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Updated: Aug 18, 2026

Computational Analysis of the Caenorhabditis elegans Germline to Study the Distribution of Nuclei, Proteins, and the Cytoskeleton
Published on: April 19, 2018
A unique cytoskeleton associated with crawling in the amoeboid sperm of the nematode, Ascaris suum
S Sepsenwol1, H Ris, T M Roberts
1Department of Biology, University of Wisconsin-Stevens Point 54481.
Abstract:
Nematode sperm extend pseudopods and pull themselves over substrates. They lack an axoneme or the actin and myosins of other types of motile cells, but their pseudopods contain abundant major sperm protein (MSP), a family of 14-kD polypeptides found exclusively in male gametes. Using high voltage electron microscopy, a unique cytoskeleton was discovered in the pseudopod of in vitro-activated, crawling sperm of the pig intestinal nematode Ascaris suum. It consists of 5-10-nm fuzzy fibers organized into 150-250-nm-thick fiber complexes, which connect to each of the moving pseudopodial membrane projections, villipodia, which in turn make contact with the substrate. Individual fibers in a complex splay out radially from its axis in all directions. The centripetal ends intercalate with fibers from other complexes or terminate in a thickened layer just beneath the pseudopod membrane. Monoclonal antibodies directed against MSP heavily label the fiber complexes as well as individual pseudopodial filaments throughout their length. This represents the first evidence that MSP may be the major filament protein in the Ascaris sperm cytoskeleton. The large fiber complexes can be seen clearly in the pseudopods of live, crawling sperm by computer-enhanced video, differential-interference contrast microscopy, forming with the villipodia at the leading edge of the sperm pseudopod. Even before the pseudopod attaches, the entire cytoskeleton and villipodia move continuously rearwards in unison toward the cell body. During crawling, complexes and villipodia in the pseudopod recede at the same speed as the spermatozoon moves forward, both disappearing at the pseudopod-cell body junction. Sections at this region of high membrane turnover reveal a band of densely packed smooth vesicles with round and tubular profiles, some of which are associated with the pseudopod plasma membrane. The exceptional anatomy, biochemistry, and phenomenology of Ascaris sperm locomotion permit direct study of the involvement of the cytoskeleton in amoeboid motility.
Insights
Ascaris suum nematode sperm use a unique cytoskeleton made of major sperm protein (MSP) fibers for crawling motility. This MSP-based structure propels sperm movement without typical cellular machinery.
Area of Science:
- Cell Biology
- Nematology
- Biochemistry
Background:
- Nematode sperm motility differs from other cell types, lacking typical actin-myosin structures.
- Nematode sperm utilize pseudopods for movement, containing abundant major sperm protein (MSP).
Purpose of the Study:
- To investigate the unique cytoskeleton involved in Ascaris suum nematode sperm locomotion.
- To determine the role of major sperm protein (MSP) in nematode sperm motility.
Main Methods:
- High voltage electron microscopy to visualize sperm cytoskeleton.
- Monoclonal antibodies against MSP to identify protein localization.
- Computer-enhanced video and differential-interference contrast microscopy for live cell observation.
Main Results:
- A novel cytoskeleton composed of 5-10 nm fuzzy fibers organized into larger complexes was discovered in Ascaris sperm pseudopods.
- Major sperm protein (MSP) was identified as a major component of these fibrous structures and pseudopodial filaments.
- Live sperm exhibited continuous rearward movement of the cytoskeleton and villipodia during pseudopod extension and retraction.
Conclusions:
- The Ascaris sperm cytoskeleton is primarily composed of MSP, representing a unique motility mechanism.
- The observed cytoskeletal dynamics support a model of amoeboid motility driven by MSP-based structures.
- This study provides insights into the fundamental mechanisms of cell motility in specialized gametes.
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