TY - JOUR
T1 - Speed control for neuronal migration in the postnatal brain by Gmip-mediated local inactivation of RhoA
AU - Ota, Haruko
AU - Hikita, Takao
AU - Sawada, Masato
AU - Nishioka, Tomoki
AU - Matsumoto, Mami
AU - Komura, Masayuki
AU - Ohno, Akihisa
AU - Kamiya, Yukiyo
AU - Miyamoto, Takuya
AU - Asai, Naoya
AU - Enomoto, Atsushi
AU - Takahashi, Masahide
AU - Kaibuchi, Kozo
AU - Sobue, Kazuya
AU - Sawamoto, Kazunobu
PY - 2014/7/30
Y1 - 2014/7/30
N2 - Throughout life, new neurons generated in the ventricular-subventricular zone take the long journey to the olfactory bulb. The intracellular mechanisms that precisely control the neuronsâ (tm) migration speed, enabling their well-organized movement, remain unclear. Rho signalling is known to affect the morphology and movement of various cell types, including neurons. Here we identify Gem-interacting protein (Gmip), a RhoA-specific GTPase-activating protein, as a key factor in saltatory neuronal migration. RhoA is activated at the proximal leading process of migrating neurons, where Gmip is also localized and negatively regulates RhoA. Gmip controls the saltatory movement of neurons that regulate their migration speed and â ̃ stopâ (tm) positions in the olfactory bulb, thereby altering the neural circuitry. This study demonstrates that Gmip serves as a brake for the RhoA-mediated movement of neuronal somata, and highlights the significance of speed control in the well-organized neuronal migration and the maintenance of neuronal circuits in the postnatal brain.
AB - Throughout life, new neurons generated in the ventricular-subventricular zone take the long journey to the olfactory bulb. The intracellular mechanisms that precisely control the neuronsâ (tm) migration speed, enabling their well-organized movement, remain unclear. Rho signalling is known to affect the morphology and movement of various cell types, including neurons. Here we identify Gem-interacting protein (Gmip), a RhoA-specific GTPase-activating protein, as a key factor in saltatory neuronal migration. RhoA is activated at the proximal leading process of migrating neurons, where Gmip is also localized and negatively regulates RhoA. Gmip controls the saltatory movement of neurons that regulate their migration speed and â ̃ stopâ (tm) positions in the olfactory bulb, thereby altering the neural circuitry. This study demonstrates that Gmip serves as a brake for the RhoA-mediated movement of neuronal somata, and highlights the significance of speed control in the well-organized neuronal migration and the maintenance of neuronal circuits in the postnatal brain.
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U2 - 10.1038/ncomms5532
DO - 10.1038/ncomms5532
M3 - Article
C2 - 25074242
AN - SCOPUS:84905252070
SN - 2041-1723
VL - 5
JO - Nature communications
JF - Nature communications
M1 - 4532
ER -