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Optical Imaging of Neocortical Dynamics PDF

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Neuromethods 85 Bruno Weber Fritjof Helmchen Editors Optical Imaging of Neocortical Dynamics N EUROMETHODS Series Editor Wolfgang Walz University of Saskatchewan Saskatoon, SK, Canada For further volumes: h ttp://www.springer.com/series/7657 Optical Imaging of Neocortical Dynamics Edited by Bruno Weber Institute of Pharmacology and Toxicology, University of Zurich, Zurich, Switzerland Fritjof H elmchen Brain Research Institute, University of Zurich, Zurich, Switzerland Editors Bruno W eber Fritjof H elmchen Institute of Pharmacology and Toxicology Brain Research Institute University of Zurich University of Zurich Zurich , S witzerland Zurich, Switzerland ISSN 0893-2336 ISSN 1940-6045 (electronic) ISBN 978-1-62703-784-6 ISBN 978-1-62703-785-3 (eBook) DOI 10.1007/978-1-62703-785-3 Springer New York Heidelberg Dordrecht London Library of Congress Control Number: 2013957690 © Springer Science+Business Media New York 2 014 This work is subject to copyright. All rights are reserved by the Publisher, whether the whole or part of the material is concerned, specifi cally the rights of translation, reprinting, reuse of illustrations, recitation, broadcasting, reproduction on microfi lms or in any other physical way, and transmission or information storage and retrieval, electronic adaptation, computer software, or by similar or dissimilar methodology now known or hereafter developed. Exempted from this legal reservation are brief excerpts in connection with reviews or scholarly analysis or material supplied specifi cally for the purpose of being entered and executed on a computer system, for exclusive use by the purchaser of the work. Duplication of this publication or parts thereof is permitted only under the provisions of the Copyright Law of the Publisher’s location, in its current version, and permission for use must always be obtained from Springer. Permissions for use may be obtained through RightsLink at the Copyright Clearance Center. Violations are liable to prosecution under the respective Copyright Law. The use of general descriptive names, registered names, trademarks, service marks, etc. in this publication does not imply, even in the absence of a specifi c statement, that such names are exempt from the relevant protective laws and regulations and therefore free for general use. While the advice and information in this book are believed to be true and accurate at the date of publication, neither the authors nor the editors nor the publisher can accept any legal responsibility for any errors or omissions that may be made. The publisher makes no warranty, express or implied, with respect to the material contained herein. Printed on acid-free paper Humana Press is a brand of Springer Springer is part of Springer Science+Business Media (www.springer.com) Series P reface Under the guidance of its founders Alan Boulton and Glen Baker, the Neuromethods series by Humana Press has been very successful since the fi rst volume appeared in 1985. In about 17 years, 37 volumes have been published. In 2006, Springer Science + Business Media made a renewed commitment to this series. The new program will focus on methods that are either unique to the nervous system and excitable cells or which need special consideration to be applied to the neurosciences. The program will strike a balance between recent and exciting developments like those concerning new animal models of disease, imaging, in vivo methods, and more established techniques. These include immunocytochemistry and elec- trophysiological technologies. New trainees in neurosciences still need a sound footing in these older methods in order to apply a critical approach to their results. The careful applica- tion of methods is probably the most important step in the process of scientifi c inquiry. In the past, new methodologies led the way in developing new disciplines in the biological and medical sciences. For example, Physiology emerged out of Anatomy in the nineteenth cen- tury by harnessing new methods based on the newly discovered phenomenon of electricity. Nowadays, the relationships between disciplines and methods are more complex. Methods are now widely shared between disciplines and research areas. New developments in elec- tronic publishing also make it possible for scientists to download chapters or protocols selec- tively within a very short time of encountering them. This new approach has been taken into account in the design of individual volumes and chapters in this series. Saskatoon, SK, Canada Wolfgang Walz v Prefa ce Optical methods for functional imaging are indispensible tools for modern neuroscience due to their exceptional spatial and temporal sampling options and the large variety of pos- sible functional read-outs ranging from voltage changes to metabolic states. As such, state- of-the-art optical imaging techniques have emerged as pivotal approaches for advancing our understanding of information processing in the mammalian neocortex, and many of the most imperative issues have now become technically accessible. The main goal of the present volume is to provide a collection of the most relevant optical methods currently used for investigating neocortical circuit dynamics. We believe that we were able to share our enthusiasm for this endeavor with a group of outstanding authors who have been instrumental in advancing optical methods in the past years and who at the same time are very successful users of those methods for interrogating the neocortex. We hope that the volume is useful for students as well as neuroscientists interested in applying optical approaches to answer their specifi c questions. The wealth of optical imaging methods that are currently applied in the neurosciences has forced us to limit the range to methods that (1) are applied in experiments in vivo, mainly in the rodent brain, and (2) measure the functional properties on the spatial scale of cortical circuits. We have divided the volume into three parts: Part I is an introductory section that covers the physical fundamentals of optical i maging and introduces the molecular tools and imaging devices used for in vivo optical imaging. The fi rst chapter outlines the methodological concepts of using light to address current questions in neuroscience. Next, two chapters treat the physical principles of imaging and the optical properties of brain tissue, respectively, followed by two further chapters that introduce functional indicators as well as light-controllable molecules. These fi ve chapters thus provide a background for all the chapters in P arts II and III . Part II covers the most relevant methods and their applications to investigate neuronal activity in the neocortex across a wide range of spatial and temporal scales. Several chapters present the advantages of two-photon microscopy to study neocortical dynamics, largely using in vivo calcium imaging from individual neurons and their dendrites or from large neuronal populations. Wide-fi eld voltage-sensitive dye imaging is demonstrated as a com- plementary technique to reveal large-scale dynamics. In addition, the opportunities to probe causal relationship between cellular and circuit mechanisms and behavior with opto- genetic tools are explained. Part III focuses on optical imaging methods used to probe signals that do not directly refl ect neuronal activity but provide information on the metabolic state of the cortex. The fi rst two chapters address methods for imaging signals that originate from astrocytes and microglia. The remaining three chapters introduce techniques for measuring hemodynam- ics as well as oxygenation of blood and tissue. vii viii Preface Optical imaging is one of the most dynamic technological fi elds in neuroscience. Novel techniques, such as new optical probes or imaging instruments, are continually emerging and published in the most prestigious journals. In a way, this ever-changing fi eld is thus very diffi cult to capture in a methods book, because the moment it is produced, the tech- nological landscape may have changed again signifi cantly. We nevertheless hope that our collection is useful even in the light of rapid changes, in part because some of the funda- mental concepts remain unchanged. Our main thanks go to all the authors for their outstanding contributions to this vol- ume. We would also like to thank Michaela Thallmair and Ladan Egolf for their editorial assistance. Zürich , S witzerland Bruno Weber Fritjof Helmchen Contents Series Preface . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . v Preface. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . vii Contributors. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . xi PART I F UNDAMENTALS OF USING LIGHT TO STUDY NEOCORTICAL DYNAMICS 1 Neocortex in the Spotlight: Concepts, Questions, and Methods . . . . . . . . . . . 3 Fritjof Helmchen and Bruno Weber 2 Principles and Fundamentals of Optical Imaging. . . . . . . . . . . . . . . . . . . . . . . 19 Frank Scheffold 3 Optical Properties of Neural Tissue. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 33 Andrew K. Dunn 4 Fluorescent Indicators for Functional Optical Imaging . . . . . . . . . . . . . . . . . . 53 Walther Akemann, Hiroki Mutoh, and Thomas Knöpfel 5 Optogenetic Tools for Control of Neural Activity . . . . . . . . . . . . . . . . . . . . . . 73 Lief E. Fenno and Karl Deisseroth PART II SHEDDING LIGHT ON CORTICAL ACTIVITY STATES 6 In Vivo Dendritic Mapping of Sensory Inputs in Cortical Neurons . . . . . . . . . 89 Hongbo Jia and Arthur Konnerth 7 In Vivo Population Imaging of Dendritic Integration in Neocortex. . . . . . . . . 107 Masanori Murayama and Matthew E. Larkum 8 Voltage-Sensitive Dye Imaging of Cortical Dynamics. . . . . . . . . . . . . . . . . . . . 117 Carl C.H. Petersen 9 Two-Photon Imaging of Neuronal Network Dynamics in Neocortex . . . . . . . 133 Benjamin F. Grewe, Fritjof Helmchen, and Björn M. Kampa 10 Chronic Two-Photon Imaging of Neural Activity in the Anesthetized and Awake Behaving Rodent . . . . . . . . . . . . . . . . . . . . . . 151 David J. Margolis, Henry Lütcke, Fritjof Helmchen, Bruno Weber, and Florent Haiss 11 Neocortical Circuit Interrogation with Optogenetics. . . . . . . . . . . . . . . . . . . . 175 Lief E. Fenno and Karl Deisseroth ix

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