Haynes Elizabeth M, Ulland Tyler K, Eliceiri Kevin W
Morgridge Institute for Research, Madison, WI, United States.
Center for Quantitative Cell Imaging, University of Wisconsin-Madison, Madison, WI, United States.
Front Mol Neurosci. 2022 Apr 14;15:867010. doi: 10.3389/fnmol.2022.867010. eCollection 2022.
Rodents have been the dominant animal models in neurobiology and neurological disease research over the past 60 years. The prevalent use of rats and mice in neuroscience research has been driven by several key attributes including their organ physiology being more similar to humans, the availability of a broad variety of behavioral tests and genetic tools, and widely accessible reagents. However, despite the many advances in understanding neurobiology that have been achieved using rodent models, there remain key limitations in the questions that can be addressed in these and other mammalian models. In particular, imaging in mammals at the cell-resolution level remains technically difficult and demands large investments in time and cost. The simpler nervous systems of many non-mammalian models allow for precise mapping of circuits and even the whole brain with impressive subcellular resolution. The types of non-mammalian neuroscience models available spans vertebrates and non-vertebrates, so that an appropriate model for most cell biological questions in neurodegenerative disease likely exists. A push to diversify the models used in neuroscience research could help address current gaps in knowledge, complement existing rodent-based bodies of work, and bring new insight into our understanding of human disease. Moreover, there are inherent aspects of many non-mammalian models such as lifespan and tissue transparency that can make them specifically advantageous for neuroscience studies. Crispr/Cas9 gene editing and decreased cost of genome sequencing combined with advances in optical microscopy enhances the utility of new animal models to address specific questions. This review seeks to synthesize current knowledge of established and emerging non-mammalian model organisms with advances in cellular-resolution imaging techniques to suggest new approaches to understand neurodegeneration and neurobiological processes. We will summarize current tools and imaging approaches at the single cell scale that could help lead to increased consideration of non-mammalian models in neuroscience research.
在过去60年里,啮齿动物一直是神经生物学和神经疾病研究中占主导地位的动物模型。大鼠和小鼠在神经科学研究中的广泛应用得益于几个关键特性,包括它们的器官生理学与人类更为相似、有各种各样的行为测试和基因工具可供使用,以及试剂易于获取。然而,尽管使用啮齿动物模型在理解神经生物学方面取得了许多进展,但在这些模型以及其他哺乳动物模型中能够解决的问题仍然存在关键局限性。特别是,在哺乳动物中以细胞分辨率水平进行成像在技术上仍然困难,并且需要大量的时间和成本投入。许多非哺乳动物模型更简单的神经系统允许以令人印象深刻的亚细胞分辨率精确绘制神经回路甚至整个大脑的图谱。现有的非哺乳动物神经科学模型类型涵盖脊椎动物和非脊椎动物,因此可能存在一个适合神经退行性疾病中大多数细胞生物学问题的模型。推动神经科学研究中使用的模型多样化有助于填补当前的知识空白,补充现有的以啮齿动物为基础的研究工作,并为我们对人类疾病的理解带来新的见解。此外,许多非哺乳动物模型的固有特性,如寿命和组织透明度,可能使它们在神经科学研究中具有特殊优势。Crispr/Cas9基因编辑以及基因组测序成本的降低,再加上光学显微镜技术的进步,提高了新动物模型解决特定问题的效用。本综述旨在综合已建立和新兴的非哺乳动物模型生物的现有知识以及细胞分辨率成像技术的进展,以提出理解神经退行性变和神经生物学过程的新方法。我们将总结单细胞尺度上当前的工具和成像方法,这些方法可能有助于在神经科学研究中更多地考虑非哺乳动物模型。