Spatial Distribution and Morphology of CaMKII-Expressing Amacrine Cells in Marmoset, Macaque, and Human Retina

IF 2.3 4区 医学 Q3 NEUROSCIENCES
Alyssa K. Baldicano, Paul R. Martin, Ulrike Grünert
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Abstract

Over 30 types of amacrine cells have been described in the primate retina, yet few are well characterized. Here, we investigated amacrine cells expressing the alpha subunit of calcium/calmodulin-dependent protein kinase II (CaMKII) in the retinas of human, macaque (Macaca fascicularis, Macaca nemestrina), and marmoset (Callithrix jacchus) monkeys using immunohistochemistry and intracellular injections, with a focus on displaced amacrine cells (dACs) in the ganglion cell layer. The spatial density of CaMKII-positive dACs decreases with the distance from the fovea, but in the peripheral temporal retina, the density of CaMKII-positive dACs nevertheless exceeds the density of retinal ganglion cells. In all species, CaMKII-positive dACs include cells expressing choline acetyltransferase (ChAT) cells, but in the human retina, only 60% of the ON ChAT population is CaMKII-positive. Conversely, in the marmoset and the macaque, about 80% of ON ChAT cells co-express CaMKII, but only 55% of ON ChAT cells in humans do so. Intracellular injections of CaMKII-positive dACs with the lipophilic dye DiI revealed ON starburst and semilunar Type 3 cells in all three species, but in the human retina, at least three additional types were detected. In the inner nuclear layer, CaMKII is expressed by multiple populations of amacrine cells, which are distinguished based on their soma size and staining intensity, but OFF ChAT cells do not co-express CaMKII. We conclude that ON- and OFF-ChAT cells show distinct patterns of CaMKII expression and that the diversity of CaMKII-expressing dACs in humans is greater than that in marmoset or macaque retina.

Abstract Image

表达camkii的无毛细胞在狨猴、猕猴和人视网膜中的空间分布和形态
在灵长类动物的视网膜中,已有超过30种类型的无毛细胞被描述,但很少有很好的特征。在这里,我们使用免疫组织化学和细胞内注射的方法研究了人类、猕猴(Macaca fascicularis, Macaca nemestrina)和狨猴(Callithrix jacchus)视网膜中表达钙/钙调素依赖性蛋白激酶II (CaMKII) α亚基的无毛细胞,重点研究了神经节细胞层中移位的无毛细胞(dACs)。camkii阳性dACs的空间密度随离中央凹的距离而减小,但在颞外周视网膜,camkii阳性dACs的密度仍然超过视网膜神经节细胞的密度。在所有物种中,camkii阳性的dac包括表达胆碱乙酰转移酶(ChAT)的细胞,但在人类视网膜中,只有60%的ON ChAT群体是camkii阳性的。相反,在狨猴和猕猴中,大约80%的ON ChAT细胞共同表达CaMKII,但在人类中只有55%的ON ChAT细胞这样做。细胞内注射camkii阳性的带有亲脂性染料DiI的dac,在所有三种细胞中都发现了ON星爆型和半月型3细胞,但在人类视网膜中,至少检测到另外三种类型。在内核层,CaMKII在多个无毛细胞群中表达,根据它们的体细胞大小和染色强度来区分,但OFF ChAT细胞不共表达CaMKII。我们得出结论,ON-和OFF-ChAT细胞表现出不同的CaMKII表达模式,并且人类中表达CaMKII的dac的多样性大于狨猴或猕猴视网膜。
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来源期刊
CiteScore
5.80
自引率
8.00%
发文量
158
审稿时长
3-6 weeks
期刊介绍: Established in 1891, JCN is the oldest continually published basic neuroscience journal. Historically, as the name suggests, the journal focused on a comparison among species to uncover the intricacies of how the brain functions. In modern times, this research is called systems neuroscience where animal models are used to mimic core cognitive processes with the ultimate goal of understanding neural circuits and connections that give rise to behavioral patterns and different neural states. Research published in JCN covers all species from invertebrates to humans, and the reports inform the readers about the function and organization of nervous systems in species with an emphasis on the way that species adaptations inform about the function or organization of the nervous systems, rather than on their evolution per se. JCN publishes primary research articles and critical commentaries and review-type articles offering expert insight in to cutting edge research in the field of systems neuroscience; a complete list of contribution types is given in the Author Guidelines. For primary research contributions, only full-length investigative reports are desired; the journal does not accept short communications.
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