Famiglietti Edward V, Sundquist Sarah J
Department of Surgery (Ophthalmology), Brown University, Providence, Rhode Island 02882, USA.
Vis Neurosci. 2010 Mar;27(1-2):19-42. doi: 10.1017/S0952523810000052. Epub 2010 Apr 15.
Starburst amacrine cells (SACs), the only acetylcholine (ACh)-releasing amacrine cells (ACs) in adult rabbit retina, contain GABA and are key elements in the retina's directionally selective (DS) mechanism. Unlike many other GABAergic ACs, they use glutamic acid decarboxlyase (GAD)(67), not GAD(65), to synthesize GABA. Using immunocytochemistry, we demonstrate the apoptosis at birth (P0) of transitory putative ACs that exhibit immunoreactivity (IR) for the ACh-synthetic enzyme choline acetyltransferase (ChAT), GAD(67), and the GABA transporter, GAT1. Only a few intact, displaced ChAT-immunoreactive SAC bodies are detected at P0. At P2, ChAT-IR is detected in the two narrowly stratified substrata of starburst dendrites in the inner plexiform layer (IPL). Quantitative analysis reveals that in the first postnatal week, only a small fraction of SACs cells express ChAT- and GABA-IR. Not until the end of the second week are they expressed in all SACs. At P0, a three-tiered stratification of GABA-IR is present in the IPL, entirely different from the adult pattern of seven substrata, emerging at P3-P4, and optimally visualized at P13. At P0, GAD(65) is detectable in normally placed AC bodies. At P1, GAD(65)-IR appears in dendrites of nonstarburst GABAergic ACs, and by P5 is robust in the adult pattern of four substrata in the IPL. GAD(65)-IR never co-localizes with ChAT-IR. In a temporal comparison of our data with physiological, pharmacological, and ultrastructural studies, we suggest that transitory ChAT-immunoreactive cells share with SACs production of stage II (nicotinic) waves of previsual synchronous activity in ganglion cells (GCs). Further, we conclude that (1) GAD(65)-immunoreactive, non-SAC GABAergic ACs are the most likely candidates responsible for the suppression of stage III (muscarinic/AMPA-kainate) waves and (2) DS responses first appear in DS GCs, when about 50% of SACs express ChAT- and GABA-IR, and in 100% of DS GCs, when expression occurs in all SACs.
星爆无长突细胞(SACs)是成年兔视网膜中唯一释放乙酰胆碱(ACh)的无长突细胞(ACs),含有γ-氨基丁酸(GABA),是视网膜方向选择性(DS)机制的关键元件。与许多其他GABA能ACs不同,它们利用谷氨酸脱羧酶(GAD)(67)而非GAD(65)来合成GABA。我们运用免疫细胞化学方法,证实了出生时(P0)短暂存在的假定ACs发生凋亡,这些细胞对ACh合成酶胆碱乙酰转移酶(ChAT)、GAD(67)以及GABA转运体GAT1呈现免疫反应性(IR)。在P0时,仅检测到少数完整的、移位的ChAT免疫反应性SAC胞体。在P2时,在内网状层(IPL)中星爆树突的两个狭窄分层亚层中检测到ChAT-IR。定量分析显示,在出生后的第一周,只有一小部分SAC细胞表达ChAT-和GABA-IR。直到第二周结束,它们才在所有SAC中表达。在P0时,IPL中存在GABA-IR的三层分层,与成年时的七层亚层模式完全不同,后者在P3 - P4出现,并在P13时最佳显示。在P0时,正常位置的AC胞体中可检测到GAD(65)。在P1时,GAD(65)-IR出现在非星爆GABA能ACs的树突中,到P5时,在IPL中成年模式的四个亚层中表现强烈。GAD(65)-IR从未与ChAT-IR共定位。在将我们的数据与生理学、药理学和超微结构研究进行时间比较时,我们认为短暂的ChAT免疫反应性细胞与SACs共同参与神经节细胞(GCs)中视觉前同步活动II期(烟碱样)波的产生。此外,我们得出结论:(1)GAD(65)免疫反应性、非SAC GABA能ACs最有可能是负责抑制III期(毒蕈碱样/AMPA-海人藻酸)波的细胞;(2)DS反应首先出现在DS GCs中,此时约50%的SACs表达ChAT-和GABA-IR,而在所有SACs都表达时,DS反应出现在100%的DS GCs中。