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

Role of Microtubules in Cell Wall Deposition01:02

Role of Microtubules in Cell Wall Deposition

2.5K
Microtubules are small hollow tubes in eukaryotic cells. The cell wall microtubules are polymerized dimers of two globular proteins, α-tubulin and β-tubulin, two globular proteins. With a diameter of about 25 nm, microtubules are the widest components of the cytoskeleton. They help the cell resist compression and provide a track along which vesicles move through the cell or pull replicated chromosomes to opposite ends of a dividing cell. Microtubules go through quick cycles of...
2.5K
Assembly of Complex Microtubule Structures01:32

Assembly of Complex Microtubule Structures

1.9K
Complex microtubule structures are present in resting cells and in dividing cells. In resting cells, they are responsible for maintaining the cellular architecture, tracks for intracellular transport, positioning of organelles, assembly of cilia and flagella. They mediate the bipolar spindle assembly for chromosomal segregation and positioning of the cell division plate in dividing cells. The formation of microtubule complex structures depends on the cell type, cell stage, and cell function.
1.9K
Microtubule Formation01:23

Microtubule Formation

5.9K
Microtubules are dynamic structures that undergo continuous assembly and disassembly. They originate from specialized multi-protein complexes known as microtubule organizing centers or MTOCs. Within the MTOC, the point of origin of the microtubule is known as the minus end, while the end radiating outward is the plus end. Microtubules serve two primary functions — the organization of spindle complexes to separate sister chromatids during mitotic or meiotic cell division and the formation...
5.9K
Spindle Assembly02:50

Spindle Assembly

3.7K
Spindle assembly occurs through three, often coexisting, pathways – the centrosome-mediated pathway, the chromatin-mediated pathway, and the microtubule-mediated pathway – collectively contributing to form a robust spindle apparatus.
In most cells, centrosomes are the primary microtubule nucleation centers. In the centrosome-mediated pathway, the G2-prophase transition triggers centrosome maturation and increased microtubule nucleation. Progressive nucleation results in a...
3.7K
Microtubules01:35

Microtubules

87.8K
There are three types of cytoskeletal structures in eukaryotic cells—microfilaments, intermediate filaments, and microtubules. With a diameter of about 25 nm, microtubules are the thickest of these fibers. Microtubules carry out a variety of functions that include cell structure and support, transport of organelles, cell motility (movement), and the separation of chromosomes during cell division.
87.8K
Microtubule Instability02:17

Microtubule Instability

5.2K
Microtubules are hollow cylindrical filaments having a diameter of approximately 25 nm and a length that varies from 200 nm to 25 μm. GTP-bound tubulin subunits form αβ-heterodimers for microtubule assembly. These core building blocks interact longitudinally, polymerizing into protofilaments. The protofilaments then interact with one another through lateral bonding forces to form stable cylindrical microtubules. These cylindrical filaments are dynamic as they undergo repeated...
5.2K

You might also read

Related Articles

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

Sort by
Same author

Self-assembly: From blueprints to breakthroughs.

The Journal of chemical physics·2026
Same author

Vacancy defects in square-triangle tilings and their implications for quasicrystals formed by square-shoulder particles.

The Journal of chemical physics·2026
Same author

Determining fluid-crystal phase boundaries for a binary hard-sphere mixture using direct-coexistence simulations.

The Journal of chemical physics·2026
Same author

Solid-angle based nearest-neighbor algorithm adapted for systems with low coordination number.

The Journal of chemical physics·2026
Same author

Quantitative 3D Real-Space Analysis of Photonic Supraparticles.

Advanced materials (Deerfield Beach, Fla.)·2026
Same author

Comparing dimensionality reduction methods for local structural identification in colloidal systems.

The Journal of chemical physics·2026

Related Experiment Video

Updated: Aug 18, 2025

Self-Assembly of Microtubule Tactoids
08:49

Self-Assembly of Microtubule Tactoids

Published on: June 23, 2022

4.0K

Microtubule nucleation complex behavior is critical for cortical array homogeneity and xylem wall patterning.

Bas Jacobs1, René Schneider2, Jaap Molenaar1

  • 1Mathematical and Statistical Methods (Biometris), Plant Science Group, Wageningen University, 6708 PB Wageningen, the Netherlands.

Proceedings of the National Academy of Sciences of the United States of America
|December 8, 2022
PubMed
Summary

Plant cells balance microtubule nucleation to ensure uniform cell walls. A novel mechanism involving nucleation complex recruitment prevents pattern defects, enabling diverse mechanical properties for plant growth.

Keywords:
homogeneitynucleationplant cortical microtubulesstable coexistencestochastic simulation

More Related Videos

Live Cell Imaging of Microtubule Cytoskeleton and Micromechanical Manipulation of the Arabidopsis Shoot Apical Meristem
07:52

Live Cell Imaging of Microtubule Cytoskeleton and Micromechanical Manipulation of the Arabidopsis Shoot Apical Meristem

Published on: May 23, 2020

5.4K
High-resolution Time-lapse Imaging and Automated Analysis of Microtubule Dynamics in Living Human Umbilical Vein Endothelial Cells
10:25

High-resolution Time-lapse Imaging and Automated Analysis of Microtubule Dynamics in Living Human Umbilical Vein Endothelial Cells

Published on: August 13, 2016

11.2K

Related Experiment Videos

Last Updated: Aug 18, 2025

Self-Assembly of Microtubule Tactoids
08:49

Self-Assembly of Microtubule Tactoids

Published on: June 23, 2022

4.0K
Live Cell Imaging of Microtubule Cytoskeleton and Micromechanical Manipulation of the Arabidopsis Shoot Apical Meristem
07:52

Live Cell Imaging of Microtubule Cytoskeleton and Micromechanical Manipulation of the Arabidopsis Shoot Apical Meristem

Published on: May 23, 2020

5.4K
High-resolution Time-lapse Imaging and Automated Analysis of Microtubule Dynamics in Living Human Umbilical Vein Endothelial Cells
10:25

High-resolution Time-lapse Imaging and Automated Analysis of Microtubule Dynamics in Living Human Umbilical Vein Endothelial Cells

Published on: August 13, 2016

11.2K

Area of Science:

  • Plant Biology
  • Cell Biology
  • Biophysics

Background:

  • Plant cell wall mechanics are crucial for integrity and function.
  • Cellulose fibril distribution, guided by cortical microtubules, dictates mechanical properties.
  • Microtubule nucleation dynamics can lead to pattern inhomogeneity, posing a challenge for uniform cell wall formation.

Purpose of the Study:

  • To identify the mechanism balancing microtubule nucleation for homogeneous cell wall patterns.
  • To investigate the role of nucleation complex recruitment versus tubulin depletion.
  • To understand how microtubule dynamics influence fibril patterning in specialized cells like protoxylem.

Main Methods:

  • Combined experimental observations with stochastic simulations.
  • Investigated nucleation complex localization at the plasma membrane.
  • Modeled the effect of nucleation complex recruitment on microtubule array dynamics.

Main Results:

  • Limited local recruitment of nucleation complexes to microtubules effectively counters positive feedback.
  • Local tubulin depletion does not prevent microtubule array inhomogeneity.
  • Nucleation complexes show preferential localization near microtubules at the plasma membrane.
  • Simulations incorporating experimental findings demonstrate a balance mechanism that allows rapid pattern changes.

Conclusions:

  • A novel balancing mechanism involving nucleation complex recruitment regulates microtubule organization.
  • This mechanism prevents excessive inhomogeneity, ensuring functional cell walls.
  • The system allows for dynamic pattern adaptation, as seen in protoxylem development.
  • Findings enhance the predictive power of computational models in cell biology.