TGFβ ligands promote the initiation of retinal ganglion cell dendrites in vitro and in vivo

被引:33
作者
Hocking, Jennifer C. [1 ]
Hehr, Carrie L. [1 ]
Chang, Ruoh-Yeng [1 ]
Johnston, Jillian [1 ]
McFarlane, Sarah [1 ]
机构
[1] Univ Calgary, Hotchkiss Brain Inst, Calgary, AB T2N 4N1, Canada
基金
加拿大健康研究院; 加拿大自然科学与工程研究理事会; 加拿大创新基金会;
关键词
TGF beta; BMP; GDF; Xenopus; dendrite development;
D O I
10.1016/j.mcn.2007.09.011
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Each type of neuron develops a unique morphology critical to its function, but almost all start with the basic plan of one long axon and multiple short, branched dendrites. Though extrinsic signals are known to direct many steps in the development of neuronal structure, little is understood about the initiation of processes, particularly dendrites. We find that Xenopus retinal ganglion cells (RGCs) explanted early will extend axons and not dendrites in dissociated cultures. If RGCs develop longer in vivo prior to culturing, many now extend dendrite-like processes in vitro, suggesting that an extrinsic factor is required to stimulate dendrite initiation. Members of the transforming growth factor beta (TGF beta) superfamily, bone morphogenetic protein 2 (BMP2), and growth and differentiation factor 11 (GDF11), can signal cultured RGCs to form dendrites. Furthermore, TGF beta ligands have an endogenous role: blocking BMP/GDF signaling with a secreted antagonist or inhibitory receptors reduces the number of primary dendrites extended in vivo. (C) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:247 / 260
页数:14
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