Acute brain slice methods for adult and aging animals: application of targeted patch clampanalysis and optogenetics
By J. Ting, T. Daigle, Qian Chen, G. Feng. Methods in molecular biology, 2014
617 citations recorded by the source corpus.
Summary The development of the living acute brain slice preparation for analyzing synaptic function roughly a half century ago was a pivotal achievement that greatly influenced the landscape of modern neuroscience. Indeed, many neuroscientists regard brain slices as the gold-standard model system for detailed cellular, molecular, and circuitry level analysis and perturbation of neuronal function. A critical limitation of this model system is the difficulty in preparing slices from adult and aging animals, and over the past several decades few substantial methodological improvements have emerged to facilitate patch clamp analysis in the mature adult stage. In this chapter we describe a robust and practical protocol for preparing brain slices from mature adult mice that are suitable for patch clamp analysis. This method reduces swelling and damage in superficial layers of the slices and improves the success rate for targeted patch clamp recordings, including recordings from fluorescently labeled populations in slices derived from transgenic mice. This adult brain slice method is suitable for diverse experimental applications, including both monitoring and manipulating neuronal activity with genetically encoded calcium indicators and optogenetic actuators, respectively. We describe the application of this adult brain slice platform and associated methods for screening kinetic properties of Channelrhodopsin (ChR) variants expressed in genetically-defined neuronal subtypes.
Subfields: Cellular and Molecular Neuroscience
View Paper: https://www.semanticscholar.org/paper/321510beea8fc90bd5517f83779bdd3a68649e6b
Citations in the corpus
- A suite of transgenic driver and reporter mouse lines with enhanced brain cell type targeting and functionality (2018, neutral): “, 2014) and oChIEF (Ting et al., 2014), new genetically encoded voltage indicator ASAP2s (Chamberland et al.”