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

Assembly of Complex Microtubule Structures01:32

Assembly of Complex Microtubule Structures

2.4K
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.
2.4K
Spindle Assembly02:50

Spindle Assembly

4.2K
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...
4.2K
Centrioles and Centrosomes01:13

Centrioles and Centrosomes

5.4K
Most animal cells comprise a pair of centrioles together called a centrosome. The cell duplicates its centrosome and contains two centrosomes side-by-side, which begin to move apart during the prophase. As the centrosomes migrate to two different sides of the cell, microtubules start extending from each centrosome toward the other end. The mitotic spindle is composed of the centrosomes and their emerging microtubules.
Near the end of the prophase, also called late prophase or...
5.4K
Microtubule Formation01:23

Microtubule Formation

7.4K
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...
7.4K
Microtubules in Cell Motility01:24

Microtubules in Cell Motility

4.5K
Microtubules are thick hollow cylindrical proteins that help form the cytoskeleton. Microtubules have varied roles in the cell. These filaments help form cellular appendages like cilia and flagella, which are responsible for locomotion. The cilia arise from basal bodies, separated from the main body by a membrane-like structure forming the transition zone. This zone is the gate for the entry of lipids and proteins, creating a unique composition of lipids and proteins in the ciliary membrane and...
4.5K
Microtubule Associated Motor Proteins01:32

Microtubule Associated Motor Proteins

10.3K
Eukaryotic cells have different motor proteins for transporting various cargo within the cell. These motor proteins differ based on the filament they associate with, the direction they move within the cell, and the type of cargo they transport. Motor proteins that associate with microtubules are known as microtubule-associated motor proteins. There are two families of microtubule-associated motor proteins —Kinesins and Dyneins. Both these proteins assist in the transport of cellular...
10.3K

You might also read

Related Articles

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

Sort by
Same author

Targeted glycophagy ATG8 therapy reverses diabetic heart disease in mice and in human engineered cardiac tissues.

bioRxiv : the preprint server for biology·2025
Same author

Targeted glycophagy ATG8 therapy reverses diabetic heart disease in mice and in human engineered cardiac tissues.

Nature cardiovascular research·2025
Same author

Catch me if you can: targeting the mitochondrial permeability transition pore in myocardial infarction.

Cell death and differentiation·2015
Same author

A novel role for the apoptosis inhibitor ARC in suppressing TNFα-induced regulated necrosis.

Cell death and differentiation·2014
Same author

Kinetics of the translocation and phosphorylation of alphaB-crystallin in mouse heart mitochondria during ex vivo ischemia.

American journal of physiology. Heart and circulatory physiology·2009
Same author

Localization of phosphorylated alphaB-crystallin to heart mitochondria during ischemia-reperfusion.

American journal of physiology. Heart and circulatory physiology·2007

Related Experiment Video

Updated: Jan 17, 2026

Assembly of Complex Microtubule Structures
01:32

Assembly of Complex Microtubule Structures

2.4K

Seeing death in the living

R A Gottlieb, R N Kitsis

    Nature Medicine
    |December 1, 2001
    PubMed
    Summary

    No abstract available in PubMed .

    More Related Videos

    Spindle assembly: Dynein, Kinesin and Microtubules
    02:50

    Spindle assembly: Dynein, Kinesin and Microtubules

    4.2K
    Centrioles and Centrosomes
    01:13

    Centrioles and Centrosomes

    5.4K

    Related Experiment Videos

    Last Updated: Jan 17, 2026

    Assembly of Complex Microtubule Structures
    01:32

    Assembly of Complex Microtubule Structures

    2.4K
    Spindle assembly: Dynein, Kinesin and Microtubules
    02:50

    Spindle assembly: Dynein, Kinesin and Microtubules

    4.2K
    Centrioles and Centrosomes
    01:13

    Centrioles and Centrosomes

    5.4K