Jove
Visualize
Contact Us
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 Concept Videos

Necrosis01:16

Necrosis

6.3K
Necrosis is considered as an “accidental” or unexpected form of cell death that ends in cell lysis. The first noticeable mention of “necrosis” was in 1859 when Rudolf Virchow used this term to describe advanced tissue breakdown in his compilation titled “Cell Pathology”.
Morphological Manifestations of Necrosis
Necrotic cells show different types of morphological appearance depending on the type of tissue and infection. In coagulative necrosis, cells become...
6.3K
Cells Coordinate Growth and Proliferation02:36

Cells Coordinate Growth and Proliferation

5.0K
Cell size is a significant factor impacting cellular design, function, and fitness. There exists some internal coordination by which cells double their masses before division, thus, achieving homeostasis. Coordination between cell growth and proliferation depends on the checkpoints in between cell cycle phases. Loss of coordination or failure in the checkpoint mechanism can drive the cell to uncontrolled growth and loss of cellular function. Like dividing cells that coordinate cellular growth,...
5.0K

You might also read

Related Articles

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

Sort by
Same author

Cell size modulates ferroptosis susceptibility.

eLife·2026
Same author

The FAM53C/DYRK1A axis regulates the G1/S transition of the cell cycle.

eLife·2026
Same author

Chromatin association promotes UBR5-mediated degradation of Rb.

bioRxiv : the preprint server for biology·2026
Same author

Dissecting Complex Interactions Between Ferroptosis and the Proteasome.

bioRxiv : the preprint server for biology·2026
Same author

Identification and inhibition of the Cyclin D Rb-docking interface that drives cell division.

bioRxiv : the preprint server for biology·2026
Same author

Emerging Strategies to Inhibit the G1/S Transition for Cancer Therapy.

Cancer research·2026
Same journal

Layered social competition coordinates reproductive hierarchy formation in ants.

bioRxiv : the preprint server for biology·2026
Same journal

Combination epigenetic-targeted therapy increases the immunogenicity of poorly immunogenic sarcomas.

bioRxiv : the preprint server for biology·2026
Same journal

Loss of LanC-like proteins delays post-injury regeneration of aging skeletal muscles.

bioRxiv : the preprint server for biology·2026
Same journal

Integrative Transfer Network: Deep Transfer Learning Across Populations and Prediction Targets.

bioRxiv : the preprint server for biology·2026
Same journal

Confidence-supported label-free metabolic imaging with FPhaS phase autofluorescence microscopy.

bioRxiv : the preprint server for biology·2026
Same journal

Sequence-encoded autoinhibition couples mRNA decapping activity to phase separation.

bioRxiv : the preprint server for biology·2026
See all related articles

Related Experiment Video

Updated: Jan 10, 2026

Author Spotlight: Tracing the Ferroptotic Signatures and Cell Death Dynamics in Medulloblastoma for Advanced Therapeutics
04:01

Author Spotlight: Tracing the Ferroptotic Signatures and Cell Death Dynamics in Medulloblastoma for Advanced Therapeutics

Published on: March 15, 2024

1.8K

Cell size modulates ferroptosis susceptibility.

Evgeny Zatulovskiy1,2, Magdalena B Murray2, Shuyuan Zhang2

  • 1Department of Biochemistry, University of Cambridge, Cambridge, CB2 1GA, UK.

Biorxiv : the Preprint Server for Biology
|November 24, 2025
PubMed
Summary
This summary is machine-generated.

Cell size significantly impacts cell death resistance. Larger cells are more resistant to ferroptosis, a cell death pathway, due to higher glutathione levels and lower lipid peroxidation.

More Related Videos

Ferritinophagy: Assessing the Selective Degradation of Iron by Autophagy in Human Fibroblasts
09:21

Ferritinophagy: Assessing the Selective Degradation of Iron by Autophagy in Human Fibroblasts

Published on: February 23, 2024

1.4K

Related Experiment Videos

Last Updated: Jan 10, 2026

Author Spotlight: Tracing the Ferroptotic Signatures and Cell Death Dynamics in Medulloblastoma for Advanced Therapeutics
04:01

Author Spotlight: Tracing the Ferroptotic Signatures and Cell Death Dynamics in Medulloblastoma for Advanced Therapeutics

Published on: March 15, 2024

1.8K
Ferritinophagy: Assessing the Selective Degradation of Iron by Autophagy in Human Fibroblasts
09:21

Ferritinophagy: Assessing the Selective Degradation of Iron by Autophagy in Human Fibroblasts

Published on: February 23, 2024

1.4K

Area of Science:

  • Cell Biology
  • Biochemistry
  • Physiology

Background:

  • Cell size is a fundamental property influencing cellular physiology and proteome composition.
  • Differences in biochemical composition between large and small cells suggest varying responses to signals.

Purpose of the Study:

  • To investigate the impact of cell size on susceptibility to cell death.
  • To determine if cell size affects ferroptosis, an iron-dependent cell death pathway.

Main Methods:

  • Comparison of large and small cells regarding ferroptosis induction.
  • Quantification of glutathione, lipid peroxides, ACSL4, ferritin, glutamate-cysteine ligase, and glutathione synthetase concentrations.

Main Results:

  • Larger cells demonstrated increased resistance to ferroptosis induced by system xc- inhibition.
  • Larger cells exhibited higher glutathione concentrations and lower membrane lipid peroxides.
  • Mechanisms included lower ACSL4, higher ferritin, and increased glutathione-synthesizing enzymes in larger cells.

Conclusions:

  • Cell size significantly influences cellular function and survival.
  • A size-dependent vulnerability to ferroptosis was identified.
  • Findings may impact therapeutic strategies targeting ferroptosis.