小型回声定位蝙蝠的海马体结构、钙结合蛋白模式和神经元数量。

IF 2.3 4区 医学 Q1 ANATOMY & MORPHOLOGY
Frontiers in Neuroanatomy Pub Date : 2025-08-13 eCollection Date: 2025-01-01 DOI:10.3389/fnana.2025.1641787
Jovana Maliković, Katja Schönbächler, Ana Luiza F Destro, David P Wolfer, Irmgard Amrein
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引用次数: 0

摘要

尽管蝙蝠是种类第二多的哺乳动物,但对它们海马体的神经解剖学研究却很少,尤其是对小型回声定位蝙蝠的研究。在此,我们对小型回声定位蝙蝠(Phyllostomidae和Vespertilionidae)的海马进行了定性和定量的神经解剖学分析。钙结合蛋白揭示了钙结合蛋白和钙降钙蛋白的物种和家族特异性模式。这两种蛋白的中间神经元染色在层状气孔类动物中非常罕见,而calretinin标记了两个科的CA3锥体神经元亚群。小白蛋白的表达在蝙蝠中是一致的,与其他物种相似。在层状体蝙蝠CA3锥体细胞层的表面边界处,观察到一个独特的calretinin阳性calretinin阴性区。这个区域定义了锥体细胞和带锌的苔藓纤维之间的间隙。我们假设这种间隙可能是由于calretinin阳性传入取代了锌阳性的苔藓纤维束,或者是由于神经化学上不同的苔藓束的完全分离。此外,我们观察到颗粒细胞层的上下叶片长度在所有物种中都有明显的背腹移动。在海马神经元数量方面,蝙蝠的特点是颗粒细胞和棘下神经元数量较少,但CA3发育良好。在对应分析中,偏好饮食将层状气孔虫分为门状优势杂食性和果食性类群,以及门状下优势类群,包括吸血蝙蝠和食性类群。虽然这两个科有很大的重叠,但叶状体海马的细胞组成可以被描述为输出为主,而在海马体输入侧的超列类神经元群则更占优势。这里所示的回声定位蝙蝠的神经解剖和生态变异以及独特的特征可以为研究结构-功能关系提供丰富的资源。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Hippocampal structure, patterns of the calcium-binding proteins and neuron numbers in small echolocating bats.

Even though bats are the second most speciose group of mammals, neuroanatomical studies of their hippocampus are rare, particularly of small echolocating bats. Here, we provide a qualitative and quantitative neuroanatomical analysis of the hippocampus of small echolocating bats (Phyllostomidae and Vespertilionidae). Calcium-binding proteins revealed species- and family-specific patterns for calbindin and calretinin. Interneuron staining for both proteins was very rare in phyllostomids, while calretinin marked subpopulations of CA3 pyramidal neurons in both families. Parvalbumin expression was consistent across bats and similar to other species. A unique calretinin-positive calbindin-negative zone was observed at the superficial boundary of the CA3 pyramidal cell layer in phyllostomid bats. This zone defined a gap between pyramidal cells and the zinc-positive mossy fibers. We hypothesize that this gap might either stem from calretinin-positive afferents displacing the zinc-positive mossy fiber boutons, or from a complete segregation of neurochemically distinct mossy boutons. Furthermore, we observed a distinct dorsoventral shift in the length of the upper and lower blade of the granule cell layer in all species. In terms of hippocampal neuron numbers, bats were characterized by a rather small granule cell and subicular neuron population, but a well-developed CA3. In a correspondence analysis, preferred diet segregated phyllostomids into a hilus-dominant omnivorous and frugivorous species group, and a subiculum-dominant group containing vampire bats and nectivorous species. Although the two families overlapped considerably, the cellular composition of the phyllostomid hippocampus can be described as output dominant, while in vespertilionids neuron populations on the hippocampal input side are more dominant. Neuroanatomical and ecological variability and unique traits within echolocating bats as shown here can provide a rich source for investigating structure-function relationships.

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来源期刊
Frontiers in Neuroanatomy
Frontiers in Neuroanatomy ANATOMY & MORPHOLOGY-NEUROSCIENCES
CiteScore
4.70
自引率
3.40%
发文量
122
审稿时长
>12 weeks
期刊介绍: Frontiers in Neuroanatomy publishes rigorously peer-reviewed research revealing important aspects of the anatomical organization of all nervous systems across all species. Specialty Chief Editor Javier DeFelipe at the Cajal Institute (CSIC) is supported by an outstanding Editorial Board of international experts. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide.
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