Long-range retrograde spread of LTP and LTD from optic tectum to retina

被引:35
作者
Du, Jiu-lin [1 ,2 ,3 ]
Wei, Hong-ping [2 ,3 ]
Wang, Zuo-ren [1 ,2 ,3 ]
Wong, Scott T. [1 ]
Poo, Mu-ming [1 ]
机构
[1] Univ Calif Berkeley, Helen Wills Neurosci Inst, Dept Mol & Cell Biol, Div Neurobiol, Berkeley, CA 94720 USA
[2] Chinese Acad Sci, Shanghai Inst Biol Sci, Inst Neurosci, Shanghai 200031, Peoples R China
[3] Chinese Acad Sci, Shanghai Inst Biol Sci, Key State Lab Neurosci, Shanghai 200031, Peoples R China
基金
美国国家卫生研究院;
关键词
neural development; retrograde signaling; synaptic plasticity; retinal ganglion cell; PRESYNAPTIC NEURONAL EXCITABILITY; DEVELOPING RETINOTECTAL SYSTEM; REMODELING IN-VIVO; TERM POTENTIATION; NEUROTROPHIC FACTOR; SYNAPTIC PLASTICITY; LASTING POTENTIATION; MAMMALIAN BRAIN; NEURAL-NETWORKS; VISUAL-SYSTEM;
D O I
10.1073/pnas.0910659106
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Neural activity can induce persistent strengthening or weakening of synapses, known as long-term potentiation (LTP) or long-term depression (LTD), respectively. As potential cellular mechanisms underlying learning and memory, LTP and LTD are generally regarded as synapse-specific "imprints'' of activity, although there is evidence in vitro that LTP/LTD may spread to adjacent synapses. Here, we report that LTP and LTD induced in vivo at retinotectal synapses of Xenopus tadpoles undergo rapid long-range retrograde spread from the optic tectum to the retina, resulting in potentiation and depression of bipolar cell synapses on the dendrites of retinal ganglion cells, respectively. The retrograde spread of LTP and LTD required retrograde signaling initiated by brain-derived neurotrophic factor and nitric oxide in the tectum, respectively. Such bidirectional adjustment of the strength of input synapses in accordance to that of output synapses may serve to coordinate developmental refinement and learning functions of neural circuits.
引用
收藏
页码:18890 / 18896
页数:7
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