“…However, our results contrast with recent data that show that inhibition of formins increases the half time of actin turnover in other cell types, including M2 melanoma cells, neurons, vascular cells and fibroblasts (Fritzsche et al, 2013;Ganguly et al, 2015; Phng et al, 2015;Sahasrabudhe et al, 2016). Clearly, however, the functions of formin proteins differ between cell types and actin populations, because loss of formins decreased the mobile actin fractions in fibroblasts and neurons (Ganguly et al, 2015;Sahasrabudhe et al, 2016) yet left the mobile fraction unchanged in vascular cells (Phng et al, 2015), similar to the case here for MCCs. Moreover, in systems in which an actin network forms de novo, such as in the cortex of retracting blebs, actin turnover is almost tenfold higher compared with that in the mature cortex, suggesting that the molecular mechanisms regulating actin turnover in new cortices are different compared to those in mature networks (Bovellan et al, 2014).…”