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Related Concept Videos

Destabilization of Microtubules01:45

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The destabilization of microtubules can occur during different stages of the microtubule lifecycle, such as nucleation or elongation. It can take place at either end of the microtubule or in the microtubule lattices as a whole. The lifespan of individual microtubules within a cell varies according to the cell type and stage of the cell cycle. During interphase, the lifespan of the microtubule is about 30 minutes, while during cell division, it is about 15 minutes. In axonal microtubules of...
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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...
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Microtubules form through the end-to-end polymerization of tubulin heterodimers. Kinetochore microtubules originate from the spindle poles, and their plus-ends connect with the kinetochores on sister-chromatids. Ndc80 protein complexes, present on the kinetochore, form low-affinity links with the plus end of these kinetochore microtubules.
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Related Experiment Video

Updated: May 3, 2026

Measurement of Microtubule Dynamics by Spinning Disk Microscopy in Monopolar Mitotic Spindles
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A new directionality tool for assessing microtubule pattern alterations.

Wenhua Liu1, Evelyn Ralston

  • 1Light Imaging Section, Office of Science and Technology, National Institute of Arthritis and Musculoskeletal and Skin Diseases, National Institutes of Health, Bethesda, Maryland.

Cytoskeleton (Hoboken, N.J.)
|February 6, 2014
PubMed
Summary
This summary is machine-generated.

A new software tool, texture detection technique (TeDT), quantifies microtubule directionality in muscle fibers. This method aids in understanding muscle diseases like Duchenne muscular dystrophy (DMD) by providing objective data.

Keywords:
Duchenne muscular dystrophydirectionalitygray-level co-occurrence matricesmicrotubulemuscle fibertexture correlation

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Area of Science:

  • Cell Biology
  • Biophysics
  • Biomedical Engineering

Background:

  • The cytoskeleton, including microtubules, exhibits cell type-specific organization crucial for cell health.
  • Alterations in microtubule organization are implicated in muscle diseases such as Duchenne muscular dystrophy (DMD).
  • Current visual assessment of microtubule patterns is subjective and lacks quantitative accuracy, especially in complex fiber types.

Purpose of the Study:

  • To develop a robust software program for detecting and quantifying microtubule directionality.
  • To overcome limitations of existing methods that focus on local image features.
  • To provide a quantitative tool for assessing microtubule organization in various muscle fiber types and disease models.

Main Methods:

  • Development of a texture detection technique (TeDT) based on the Haralick texture method.
  • TeDT incorporates both local and global image features, emphasizing global characteristics.
  • The software generates graphical representations and numerical scores for microtubule directionality.

Main Results:

  • TeDT successfully quantifies microtubule directionality in fast-twitch muscle fibers of wild-type and mdx mice (a DMD model).
  • The tool accurately assesses microtubule directionality in slow-twitch fibers and in young animals, which were previously difficult to evaluate visually.
  • Results are independent of imaging conditions and post-imaging procedures, ensuring robustness.

Conclusions:

  • TeDT provides a reliable and quantitative method for assessing microtubule directionality across different muscle fiber types.
  • This tool can significantly aid research into muscle diseases like DMD by offering objective data on cytoskeletal organization.
  • TeDT holds potential for assessing the directionality of other cytoskeletal components as well.