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猕猴视网膜中表达小白蛋白免疫反应性的无长突细胞

Parvalbumin-immunoreactive amacrine cells of macaque retina.

作者信息

Klump Kathryn E, Zhang Ai-Jun, Wu Samuel M, Marshak David W

机构信息

Department of Neurobiology and Anatomy, University of Texas Medical School at Houston, Houston, Texas 77225, USA.

出版信息

Vis Neurosci. 2009 May-Jun;26(3):287-96. doi: 10.1017/S0952523809090075. Epub 2009 May 13.

Abstract

A number of authors have observed amacrine cells containing high levels of immunoreactive parvalbumin in primate retinas. The experiments described here were designed to identify these cells morphologically, to determine their neurotransmitter, to record their light responses, and to describe the other cells that they contact. Macaque retinas were fixed in paraformaldehyde and labeled with antibodies to parvalbumin and one or two other markers, and this double- and triple-labeled material was analyzed by confocal microscopy. In their morphology and dendritic stratification patterns, the parvalbumin-positive cells closely resembled the knotty type 2 amacrine cells described using the Golgi method in macaques. They contained immunoreactive glycine transporter, but not immunoreactive gamma-aminobutyric acid, and therefore, they use glycine as their neurotransmitter. Their spatial density was relatively high, roughly half that of AII amacrine cells. They contacted lobular dendrites of AII cells, and they are expected to be presynaptic to AII cells based on earlier ultrastructural studies. They also made extensive contacts with axon terminals of OFF midget bipolar cells whose polarity cannot be predicted with certainty. A macaque amacrine cell of the same morphological type depolarized at the onset of increments in light intensity, and it was well coupled to other amacrine cells. Previously, we described amacrine cells like these that contacted OFF parasol ganglion cells and OFF starburst amacrine cells. Taken together, these findings suggest that one function of these amacrine cells is to inhibit the transmission of signals from rods to OFF bipolar cells via AII amacrine cells. Another function may be inhibition of the OFF pathway following increments in light intensity.

摘要

许多作者在灵长类动物视网膜中观察到含有高水平免疫反应性小白蛋白的无长突细胞。本文所述实验旨在从形态学上识别这些细胞,确定其神经递质,记录其光反应,并描述它们所接触的其他细胞。猕猴视网膜用多聚甲醛固定,并用针对小白蛋白和一种或两种其他标记物的抗体进行标记,然后通过共聚焦显微镜分析这种双重和三重标记的材料。在形态和树突分层模式上,小白蛋白阳性细胞与用高尔基方法在猕猴中描述的结节状2型无长突细胞非常相似。它们含有免疫反应性甘氨酸转运体,但不含免疫反应性γ-氨基丁酸,因此,它们使用甘氨酸作为神经递质。它们的空间密度相对较高,大约是AII无长突细胞的一半。它们与AII细胞的小叶状树突接触,根据早期的超微结构研究,预计它们是AII细胞的突触前细胞。它们还与OFF侏儒双极细胞的轴突终末广泛接触,而OFF侏儒双极细胞的极性无法确定预测。同一形态类型的猕猴无长突细胞在光强度增加开始时去极化,并且与其他无长突细胞紧密耦合。此前,我们描述过这样的无长突细胞,它们与OFF伞状神经节细胞和OFF爆发性无长突细胞接触。综上所述,这些发现表明这些无长突细胞的一个功能是抑制信号从视杆细胞通过AII无长突细胞向OFF双极细胞的传递。另一个功能可能是在光强度增加后抑制OFF通路。

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Parvalbumin-immunoreactive amacrine cells of macaque retina.猕猴视网膜中表达小白蛋白免疫反应性的无长突细胞
Vis Neurosci. 2009 May-Jun;26(3):287-96. doi: 10.1017/S0952523809090075. Epub 2009 May 13.

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