Video 9.

Segments of dendrite (left, middle) or dendrite growth cone (right) from live primary cortical neurons derived from wild-type (WT) or EVL knockout (KO) mice at day in vitro 11 (D11) expressing mRuby2-LifeAct. Cultures were treated with 0.1% DMSO, 100 µM CK-666, or 50 µM Blebbistatin at 5 min, and imaged for 40 min following treatment (treatment period indicated by yellow square). Growth cone dynamics were monitored as a read-out for approximating the time to maximal inhibition of Arp2/3 (∼20 min) and myosin activity (∼15 min) in neurons. Scale bar = 10 µm. 15 s interval, 45 min duration, 10 fps. See also Fig. 8.


EVL and MIM/MTSS1 regulate actin cytoskeletal remodeling to promote dendritic filopodia in neurons

Sara S. Parker, Kenneth Tran Ly, Adam D. Grant, Jillian Sweetland, Ashley M. Wang, James D. Parker, Mackenzie R. Roman, Kathylynn Saboda, Denise J. Roe, Megha Padi, Charles W. Wolgemuth, Paul Langlais, and Ghassan Mouneimne

DOI: 10.1083/jcb.202106081
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