Key result
Reducing the expression of MyH7B in mature neurons caused profound alterations to dendritic spine structure and significantly reduced miniature EPSC amplitudes (9.8 pA vs 13.28 pA, p<0.01).
The discovery and characterization of the MyH7B myosin II isoform in neurons reveals a novel regulatory mechanism for actin dynamics, dendritic spine morphology, and excitatory synaptic strength.
Extends myosin II's role in synaptic structure to mature neurons in animals; leaves open relevance to human neurological disorders pending validation.
Ongoing synaptic function and rapid, bidirectional plasticity are both controlled by regulatory mechanisms within dendritic spines. Spine actin dynamics maintain synapse structure and function, and cytoskeletal rearrangements in these structures trigger structural and functional plasticity. Therefore, proteins that interact with actin filaments are attractive candidates to regulate synaptic actin dynamics and, thus, synapse structure and function. Here, we have cloned the rat isoform of class II myosin heavy chain MyH7B in brain. Unexpectedly, this isoform resembles muscle-type myosin II rather than the ubiquitously expressed nonmuscle myosin II isoforms, suggesting that a rich functional diversity of myosin II motors may exist in neurons. Indeed, reducing the expression of MyH7B in mature neurons caused profound alterations to dendritic spine structure and excitatory synaptic strength. Structurally, dendritic spines had large, irregularly shaped heads that contained many filopodia-like protrusions. Neurons with reduced MyH7B expression also had impaired miniature EPSC amplitudes accompanied by a decrease in synaptic AMPA receptors, which was linked to alterations of the actin cytoskeleton. MyH7B-mediated control over spine morphology and synaptic strength was distinct from that of a nonmuscle myosin, myosin IIb. Interestingly, when myosin IIb expression and MyH7B expression were simultaneously knocked-down in neurons, a third, more pronounced phenotype emerged. Together, our data provide evidence that distinct myosin II isoforms work together to regulate synapse structure and function in cultured hippocampal neurons. Thus, myosin II motor activity is emerging as a broad regulatory mechanism for control over complex actin networks within dendritic spines.
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Rubio et al. (2011) studied this question. MyH7B knockdown (siRNA) vs. Control siRNA was evaluated on miniature EPSC amplitude (p=<0.01). Reducing the expression of MyH7B in mature neurons caused profound alterations to dendritic spine structure and significantly reduced miniature EPSC amplitudes (9.8 pA vs 13.28 pA, p<0.01).
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