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Updated: Aug 2, 2026

In Vitro Polymerization of F-actin on Early Endosomes
Published on: August 28, 2017
Actin filament polymerization regulates gliding motility by apicomplexan parasites
D M Wetzel1, S Håkansson, K Hu
1Department of Molecular Microbiology, Washington University School of Medicine, St. Louis, Missouri 63110, USA.
Toxoplasma gondii motility relies on precisely controlled actin filaments. Stabilizing these filaments with jasplakinolide (JAS) dramatically increased gliding speed but also disrupted normal movement and host cell entry.
Area of Science:
- Parasitology
- Cell Biology
- Biophysics
Background:
- Host cell entry by Toxoplasma gondii is crucial for infection.
- Parasite actin is predominantly monomeric, with limited understanding of filament dynamics.
- The role of actin filaments in parasite motility remains paradoxical.
Purpose of the Study:
- To investigate the role of actin filaments in Toxoplasma gondii motility.
- To understand how actin filament dynamics influence parasite gliding and host cell invasion.
Main Methods:
- Utilized rapid-freeze electron microscopy to visualize actin filaments.
- Employed jasplakinolide (JAS) to stabilize actin filaments in live and fixed parasites.
- Monitored actin distribution using yellow fluorescent protein (YFP)-actin.
- Assessed parasite motility and directionality via videomicroscopy.
Main Results:
- Actin filaments form beneath the plasma membrane during parasite gliding.
- Jasplakinolide (JAS) treatment led to filament redistribution and spiral patterns.
- JAS treatment increased gliding speed threefold, indicating actin filaments are rate-limiting.
- JAS also caused abnormal motility, including reversed direction and disrupted cell entry.
Conclusions:
- Precisely controlled actin filament polymerization is essential for parasite gliding motility.
- Actin filament dynamics dictate the timing, duration, and directionality of movement in Apicomplexa.
- Targeting actin dynamics offers potential strategies for controlling parasite infections.
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