Bi-directional control of motor neuron dendrite remodeling by the calcium permeability of AMPA receptors

被引:16
作者
Jeong, Goo-Bo
Werner, Markus
Gazula, Valeswara-Rao
Itoh, Takayuki
Roberts, Melinda
David, Samuel
Pfister, Bryan
Cohen, Akiva
Neve, Rachael L.
Hollmann, Michael
Kalb, Robert
机构
[1] Univ Penn, Sch Med, Dept Neurol, Childrens Hosp Philadelphia,Abramson Res Ctr, Philadelphia, PA 19104 USA
[2] Chungbuk Natl Univ, Coll Med, Dept Anat, Cheongju 361763, South Korea
[3] Ruhr Univ Bochum, Dept Biochem I Receptor Biochem, D-44780 Bochum, Germany
[4] Yale Univ, Sch Med, Dept Neurobiol, New Haven, CT 06511 USA
[5] Univ Penn, Sch Med, Dept Neurosurg, Philadelphia, PA 19104 USA
[6] Harvard Univ, Sch Med, Dept Psychiat, Belmont, MA 02478 USA
关键词
GluR1; spinal cord; activity-dependent plasticity; calcium; herpes simplex virus; transgene; calcineurin;
D O I
10.1016/j.mcn.2006.04.008
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Motor neurons express particularly high levels of the AMPA receptor subunit GluR1(Q)flip (GluR1(Q)i) during the period in early postnatal life when their dendritic tree grows and becomes more branched. To investigate how GluR1-containing AMPA receptors contribute to dendrite morphogenesis, we characterized a mutant form of GluR1 (containing a histidine in the Q/R editing site) with unique electrophysiological properties. Most notably, AMPA receptors assembled from GluR1(H)i display less calcium permeability than AMPA receptors assembled from GluR1(Q)i. Expression of GluR1(Q)i in vivo or in vitro led to an increase in dendrite branching with no net change in the overall tree size while GluR1(H)i led to a loss of branches and a net reduction in overall tree size. GluR1(H)i-dependent dendrite atrophy is mediated by protein phosphatase 2B. The results suggest that the electrophysiological properties of cell surface AMPA receptors, specifically their permeability to calcium, can be a central determinant of whether the dendrites undergo activity-dependent branching or atrophy. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:299 / 314
页数:16
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