Regulation of axon growth by myosin II–dependent mechanocatalysis of cofilin activity

Author:

Zhang Xiao-Feng1ORCID,Ajeti Visar12,Tsai Nicole13,Fereydooni Arash1ORCID,Burns William1,Murrell Michael4,De La Cruz Enrique M.5,Forscher Paul1ORCID

Affiliation:

1. Department of Molecular, Cellular and Developmental Biology, Yale University, New Haven, CT

2. Department of Biomedical Engineering, University of Connecticut Health Center, Farmington, CT

3. Department of Ophthalmology, University of California, San Francisco, California, CA

4. Department of Biomedical Engineering, Yale University, New Haven, CT

5. Department of Molecular Biophysics and Biochemistry, Yale University, New Haven, CT

Abstract

Serotonin (5-HT) is known to increase the rate of growth cone advance via cofilin-dependent increases in retrograde actin network flow and nonmuscle myosin II activity. We report that myosin II activity is regulated by PKC during 5-HT responses and that PKC activity is necessary for increases in traction force normally associated with these growth responses. 5-HT simultaneously induces cofilin-dependent decreases in actin network density and PKC-dependent increases in point contact density. These reciprocal effects facilitate increases in traction force production in domains exhibiting decreased actin network density. Interestingly, when PKC activity was up-regulated, 5-HT treatments resulted in myosin II hyperactivation accompanied by catastrophic cofilin-dependent decreases in actin filament density, sudden decreases in traction force, and neurite retraction. These results reveal a synergistic relationship between cofilin and myosin II that is spatiotemporally regulated in the growth cone via mechanocatalytic effects to modulate neurite growth.

Funder

National Institutes of Health

U.S. Department of Defense

Army Research Office

Publisher

Rockefeller University Press

Subject

Cell Biology

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