Investigating Neotenic and Metamorphic Axolotl Brain Complexity: A Stereological and Immunohistochemical Perspective

IF 2.3 4区 医学 Q3 NEUROSCIENCES
Arife Ahsen Kaplan, Gürkan Öztürk, Sadık Bay, İlknur Keskin
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Abstract

The ability of certain tetrapods, such as amphibians, to regenerate complex structures, such as organs or limbs, is well-established, though this capacity varies significantly across species, with humans exhibiting limited regenerative potential. Ependymoglia cells in the ventricular region of the brain are known to exhibit proliferative properties during homeostasis and damage and to perform stem cell functions. This study investigated changes occurring in neurons and glia in the central nervous system following metamorphosis in axolotls. Morphological alterations in brain tissue, newly formed neurons, and cellular organizations in different brain regions were assessed using stereological and immunohistochemical methods, as well as light and electron microscopy. Interestingly, we observe no statistically significant difference in total neuron numbers in the telencephalon region between neotenic and metamorphic axolotls. However, the proliferation index and the numbers of cells expressing NeuN were significantly higher in metamorphic axolotls. Furthermore, structural changes in neuronal nuclei and myelin sheath organization were determined at the light and electron microscopic levels post-metamorphosis. Ultrastructural analyses revealed a change in chromatin organization from euchromatic to heterochromatic in neurons after metamorphosis, and morphological changes were also demonstrated in myelinated nerve fibers in the telencephalon. Additionally, mucopolysaccharide-containing secretory sacs were also identified on the apical surfaces of a subgroup of ependymoglia cells located in the lateral ventricle wall. Overall, this study sheds useful light on the intricate changes occurring in the central nervous system during metamorphosis in axolotls and provides valuable insights into the mechanisms underlying these processes.

Abstract Image

从体视学和免疫组织化学的角度研究新生和变质蝾螈大脑的复杂性。
某些四足动物,如两栖动物,再生复杂结构(如器官或四肢)的能力是公认的,尽管这种能力在不同物种之间差异很大,人类表现出有限的再生潜力。已知脑室区的室管膜胶质细胞在稳态和损伤期间表现出增殖特性,并具有干细胞功能。本研究探讨了蝾螈变态后中枢神经系统神经元和胶质细胞的变化。使用体视学和免疫组织化学方法以及光学和电子显微镜评估脑组织,新形成的神经元和不同脑区域的细胞组织的形态学改变。有趣的是,我们观察到幼幼期和变质期蝾螈在端脑区总神经元数量上没有统计学上的显著差异。而异变蝾螈的增殖指数和表达NeuN的细胞数量明显高于异变蝾螈。此外,在光镜和电镜下观察了变形后神经元核和髓鞘组织的结构变化。超微结构分析显示,变形后神经元染色质由正染色质变为异染色质,远脑髓鞘神经纤维也发生了形态变化。此外,在位于侧脑室壁的室管膜胶质细胞亚群的顶端表面也发现了含有粘多糖的分泌囊。总的来说,这项研究揭示了美西螈变态过程中中枢神经系统发生的复杂变化,并为这些过程的潜在机制提供了有价值的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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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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