors and Muscle Stem Cells from Unperturbed and Injured Mouse Skeletal Muscle

Published on: June 8, 2022

6.5K

Related Experiment Videos

Last Updated: Oct 17, 2025

Single Myofiber Culture Assay for the Assessment of Adult Muscle Stem Cell Functionality Ex Vivo
09:19

Single Myofiber Culture Assay for the Assessment of Adult Muscle Stem Cell Functionality Ex Vivo

Published on: February 15, 2021

5.1K
Improving the Accuracy of Flow Cytometric Assessment of Mitochondrial Membrane Potential in Hematopoietic Stem and Progenitor Cells Through the Inhibition of Efflux Pumps
07:17

Improving the Accuracy of Flow Cytometric Assessment of Mitochondrial Membrane Potential in Hematopoietic Stem and Progenitor Cells Through the Inhibition of Efflux Pumps

Published on: July 30, 2019

8.0K
FACS-Isolation and Culture of Fibro-Adipogenic Progenitors and Muscle Stem Cells from Unperturbed and Injured Mouse Skeletal Muscle
11:25

FACS-Isolation and Culture of Fibro-Adipogenic Progenitors and Muscle Stem Cells from Unperturbed and Injured Mouse Skeletal Muscle

Published on: June 8, 2022

6.5K

Area of Science:

  • Cellular metabolism
  • Mitochondrial biology
  • Stem cell research

Background:

  • Muscle diseases and aging impair myogenic stem cell self-renewal and progenitor proliferation.
  • Distinct metabolic states (glycolysis vs. oxidative phosphorylation) influence progenitor cell behavior.
  • The interplay between these metabolic pathways in progenitor cells is not fully understood.

Purpose of the Study:

  • To elucidate the mechanism by which mitochondrial-localized transcriptional co-repressor p107 regulates myogenic progenitor (MP) proliferation.
  • To investigate the role of p107 in controlling cellular energy metabolism and its impact on cell cycle progression.

Main Methods:

  • Investigated the interaction of p107 with mitochondrial DNA.
  • Assessed the effect of p107 on mitochondrial-encoded gene transcription and ATP production.
  • Examined the relationship between p107's mitochondrial function, ATP output, and cell cycle rate.
  • Studied the interaction between Sirt1 activity and p107 localization.

Main Results:

  • p107 directly interacts with mitochondrial DNA, repressing mitochondrial gene transcription and reducing ATP production.
  • Reduced ATP output, controlled by p107's mitochondrial function, correlates with slower cell cycle rates.
  • Sirt1 activity impedes p107's mitochondrial localization by interacting with it.

Conclusions:

  • Mitochondrial p107 function is a key regulator of MP proliferation through metabolic control.
  • The p107-Sirt1 interaction modulates cellular energy balance and cell cycle progression.
  • This mechanism provides a new paradigm for understanding cell cycle regulation in dividing cells, potentially relevant to aging and muscle disease.