Affiliation:
1. School of Medicine, Shimane University Department of Neural and Muscular Physiology , , 89-1 Enya-cho, Izumo-shi, Shimane 693-8501 , Japan
Abstract
ABSTRACT
During neural development, the actin filament network must be precisely regulated to form elaborate neurite structures. N-WASP tightly controls actin polymerization dynamics by activating an actin nucleator Arp2/3. However, the importance of N-WASP-Arp2/3 signaling in the assembly of neurite architecture in vivo has not been clarified. Here, we demonstrate that N-WASP-Arp2/3 signaling plays a crucial role in the maturation of cerebellar Purkinje cell (PC) dendrites in vivo in mice. N-WASP was expressed and activated in developing PCs. Inhibition of Arp2/3 and N-WASP from the beginning of dendrite formation severely disrupted the establishment of a single stem dendrite, which is a characteristic basic structure of PC dendrites. Inhibition of Arp2/3 after stem dendrite formation resulted in hypoplasia of the PC dendritic tree. Cdc42, an upstream activator of N-WASP, is required for N-WASP-Arp2/3 signaling-mediated PC dendrite maturation. In addition, overactivation of N-WASP is also detrimental to dendrite formation in PCs. These findings reveal that proper activation of N-WASP-Arp2/3 signaling is crucial for multiple steps of PC dendrite maturation in vivo.
Funder
Japan Society for the Promotion of Science
Takeda Science Foundation
Naito Foundation
Life Science Foundation of Japan
Kawano Masanori Memorial Public Interest Incorporated Foundation
NOVARTIS Foundation (Japan) for the Promotion of Science
Publisher
The Company of Biologists
Subject
Developmental Biology,Molecular Biology
Cited by
5 articles.
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