棕蜥视网膜发育和重塑的组织学分析。

IF 1.8 3区 医学 Q2 ANATOMY & MORPHOLOGY
Ashley M Rasys, Shana H Pau, Katherine E Irwin, Sherry Luo, Hannah Q Kim, M Austin Wahle, Douglas B Menke, James D Lauderdale
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引用次数: 0

摘要

中央窝是视网膜上的一个凹坑,对人类的高灵敏度视力至关重要,在其他脊椎动物的眼睛中也有发现,包括某些灵长类动物、鸟类、蜥蜴和鱼类。尽管它对视觉很重要,但我们对中央凹发育机制的理解仍然有限。目前广泛应用的眼部研究模型缺乏凹形视网膜,对凹形视网膜发育的研究大多局限于灵长类动物的组织学和分子研究。作为阐明非灵长类脊椎动物中央窝发育的第一步,我们提出了一份详细的视网膜和中央窝发育的组织学图谱,该图谱是一种用于中央窝研究的新型爬行动物模型。我们测试了视网膜重塑,导致中央凹形成和光感受器细胞堆积,与眼睛形状的不对称变化有关的假设。我们的研究结果表明,在大多数脊椎动物中观察到的视网膜发育遵循典型的时空模式:视网膜神经发生始于中央视网膜,通过颞视网膜进展,并在鼻视网膜结束。然而,注定成为中央或颞中央凹的区域比视网膜的其他部分更早分化。我们观察到视网膜厚度在眼伸缩期的动态变化——伸缩期变薄,伸缩期变厚。此外,颞中央凹区神经节细胞层的短暂局部增厚正好发生在凹形成之前。我们的数据表明,变色蜥蜴视网膜的发育与人类相似,包括视网膜神经发生的发生和进展,随后是眼形状的变化和视网膜重塑导致坑形成。我们认为变色虫是研究中央窝发育的一个很好的模型系统。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Histological analysis of retinal development and remodeling in the brown anole lizard (Anolis sagrei).

The fovea, a pit in the retina, is crucial for high-acuity vision in humans and is found in the eyes of other vertebrates, including certain primates, birds, lizards, and fish. Despite its importance for vision, our understanding of the mechanisms involved in fovea development remains limited. Widely used ocular research models lack a foveated retina, and studies on fovea development are mostly limited to histological and molecular studies in primates. As a first step toward elucidating fovea development in nonprimate vertebrates, we present a detailed histological atlas of retina and fovea development in the bifoveated Anolis sagrei lizard, a novel reptile model for fovea research. We test the hypothesis that retinal remodeling, leading to fovea formation and photoreceptor cell packing, is related to asymmetric changes in eye shape. Our findings show that anole retina development follows the typical spatiotemporal patterning observed in most vertebrates: retinal neurogenesis starts in the central retina, progresses through the temporal retina, and finishes in the nasal retina. However, the areas destined to become the central or temporal fovea differentiate earlier than the rest of the retina. We observe dynamic changes in retinal thickness during ocular elongation and retraction-thinning during elongation and thickening during retraction. Additionally, a transient localized thickening of the ganglion cell layer occurs in the temporal fovea region just before pit formation. Our data indicate that anole retina development is similar to that of humans, including the onset and progression of retinal neurogenesis, followed by changes in ocular shape and retinal remodeling leading to pit formation. We propose that anoles are an excellent model system for fovea development research.

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来源期刊
Journal of Anatomy
Journal of Anatomy 医学-解剖学与形态学
CiteScore
4.80
自引率
8.30%
发文量
183
审稿时长
4-8 weeks
期刊介绍: Journal of Anatomy is an international peer-reviewed journal sponsored by the Anatomical Society. The journal publishes original papers, invited review articles and book reviews. Its main focus is to understand anatomy through an analysis of structure, function, development and evolution. Priority will be given to studies of that clearly articulate their relevance to the anatomical community. Focal areas include: experimental studies, contributions based on molecular and cell biology and on the application of modern imaging techniques and papers with novel methods or synthetic perspective on an anatomical system. Studies that are essentially descriptive anatomy are appropriate only if they communicate clearly a broader functional or evolutionary significance. You must clearly state the broader implications of your work in the abstract. We particularly welcome submissions in the following areas: Cell biology and tissue architecture Comparative functional morphology Developmental biology Evolutionary developmental biology Evolutionary morphology Functional human anatomy Integrative vertebrate paleontology Methodological innovations in anatomical research Musculoskeletal system Neuroanatomy and neurodegeneration Significant advances in anatomical education.
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