Movement of the actin filament bundle in Mytilus sperm: a new mechanism is proposed
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Abstract:
An actin filament bundle approximately 2-5 microns in length is present in the sperm of the blue mussel, Mytilus. In unfired sperm this bundle extends from the midpiece through a canal in the center of the nucleus to terminate on the membrane limiting the inside of the cone-shaped acrosomal vacuole. The bundle is composed of 45-65 actin filaments which are hexagonally packed and regularly cross-bridged together to form an actin paracrystal so well ordered that it has six nearly equal faces. Upon induction of the acrosomal reaction, a needle-like process is formed in a few seconds. Within this process is the actin filament bundle which appears unchanged in filament number and packing as determined by optical diffraction methods. Using fluorescein-conjugated phalloidin we were able to establish that the bundle does not change length but instead is projected anteriorly out of the midpiece and nuclear canal like an arrow. Existing mechanisms to explain this extension cannot apply. Specifically, the bundle does not increase in length (no polymerization), does not change its organization (no change in actin twist), does not change filament number (no filament sliding), and cannot move by myosin (wrong polarity). Thus we are forced to look elsewhere for a mechanism and have postulated that at least a component of this movement, or cell elongation, is the interaction of the actin filament bundle with the plasma membrane.
Insights
Mussel sperm actin bundles project like arrows during acrosomal reactions. This actin paracrystal extends without polymerization or sliding, suggesting novel plasma membrane interactions drive sperm elongation.
Area of Science:
- Cell Biology
- Biophysics
- Sperm Motility
Background:
- Mytilus sperm possess a unique actin filament bundle within the acrosomal vacuole.
- This bundle is highly ordered, forming a paracrystal with hexagonal packing.
Purpose of the Study:
- To investigate the mechanism of actin bundle extension during the acrosomal reaction in Mytilus sperm.
- To determine if known actin dynamics mechanisms explain the observed projection.
Main Methods:
- Optical diffraction analysis to assess actin bundle organization.
- Fluorescein-conjugated phalloidin staining to track actin bundle localization and length.
Main Results:
- The actin filament bundle remains unchanged in length, filament number, and organization during acrosomal reaction.
- The bundle is projected anteriorly, extending out of the sperm midpiece and nuclear canal.
- Established mechanisms like polymerization, filament sliding, or myosin motor activity do not explain the movement.
Conclusions:
- The projection of the actin bundle is not due to polymerization or sliding.
- A novel mechanism involving the interaction of the actin bundle with the plasma membrane is proposed.
- This interaction is hypothesized to drive sperm elongation during the acrosomal reaction.