Pagella Pierfrancesco, Miran Shayee, Mitsiadis Tim
Institute of Oral Biology, Unit of Orofacial Development and Regeneration, University of Zurich.
Institute of Oral Biology, Unit of Orofacial Development and Regeneration, University of Zurich;
J Vis Exp. 2015 Aug 14(102):e53114. doi: 10.3791/53114.
Innervation plays a key role in the development, homeostasis and regeneration of organs and tissues. However, the mechanisms underlying these phenomena are not well understood yet. In particular, the role of innervation in tooth development and regeneration is neglected. Several in vivo studies have provided important information about the patterns of innervation of dental tissues during development and repair processes of various animal models. However, most of these approaches are not optimal to highlight the molecular basis of the interactions between nerve fibres and target organs and tissues. Co-cultures constitute a valuable method to investigate and manipulate the interactions between nerve fibres and teeth in a controlled and isolated environment. In the last decades, conventional co-cultures using the same culture medium have been performed for very short periods (e.g., two days) to investigate the attractive or repulsive effects of developing oral and dental tissues on sensory nerve fibres. However, extension of the culture period is required to investigate the effects of innervation on tooth morphogenesis and cytodifferentiation. Microfluidics systems allow co-cultures of neurons and different cell types in their appropriate culture media. We have recently demonstrated that trigeminal ganglia (TG) and teeth are able to survive for a long period of time when co-cultured in microfluidic devices, and that they maintain in these conditions the same innervation pattern that they show in vivo. On this basis, we describe how to isolate and co-culture developing trigeminal ganglia and tooth germs in a microfluidic co-culture system.This protocol describes a simple and flexible way to co-culture ganglia/nerves and target tissues and to study the roles of specific molecules on such interactions in a controlled and isolated environment.
神经支配在器官和组织的发育、稳态及再生过程中发挥着关键作用。然而,这些现象背后的机制尚未得到充分理解。特别是,神经支配在牙齿发育和再生中的作用被忽视了。多项体内研究提供了关于各种动物模型发育和修复过程中牙齿组织神经支配模式的重要信息。然而,这些方法大多并非最适合突出神经纤维与靶器官和组织之间相互作用的分子基础。共培养是在可控且隔离的环境中研究和操纵神经纤维与牙齿之间相互作用的一种有价值的方法。在过去几十年里,使用相同培养基的传统共培养仅进行了很短的时间(例如,两天),以研究发育中的口腔和牙齿组织对感觉神经纤维的吸引或排斥作用。然而,需要延长培养时间来研究神经支配对牙齿形态发生和细胞分化的影响。微流控系统允许在合适的培养基中对神经元和不同细胞类型进行共培养。我们最近证明,三叉神经节(TG)和牙齿在微流控装置中共培养时能够长时间存活,并且在这些条件下它们保持与体内相同的神经支配模式。在此基础上,我们描述了如何在微流控共培养系统中分离并共培养发育中的三叉神经节和牙胚。本方案描述了一种简单且灵活的方法,用于共培养神经节/神经和靶组织,并在可控且隔离的环境中研究特定分子在这种相互作用中的作用。