Why the study?
Does siRNA knockdown of Myosin VI affect cell migration, proliferation, and catecholamine secretion in PC12 cells?
Does siRNA knockdown of Myosin VI affect cell migration, proliferation, and catecholamine secretion in PC12 cells?
In PC12 cells, Myosin VI is essential for cell migration, proliferation, and cytoskeleton/Golgi organization, but is not crucial for catecholamine release.
MVI dispensable for noradrenaline secretion in PC12 cells; leaves open its targeting for migration/proliferation disorders.
Myosin VI (MVI) is the only known myosin walking towards minus end of actin filaments and is believed to play distinct role(s) than other myosins. We addressed a role of this unique motor in secretory PC12 cells, derived from rat adrenal medulla pheochromocytoma using cell lines with reduced MVI synthesis (produced by means of siRNA). Decrease of MVI expression caused severe changes in cell size and morphology, and profound defects in actin cytoskeleton organization and Golgi structure. Also, significant inhibition of cell migration as well as cell proliferation was observed. Flow cytometric analysis revealed that MVI-deficient cells were arrested in G0/G1 phase of the cell cycle but did not undergo increased senescence as compared with control cells. Also, neither polyploidy nor aneuploidy were detected. Surprisingly, no significant effect on noradrenaline secretion was observed. These data indicate that in PC12 cells MVI is involved in cell migration and proliferation but is not crucial for stimulation-dependent catecholamine release.
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Majewski et al. (2011) studied this question.
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