Key result
Nonmuscle myosin-2 isoforms act as central regulatory components of the eukaryotic cytoskeleton, mediating cell migration, adhesion, and cytokinesis through tight spatiotemporal regulation.
This review highlights the central regulatory role of nonmuscle myosin-2 isoforms in cytoskeletal dynamics and their impact on cell physiological functions in health and disease.
May inform cytoskeletal research in cardiovascular cells; leaves open therapeutic translation pending validation.
Members of the nonmuscle myosin-2 (NM-2) family of actin-based molecular motors catalyze the conversion of chemical energy into directed movement and force thereby acting as central regulatory components of the eukaryotic cytoskeleton. By cyclically interacting with adenosine triphosphate and F-actin, NM-2 isoforms promote cytoskeletal force generation in established cellular processes like cell migration, shape changes, adhesion dynamics, endo- and exo-cytosis, and cytokinesis. Novel functions of the NM-2 family members in autophagy and viral infection are emerging, making NM-2 isoforms regulators of nearly all cellular processes that require the spatiotemporal organization of cytoskeletal scaffolding. Here, we assess current views about the role of NM-2 isoforms in these activities including the tight regulation of NM-2 assembly and activation through phosphorylation and how NM-2-mediated changes in cytoskeletal dynamics and mechanics affect cell physiological functions in health and disease.
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Heissler et al. (2012) reported a review. Nonmuscle myosin-2 was evaluated. Nonmuscle myosin-2 isoforms act as central regulatory components of the eukaryotic cytoskeleton, mediating cell migration, adhesion, and cytokinesis through tight spatiotemporal regulation.
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