{"id":594,"date":"2012-05-10T21:24:45","date_gmt":"2012-05-10T21:24:45","guid":{"rendered":"https:\/\/blogs.nature.com\/actionpotential\/?p=594"},"modified":"2012-05-10T21:28:22","modified_gmt":"2012-05-10T21:28:22","slug":"there_is_no_spoon","status":"publish","type":"post","link":"https:\/\/blogs.nature.com\/actionpotential\/2012\/05\/there_is_no_spoon.html","title":{"rendered":"&#8220;There is no spoon&#8230;&#8221;: Paralyzed fish navigates virtual environment while we watch its brain"},"content":{"rendered":"<div id=\"attachment_597\" style=\"width: 630px\" class=\"wp-caption aligncenter\"><a class=\"wpn-image-link\" href=\"https:\/\/blogs.nature.com\/actionpotential\/files\/2012\/05\/192182_3_supp_1625154_m0fssn.png\"><img loading=\"lazy\" decoding=\"async\" aria-describedby=\"caption-attachment-597\" class=\"size-large wp-image-597 wpn-image\" title=\"192182_3_supp_1625154_m0fssn\" src=\"https:\/\/blogs.nature.com\/actionpotential\/files\/2012\/05\/192182_3_supp_1625154_m0fssn-791x1024.png\" alt=\"\" width=\"620\" height=\"802\" srcset=\"https:\/\/blogs.nature.com\/actionpotential\/files\/2012\/05\/192182_3_supp_1625154_m0fssn-791x1024.png 791w, https:\/\/blogs.nature.com\/actionpotential\/files\/2012\/05\/192182_3_supp_1625154_m0fssn-231x300.png 231w\" sizes=\"auto, (max-width: 620px) 100vw, 620px\" \/><\/a><p id=\"caption-attachment-597\" class=\"wp-caption-text\">Overlaid on the micrograph of the fish is a slice of its brain measured with a laser scanning microscope, in which single neurons are visible.{credit}(courtesy of Ahrens et al.){\/credit}<\/p><\/div>\n<p>Sometimes an experiment will just reach off the page and slap you in the face, demanding attention. This happens to me every so often and I must admit, our latest paper from the lab of <a href=\"https:\/\/www.mcb.harvard.edu\/Engert\/\" target=\"_blank\">Florien Engert<\/a> induced such an experience. There have been several cool, technical tours-de-force (is that proper grammar??) over the last few years involving different creatures navigating in a virtual environment while neuronal activity was monitored. These include <a href=\"https:\/\/www.nature.com\/nature\/journal\/v461\/n7266\/abs\/nature08499.html\" target=\"_blank\">a mouse running on a spherical treadmill<\/a>, as well as <a href=\"https:\/\/www.nature.com\/nmeth\/journal\/v7\/n7\/full\/nmeth.1468.html\" target=\"_blank\">a fly marching along a similar treadmill-style ball<\/a>. But in these examples, having the subject head-fixed (for the stability of recordings in the brain, either with electrodes or through imaging) was moderately non-intrusive since walking motions were independent of the head. The same can&#8217;t be said for the subject in this latest example of a virtual reality navigator: a wriggling, swimming fish. Therefore, a more creative solution had to be sought and <a href=\"https:\/\/www.nature.com\/nature\/journal\/vaop\/ncurrent\/full\/nature11057.html\" target=\"_blank\">in a paper published online yesterday<\/a>, Ahrens, Engert and colleagues decided that paralysis was the way to go in order to follow the neural activity of this navigating fish.<!--more--><\/p>\n<p>Zebrafish have long been used as a model system for a variety of experiments, but motor control long been at the forefront of topics. They offer many distinct advantages over mammalian-based systems, including the genetic tractability of <em>Drosophila<\/em> and the ease with which microscopy methods can be utilized; larval zebrafish are transparent, so no surgery is required in order to open up a &#8220;window&#8221; for fluorescence imaging. And more recently, several labs have begun to develop rich behavioral methods to further explore the limits of probing functional circuitry in these beasts. So what was interesting and cool about this latest fish-based technology? From the authors, here is the system set-up:<\/p>\n<blockquote><p><em>To examine neural dynamics across brain areas that drive sensorimotor recalibration, we developed a system to study neural activity at cellular resolution<sup><a id=\"ref-link-20\" title=\"Gahtan, E., Sankrithi, N., Campos, J. B. &amp; O\/'Malley, D. M. Evidence for a widespread brain stem escape network in larval zebrafish. J. Neurophysiol. 87, 608-614 (2002)\" href=\"https:\/\/www.nature.com\/nature\/journal\/vaop\/ncurrent\/full\/nature11057.html#ref17\">17<\/a>, <a id=\"ref-link-21\" title=\"Ohki, K., Chung, S., Ch\/'ng, Y. H., Kara, P. &amp; Reid, R. C. Functional imaging with cellular resolution reveals precise micro-architecture in visual cortex. Nature 433, 597-603 (2005)\" href=\"https:\/\/www.nature.com\/nature\/journal\/vaop\/ncurrent\/full\/nature11057.html#ref18\">18<\/a><\/sup>, using two-photon microscopy<sup><a id=\"ref-link-22\" title=\"Denk, W., Strickler, J. H. &amp; Webb, W. W. Two-photon laser scanning fluorescence microscopy. Science 248, 73-76 (1990)\" href=\"https:\/\/www.nature.com\/nature\/journal\/vaop\/ncurrent\/full\/nature11057.html#ref19\">19<\/a><\/sup>, anywhere in the brain<sup><a id=\"ref-link-23\" title=\"Higashijima, S.-I., Masino, M. A., Mandel, G. &amp; Fetcho, J. R. Imaging neuronal activity during zebrafish behavior with a genetically encoded calcium indicator. J. Neurophysiol. 90, 3986-3997 (2003)\" href=\"https:\/\/www.nature.com\/nature\/journal\/vaop\/ncurrent\/full\/nature11057.html#ref20\">20<\/a><\/sup> during closed-loop optomotor behaviour in larval zebrafish. These animals have a small and transparent brain that is readily accessible for optogenetic recording and stimulation<sup><a id=\"ref-link-24\" title=\"Bene, F. D. et al. Filtering of visual information in the tectum by an identified neural circuit. Science 330, 669-673 (2010)\" href=\"https:\/\/www.nature.com\/nature\/journal\/vaop\/ncurrent\/full\/nature11057.html#ref21\">21<\/a>, <a id=\"ref-link-25\" title=\"Douglass, A. D., Kraves, S., Deisseroth, K., Schier, A. F. &amp; Engert, F. Escape behavior elicited by single, channelrhodopsin-2-evoked spikes in zebrafish somatosensory neurons. Curr. Biol. 18, 1133-1137 (2008)\" href=\"https:\/\/www.nature.com\/nature\/journal\/vaop\/ncurrent\/full\/nature11057.html#ref22\">22<\/a><\/sup>, electrophysiology<sup><a id=\"ref-link-26\" title=\"Chong, M. and Drapeau, P. Interaction between hindbrain and spinal networks during the development of locomotion in zebrafish. Dev. Neurobiol. 67, 933-947 (2007)\" href=\"https:\/\/www.nature.com\/nature\/journal\/vaop\/ncurrent\/full\/nature11057.html#ref23\">23<\/a><\/sup> and single-cell ablation<sup><a id=\"ref-link-27\" title=\"Orger, M. B., Kampff, A. R., Severi, K. E., Bollmann, J. H. &amp; Engert, F. Control of visually guided behavior by distinct populations of spinal projection neurons. Nature Neurosci. 11, 327-333 (2008)\" href=\"https:\/\/www.nature.com\/nature\/journal\/vaop\/ncurrent\/full\/nature11057.html#ref24\">24<\/a><\/sup>. To remove motion artefacts<sup><a id=\"ref-link-28\" title=\"O\/'Malley, D. M., Kao, Y. H. &amp; Fetcho, J. R. Imaging the functional organization of zebrafish hindbrain segments during escape behaviors. Neuron 17, 1145-1155 (1996)\" href=\"https:\/\/www.nature.com\/nature\/journal\/vaop\/ncurrent\/full\/nature11057.html#ref25\">25<\/a>, <a id=\"ref-link-29\" title=\"Dombeck, D. A., Khabbaz, A. N., Collman, F., Adelman, T. L. &amp; Tank, D. W. Imaging large-scale neural activity with cellular resolution in awake, mobile mice. Neuron 56, 43-57 (2007)\" href=\"https:\/\/www.nature.com\/nature\/journal\/vaop\/ncurrent\/full\/nature11057.html#ref26\">26<\/a><\/sup>, we developed a swim simulator for completely paralysed larvae (<a href=\"https:\/\/www.nature.com\/nature\/journal\/vaop\/ncurrent\/full\/nature11057.html#f1\">Fig. 1a<\/a>). Motor commands, or \u2018fictive swims\u2019, are recorded at the motor neuron level<sup><a id=\"ref-link-30\" title=\"Mohl, B. Short-term learning during flight control in Locusta migratoria. J. Comp. Physiol. 163, 803-812 (1988)\" href=\"https:\/\/www.nature.com\/nature\/journal\/vaop\/ncurrent\/full\/nature11057.html#ref8\">8<\/a>, <a id=\"ref-link-31\" title=\"Masino, M. A. &amp; Fetcho, J. R. Fictive swimming motor patterns in wild type and mutant larval zebrafish. J. Neurophysiol. 93, 3177-3188 (2005)\" href=\"https:\/\/www.nature.com\/nature\/journal\/vaop\/ncurrent\/full\/nature11057.html#ref27\">27<\/a>, <a id=\"ref-link-32\" title=\"Cohen, A. H. &amp; Wallen, P. The neuronal correlate of locomotion in fish. [ldquo]fictive swimming[rdquo] induced in an in vitro preparation of the lamprey spinal cord. Exp. Brain Res. 41, 11-18 (1980)\" href=\"https:\/\/www.nature.com\/nature\/journal\/vaop\/ncurrent\/full\/nature11057.html#ref28\">28<\/a><\/sup> (<a href=\"https:\/\/www.nature.com\/nature\/journal\/vaop\/ncurrent\/full\/nature11057.html#f1\">Fig. 1c, d<\/a>) and translated, in real time, into visual feedback that resembles the optic flow of freely swimming fish (Methods). This constitutes a fictively driven virtual-reality setup. Simultaneously, a two-photon microscope scanning over a transgenic fish expressing GCaMP2 (ref. <a id=\"ref-link-33\" title=\"Tallini, Y. N. et al. Imaging cellular signals in the heart in vivo: cardiac expression of the high-signal Ca2+ indicator GCaMP2. Proc. Natl Acad. Sci. USA 103, 4753-4758 (2006)\" href=\"https:\/\/www.nature.com\/nature\/journal\/vaop\/ncurrent\/full\/nature11057.html#ref29\">29<\/a>) in almost all neurons<sup><a id=\"ref-link-34\" title=\"Higashijima, S.-I., Masino, M. A., Mandel, G. &amp; Fetcho, J. R. Imaging neuronal activity during zebrafish behavior with a genetically encoded calcium indicator. J. Neurophysiol. 90, 3986-3997 (2003)\" href=\"https:\/\/www.nature.com\/nature\/journal\/vaop\/ncurrent\/full\/nature11057.html#ref20\">20<\/a>, <a id=\"ref-link-35\" title=\"Park, H. C. et al. Analysis of upstream elements in the HuC promoter leads to the establishment of transgenic zebrafish with fluorescent neurons. Dev. Biol. 227, 279-293 (2000)\" href=\"https:\/\/www.nature.com\/nature\/journal\/vaop\/ncurrent\/full\/nature11057.html#ref30\">30<\/a><\/sup> allows activity to be monitored throughout the brain at single-neuron resolution. As the experimenter is in complete control of the visual feedback, this allowed us to study neural dynamics during visually guided motor adaptation throughout the brain at the cellular level.<\/em><\/p><\/blockquote>\n<p>Allow me to translate: &#8220;WE CREATED &#8220;<em>THE MATRIX<\/em>&#8221; FOR FISH.<\/p>\n<p>Using this system, the authors were able to break down neural response properties during behavioral adaptation to perturbations in the virtual environment into four different categories, and the excellent spatial resolution of this technique allowed them to accurately map the anatomical substrate for each response. Some of these responses were observed while the fish was progressing through behavioral adjustments to the stimulus provided in the virtual world, strongly suggesting that focus on these elements could potentially yield functional insights into adaptive motor learning. Indeed, laser-based lesioning of one identified site, the inferior olive, did negatively affect visually-induced motor adaptation learning. Therefore, the authors had identified a powerful model for the study of brain-wide activity during adaptive locomotion.<\/p>\n<p>The reviews for this paper were quite positive with regards to the innovative technology and each easily recognized the potential for this system, but the original version of the manuscript failed to provide a &#8220;proof-of-principle&#8221; for its utility; i.e., demonstrating novel insights into motor adaptation programs. Two referees even had concerns that there was a novelty issue when comparing this system to other virtual reality set-ups, including those mentioned earlier. At <em>Nature<\/em>, we aren&#8217;t shy about publishing manuscripts that are wholly-focused on technology and innovation, but in this particular case, although I was dazzled by the technique, we needed to go a little deeper into the biology in order to differentiate this system from the others and demonstrate its power. One could potentially make the argument that working in zebrafish is not as common as working in mammals or even insects, so if this paper was to be significant for a very broad audience, we had to throw some biology at the reader, in addition to the cool kit.<\/p>\n<p>The authors graciously agreed to explore the circuitry further, adding new experiments to test the role and functionality of some of the neural response properties they observed. It took some time to get everything right, but in the end, both editors and (most) reviewers were satisfied that this paper had reached a point where it was not only showcasing the methodology, but also providing some novel biological insights. I say &#8220;most&#8221; because as is the case often times, not all reviewers were on board with the changes. In a rare occurrence, one reviewer was strongly supportive of publication in the initial round, with this existing more as a methods paper, but soured as the paper became more complex. The &#8220;biological insight&#8221; observations and extra modeling were not as graciously received, with this reviewer feeling these parts detracted from the rest of the paper. It&#8217;s not that this referee undervalues biological insight, rather the main concern was that the new insights require greater development and more sophisticated manipulation beyond lesion-based experiments to provide real value (one can imagine the power of working optogenetics into this set-up.) Fair enough, but in the end we felt the manuscript benefited from this brief, natural extension, to best-demonstrate the power of an exciting new system. Feel free to disagree with this editorial decision in the comments.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Sometimes an experiment will just reach off the page and slap you in the face, demanding attention. This happens to me every so often and I must admit, our latest paper from the lab of Florien Engert induced such an experience. There have been several cool, technical tours-de-force (is that proper grammar??) over the last few years involving different creatures navigating in a virtual environment while neuronal activity was monitored. These include a mouse running on a spherical treadmill, as well as a fly marching along a similar treadmill-style ball. But in these examples, having the subject head-fixed (for the stability of recordings in the brain, either with electrodes or through imaging) was moderately non-intrusive since walking motions were independent of the head. The same can\u2019t be said for the subject in this latest example of a virtual reality navigator: a wriggling, swimming fish. Therefore, a more creative solution had to be sought and in a paper published online yesterday, Ahrens, Engert and colleagues decided that paralysis was the way to go in order to follow the neural activity of this navigating fish.&nbsp; <a href=\"https:\/\/blogs.nature.com\/actionpotential\/2012\/05\/there_is_no_spoon.html#wpn-more-594\" class=\"more-link\">Read more<\/a> <a href=\"https:\/\/blogs.nature.com\/actionpotential\/2012\/05\/there_is_no_spoon.html\">Continue reading <span class=\"meta-nav\">&rarr;<\/span><\/a><\/p>\n","protected":false},"author":89,"featured_media":0,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[18,4],"tags":[62,61,23,34,47,19,60,44,41,28,20,59,58],"class_list":["post-594","post","type-post","status-publish","format-standard","hentry","category-new-in-nature","category-noah-gray","tag-adaptation","tag-calcium-imaging","tag-cerebellum","tag-decoding","tag-motor-learning","tag-nature","tag-navigation","tag-neural-circuits","tag-neural-plasticity","tag-neurons","tag-neuroscience","tag-virtual-reality","tag-zebrafish"],"_links":{"self":[{"href":"https:\/\/blogs.nature.com\/actionpotential\/wp-json\/wp\/v2\/posts\/594","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/blogs.nature.com\/actionpotential\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/blogs.nature.com\/actionpotential\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/blogs.nature.com\/actionpotential\/wp-json\/wp\/v2\/users\/89"}],"replies":[{"embeddable":true,"href":"https:\/\/blogs.nature.com\/actionpotential\/wp-json\/wp\/v2\/comments?post=594"}],"version-history":[{"count":0,"href":"https:\/\/blogs.nature.com\/actionpotential\/wp-json\/wp\/v2\/posts\/594\/revisions"}],"wp:attachment":[{"href":"https:\/\/blogs.nature.com\/actionpotential\/wp-json\/wp\/v2\/media?parent=594"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/blogs.nature.com\/actionpotential\/wp-json\/wp\/v2\/categories?post=594"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/blogs.nature.com\/actionpotential\/wp-json\/wp\/v2\/tags?post=594"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}