红耳滑龟的皮肤神经支配:鳞片感受器和感觉小体的免疫荧光识别和分析及其生态学意义。

IF 1.9 3区 生物学 Q1 ZOOLOGY
Ahmed M Rashwan, Samir A A El-Gendy, Samar M Ez Elarab, Manal Seif, Ahmed A El-Mansi, Mamdouh B Eldesoqui, Mohamed A M Alsafy
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引用次数: 0

摘要

红耳滑龟生活在淡水到半陆地的各种环境中。了解这个物种的感觉适应是至关重要的,特别是关于它的肢体皮肤,它在环境相互作用和生存中起着关键作用。本研究首次详细鉴定了红耳滑鼠肢体皮肤的鳞片感受器和感觉小体,对它们的神经支配和分布有了深入的了解。结合扫描电镜、光镜、免疫荧光等方法,研究了海龟皮肤的感觉结构和适应机制。这些抗体包括E-cadherin、4种神经标记物(Nestin、PGP9.5、神经元特异性烯醇酶[NSE]和Synaptophysin)和5种附加标记物(PDGFRα、CD34、Vimentin、α-SMA和Tom20),用于分析感觉结构和分布模式。扫描电镜显示了类似洋蓟的鳞状感受器,其同心层围绕着一个具有微皱膜、沟槽和孔的中央圆顶。光镜显示,这些感觉器为表皮表面上方的圆顶状结构。E-cadherin的免疫荧光显示鳞状感受器细胞、中枢细胞和真皮乳头,而神经标记证实了鳞状感受器内的感觉神经,强调了它们的感觉作用。肢体皮肤中存在三种感觉小体:真皮层的Meissner’s和Ruffini小体,皮下的Pacinian小体。这四种神经标记在感觉神经纤维末梢的所有小体中都有强烈的表达,突出了它们在检测压力、振动和触觉刺激中的作用。CD34和PDGFRα在Pacinian小体外囊和同心圆片内的神经周围成纤维细胞样细胞和远端细胞以及Meissner小体和Ruffini小体外囊内表达,并在这三种类型的远端细胞周围表达。在所有小体的结缔组织和板层细胞中均发现了维门蛋白,提示其在结构支撑中起作用。α-SMA在太平洋小体中表达强烈,在迈斯纳小体和鲁菲尼小体中表达较少,表明其在维持太平洋小体结构完整性中起主要作用。Tom20在所有小体的神经纤维和支持细胞中显示出较高的线粒体活性,在迈斯纳小体中表达最高,反映了这些感觉结构的显著代谢需求。这项研究为红耳滑龟皮肤的感官结构提供了前所未有的见解。对鳞状感受器和感觉小体的新鉴定和分析,结合10种抗体,增强了我们对皮肤神经支配及其在环境适应中的作用的理解,为感觉生物学和爬行学贡献了宝贵的知识。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cutaneous Innervation in the Red-Eared Slider Turtle: Novel Identification and Analysis of Scale Sensilla and Sensory Corpuscles With Immunofluorescence Insights and Ecological Implications.

The red-eared slider turtle inhabits environments ranging from freshwater to semiterrestrial settings. Understanding the sensory adaptations of this species is crucial, particularly concerning its limb skin, which plays a key role in environmental interaction and survival. This study presents the first detailed identification of scale sensilla and sensory corpuscles in the red-eared slider's limb skin, offering insights into their innervation and distribution. We combined scanning electron microscopy (SEM), light microscopy, and immunofluorescence with ten antibodies to elucidate the sensory architecture and adaptation mechanisms of the turtle's skin. The antibodies include E-cadherin, four neural markers (Nestin, PGP9.5, neuron-specific enolase [NSE], and Synaptophysin), and five additional markers (PDGFRα, CD34, Vimentin, α-SMA, and Tom20) to analyze sensory structures and distribution patterns. SEM revealed scale sensilla resembling artichokes, with concentric layers surrounding a central dome featuring microplicae, grooves, and pores. Light microscopy showed these sensilla as dome-shaped structures elevated above the epidermal surface. Immunofluorescence with E-cadherin highlighted scale sensilla cells, central cells, and dermal papillae, while neural markers confirmed sensory nerves within the scale sensilla, underscoring their sensory role. Three types of sensory corpuscles were identified in the limb skin: Meissner's and Ruffini corpuscles in the dermis, and Pacinian corpuscles in the hypodermis. The four neural markers showed strong expression in sensory nerve fiber endings across all corpuscles, highlighting their roles in detecting pressure, vibration, and tactile stimuli. CD34 and PDGFRα were expressed in perineurial fibroblast-like cells and telocytes within the external capsules and concentric lamellae of Pacinian corpuscles, as well as in the external capsules of Meissner's and Ruffini corpuscles, with telocytes surrounding all three types. Vimentin was found in connective tissue and lamellar cells in all corpuscles, suggesting its role in structural support. α-SMA was strongly expressed in Pacinian corpuscles and minimally in Meissner's and Ruffini corpuscles, indicating its primary role in maintaining structural integrity in Pacinian corpuscles. Tom20 highlighted high mitochondrial activity in the nerve fibers and supporting cells of all corpuscles, with the highest expression in Meissner's corpuscles, reflecting the significant metabolic demands of these sensory structures. This study offers unprecedented insights into the sensory architecture of the red-eared slider turtle's skin. The novel identification and analysis of scale sensilla and sensory corpuscles, combined with 10 antibodies, enhances our understanding of the skin's innervation and its role in environmental adaptation, contributing valuable knowledge to sensory biology and herpetology.

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来源期刊
Journal of experimental zoology. Part A, Ecological and integrative physiology
Journal of experimental zoology. Part A, Ecological and integrative physiology Biochemistry, Genetics and Molecular Biology-Molecular Biology
CiteScore
4.90
自引率
3.60%
发文量
0
期刊介绍: The Journal of Experimental Zoology – A publishes articles at the interface between Development, Physiology, Ecology and Evolution. Contributions that help to reveal how molecular, functional and ecological variation relate to one another are particularly welcome. The Journal publishes original research in the form of rapid communications or regular research articles, as well as perspectives and reviews on topics pertaining to the scope of the Journal. Acceptable articles are limited to studies on animals.
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