Dual spatio-temporal regulation of axon growth and microtubule dynamics by RhoA signaling pathways

Author:

Wojnacki José1ORCID,Quassollo Gonzalo1ORCID,Bordenave Martín D.2,Unsain Nicolás13ORCID,Martínez Gaby F.1,Szalai Alan M.2ORCID,Pertz Olivier4ORCID,Gundersen Gregg G.5ORCID,Bartolini Francesca5ORCID,Stefani Fernando D.26ORCID,Cáceres Alfredo7ORCID,Bisbal Mariano13ORCID

Affiliation:

1. Instituto de Investigación Médica Mercedes y Martín Ferreyra (INIMEC), Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Universidad Nacional de Córdoba 1 , Córdoba 5016 , Argentina

2. Centro de Investigaciones en Bionanociencias (CIBION), Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET) 2 , Godoy Cruz 2390, Ciudad Autónoma de Buenos Aires C1425FQD , Argentina

3. Instituto Universitario Ciencias Biomédicas de Córdoba (IUCBC) 3 , Córdoba 5016 , Argentina

4. Institute of Cell Biology, University of Bern 4 , Baltzerstrasse 4, Bern 3012 , Switzerland

5. Vagelos College of Physicians and Surgeons, Columbia University 5 Department of Pathology and Cell Biology , , New York, NY 10032 , USA

6. Universidad de Buenos Aires 6 Departamento de Física, Facultad de Ciencias Exactas y Naturales , , Güiraldes 2620, Ciudad Autónoma de Buenos Aires C1428EHA , Argentina

7. Centro Investigación Medicina Traslacional Severo R Amuchástegui (CIMETSA), Instituto Universitario Ciencias Biomédicas Córdoba (IUCBC) 7 , Av. Naciones Unidas 440, Córdoba 5016 , Argentina

Abstract

ABSTRACT RhoA plays a crucial role in neuronal polarization, where its action restraining axon outgrowth has been thoroughly studied. We now report that RhoA has not only an inhibitory but also a stimulatory effect on axon development depending on when and where exerts its action and the downstream effectors involved. In cultured hippocampal neurons, FRET imaging revealed that RhoA activity selectively localized in growth cones of undifferentiated neurites, whereas in developing axons it displayed a biphasic pattern, being low in nascent axons and high in elongating ones. RhoA–Rho kinase (ROCK) signaling prevented axon initiation but had no effect on elongation, whereas formin inhibition reduced axon extension without significantly altering initial outgrowth. In addition, RhoA–mDia signaling promoted axon elongation by stimulating growth cone microtubule stability and assembly, as opposed to RhoA–ROCK signaling, which restrained growth cone microtubule assembly and protrusion.

Funder

Agencia Nacional de Promoción Científica y Tecnológica

International Brain Research Organization

Alzheimer's Association

National Council on Scientific and Technical Research

Publisher

The Company of Biologists

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