Neocortical activity is stimulus- and scale-invariant
Mounting evidence supports the hypothesis that the cortex operates near a critical state, defined as the transition point between order (large-scale activity) and disorder (small-scale activity). This criticality is manifested by power law distribution of the size and duration of spontaneous cascade...
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description | Mounting evidence supports the hypothesis that the cortex operates near a critical state, defined as the transition point between order (large-scale activity) and disorder (small-scale activity). This criticality is manifested by power law distribution of the size and duration of spontaneous cascades of activity, which are referred as neuronal avalanches. The existence of such neuronal avalanches has been confirmed by several studies both in vitro and in vivo, among different species and across multiple spatial scales. However, despite the prevalence of scale free activity, still very little is known concerning whether and how the scale-free nature of cortical activity is altered during external stimulation. To address this question, we performed in vivo two-photon population calcium imaging of layer 2/3 neurons in primary visual cortex of behaving mice during visual stimulation and conducted statistical analyses on the inferred spike trains. Our investigation for each mouse and condition revealed power law distributed neuronal avalanches, and irregular spiking individual neurons. Importantly, both the avalanche and the spike train properties remained largely unchanged for different stimuli, while the cross-correlation structure varied with stimuli. Our results establish that microcircuits in the visual cortex operate near the critical regime, while rearranging functional connectivity in response to varying sensory inputs. |
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This criticality is manifested by power law distribution of the size and duration of spontaneous cascades of activity, which are referred as neuronal avalanches. The existence of such neuronal avalanches has been confirmed by several studies both in vitro and in vivo, among different species and across multiple spatial scales. However, despite the prevalence of scale free activity, still very little is known concerning whether and how the scale-free nature of cortical activity is altered during external stimulation. To address this question, we performed in vivo two-photon population calcium imaging of layer 2/3 neurons in primary visual cortex of behaving mice during visual stimulation and conducted statistical analyses on the inferred spike trains. Our investigation for each mouse and condition revealed power law distributed neuronal avalanches, and irregular spiking individual neurons. Importantly, both the avalanche and the spike train properties remained largely unchanged for different stimuli, while the cross-correlation structure varied with stimuli. Our results establish that microcircuits in the visual cortex operate near the critical regime, while rearranging functional connectivity in response to varying sensory inputs.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0177396</identifier><identifier>PMID: 28489906</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Action Potentials ; Analysis ; Animals ; Avalanches ; Biology and Life Sciences ; Brain ; Calcium ; Calcium - analysis ; Calcium - metabolism ; Calcium imaging ; Cascades ; Computer and Information Sciences ; Cortex (somatosensory) ; Engineering and Technology ; Experiments ; Firing pattern ; In vitro methods and tests ; In vivo methods and tests ; Laboratory animals ; Landslides ; Medicine and Health Sciences ; Mice, Inbred C57BL ; Models, Neurological ; Neocortex ; Neocortex - cytology ; Neocortex - physiology ; Nerve Net - cytology ; Nerve Net - physiology ; Nervous system ; Neural networks ; Neuroimaging ; Neurons ; Neurons - cytology ; Neurons - physiology ; Neurosciences ; Pain ; Photic Stimulation ; Physics ; Population (statistical) ; Power law ; Rodents ; Science ; Small scale ; Social Sciences ; Spatial distribution ; Statistical analysis ; Stimulation ; Surgery ; Visual cortex ; Visual Cortex - cytology ; Visual Cortex - physiology ; Visual perception ; Visual stimuli</subject><ispartof>PloS one, 2017-05, Vol.12 (5), p.e0177396</ispartof><rights>COPYRIGHT 2017 Public Library of Science</rights><rights>2017 Karimipanah et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2017 Karimipanah et al 2017 Karimipanah et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c692t-20973bb0f4c33c7a8f5c73a5785798ee358fbb80e3fa02bbcc0d365f167bb16a3</citedby><cites>FETCH-LOGICAL-c692t-20973bb0f4c33c7a8f5c73a5785798ee358fbb80e3fa02bbcc0d365f167bb16a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5425225/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5425225/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,315,728,781,785,865,886,2103,2929,23871,27929,27930,53796,53798</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28489906$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Zochowski, Michal</contributor><creatorcontrib>Karimipanah, Yahya</creatorcontrib><creatorcontrib>Ma, Zhengyu</creatorcontrib><creatorcontrib>Miller, Jae-Eun Kang</creatorcontrib><creatorcontrib>Yuste, Rafael</creatorcontrib><creatorcontrib>Wessel, Ralf</creatorcontrib><title>Neocortical activity is stimulus- and scale-invariant</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>Mounting evidence supports the hypothesis that the cortex operates near a critical state, defined as the transition point between order (large-scale activity) and disorder (small-scale activity). 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Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Karimipanah, Yahya</au><au>Ma, Zhengyu</au><au>Miller, Jae-Eun Kang</au><au>Yuste, Rafael</au><au>Wessel, Ralf</au><au>Zochowski, Michal</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Neocortical activity is stimulus- and scale-invariant</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2017-05-10</date><risdate>2017</risdate><volume>12</volume><issue>5</issue><spage>e0177396</spage><pages>e0177396-</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>Mounting evidence supports the hypothesis that the cortex operates near a critical state, defined as the transition point between order (large-scale activity) and disorder (small-scale activity). This criticality is manifested by power law distribution of the size and duration of spontaneous cascades of activity, which are referred as neuronal avalanches. The existence of such neuronal avalanches has been confirmed by several studies both in vitro and in vivo, among different species and across multiple spatial scales. However, despite the prevalence of scale free activity, still very little is known concerning whether and how the scale-free nature of cortical activity is altered during external stimulation. To address this question, we performed in vivo two-photon population calcium imaging of layer 2/3 neurons in primary visual cortex of behaving mice during visual stimulation and conducted statistical analyses on the inferred spike trains. Our investigation for each mouse and condition revealed power law distributed neuronal avalanches, and irregular spiking individual neurons. 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subjects | Action Potentials Analysis Animals Avalanches Biology and Life Sciences Brain Calcium Calcium - analysis Calcium - metabolism Calcium imaging Cascades Computer and Information Sciences Cortex (somatosensory) Engineering and Technology Experiments Firing pattern In vitro methods and tests In vivo methods and tests Laboratory animals Landslides Medicine and Health Sciences Mice, Inbred C57BL Models, Neurological Neocortex Neocortex - cytology Neocortex - physiology Nerve Net - cytology Nerve Net - physiology Nervous system Neural networks Neuroimaging Neurons Neurons - cytology Neurons - physiology Neurosciences Pain Photic Stimulation Physics Population (statistical) Power law Rodents Science Small scale Social Sciences Spatial distribution Statistical analysis Stimulation Surgery Visual cortex Visual Cortex - cytology Visual Cortex - physiology Visual perception Visual stimuli |
title | Neocortical activity is stimulus- and scale-invariant |
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