Non-cell-autonomous factor induces the transition from excitatory to inhibitory GABA signaling in retina independent of activity

被引:13
作者
Barkis, William B. [1 ,2 ,3 ]
Ford, Kevin J. [1 ,2 ]
Feller, Marla B. [1 ,2 ]
机构
[1] Univ Calif Berkeley, Dept Mol & Cell Biol, Berkeley, CA 94720 USA
[2] Univ Calif Berkeley, Helen Wills Neurosci Inst, Berkeley, CA 94720 USA
[3] Univ Calif San Diego, Grad Program Neurosci, San Diego, CA 92093 USA
基金
美国国家卫生研究院;
关键词
muscimol; nicotinic acetylcholine receptor; retinal waves; calcium imaging; BDNF; CL-COTRANSPORTER KCC2; GANGLION-CELLS; ACCUMULATE CHLORIDE; MICE LACKING; NEURONS; EXPRESSION; SWITCH; MODULATION; NKCC1; NA+;
D O I
10.1073/pnas.1008775108
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
During development, the effect of activating GABA(A) receptors switches from depolarizing to hyperpolarizing. Several environmental factors have been implicated in the timing of this GABA switch, including neural activity, although these observations remain controversial. By using acutely isolated retinas from KO mice and pharmacological manipulations in retinal explants, we demonstrate that the timing of the GABA switch in retinal ganglion cells (RGCs) is unaffected by blockade of specific neurotransmitter receptors or global activity. In contrast to RGCs in the intact retina, purified RGCs remain depolarized by GABA, indicating that the GABA switch is not cell-autonomous. Indeed, purified RGCs cocultured with dissociated cells from the superior colliculus or cultured in media conditioned by superior collicular cells undergo a normal switch. Thus, a diffusible signal that acts independent of local circuit activity regulates the maturation of GABAergic inhibition in mouse RGCs.
引用
收藏
页码:22302 / 22307
页数:6
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