Department of Pharmacology and Neuroscience and Mental Health Institute, University of Alberta, Edmonton, Alberta, Canada.
Center for the Neurobiology of Stress Resilience and Psychiatric Disorders, Chicago Medical School/Rosalind Franklin University of Medicine & Science, North Chicago, Illinois.
Curr Protoc. 2021 Oct;1(10):e267. doi: 10.1002/cpz1.267.
Organotypic slice cultures (OTCs) have been employed in the laboratory since the early 1980s and have proved to be useful for the study of a number of neural systems. Our recent work focuses on the development of behavioral stress resilience induced by repeated daily injections of neuropeptide Y into the basolateral amygdala (BLA). Resilience develops over weeks, persisting to 8 weeks. To unravel the cellular mechanisms underlying neuropeptide Y-induced stress resilience we developed in vitro OTCs of the BLA. Here, we provide an optimized protocol that consistently yields viable and healthy OTCs containing the BLA and surrounding tissue using the interface method, prepared with slices taken from postnatal (P) day 14 rats. We explain key points to optimizing tissue viability and discuss mitigation or avoidance of pitfalls that can arise to aid in successful implementation of this technique. We show that principal neurons in BLA OTCs (8 weeks in vitro = equivalent postnatal day 70) develop into networks that are electrophysiologically very similar to those from acute slices obtained from older rats (P70) and respond to pharmacological treatments in a comparable way. Furthermore, we highlight how these cultures be used to further understand the molecular, cellular, and circuit-level neuropathophysiological changes underlying stress disorders. BLA OTCs provide long-term physiological and pharmacological results whose predictions were borne out in vivo, supporting the validity of the BLA OTC as a model to unravel BLA neurocircuitry. Recent preliminary results also support the successful application of this approach to preparing long-lived OTCs of BLA and neocortex from mice. © 2021 Wiley Periodicals LLC. Basic Protocol 1: Organotypic slice culture Support Protocol 1: Changing medium Support Protocol 2: Drug incubations Basic Protocol 2: Excision of OTC slices from inserts Support Protocol 3: Fixation of slices.
器官型脑片培养(OTCs)自 20 世纪 80 年代初以来一直在实验室中使用,并且已被证明对许多神经系统的研究非常有用。我们最近的工作重点是通过在基底外侧杏仁核(BLA)中重复每日注射神经肽 Y 来开发行为应激弹性。弹性在数周内发展,持续到 8 周。为了解开神经肽 Y 诱导的应激弹性的细胞机制,我们开发了体外 BLA 的 OTCs。在这里,我们提供了一个优化的方案,该方案使用界面方法从出生后第 14 天(P)的大鼠中获得的切片,一致地产生包含 BLA 和周围组织的可行且健康的 OTCs。我们解释了优化组织活力的要点,并讨论了减轻或避免可能出现的陷阱的方法,以帮助成功实施该技术。我们表明,BLA OTCs 中的主神经元(8 周龄体外培养相当于出生后第 70 天)发育成电生理上非常类似于从较老大鼠(P70)获得的急性切片的网络,并以类似的方式对药物处理做出反应。此外,我们强调了这些培养物如何用于进一步了解应激障碍的分子、细胞和电路水平神经病理生理学变化。BLA OTCs 提供了长期的生理和药理结果,这些结果在体内得到了验证,支持了 BLA OTC 作为揭示 BLA 神经回路的模型的有效性。最近的初步结果还支持将这种方法成功应用于从小鼠制备长期存活的 BLA 和新皮层 OTCs。