<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><submitter>Mulholland HN</submitter><funding>NEI NIH HHS</funding><funding>NIMH NIH HHS</funding><pubmed_abstract>During development, cortical activity is organized into distributed modular patterns that are a precursor of the mature columnar functional architecture. Theoretically, such structured neural activity can emerge dynamically from local synaptic interactions through a recurrent network with effective local excitation with lateral inhibition (LE/LI) connectivity. Utilizing simultaneous widefield calcium imaging and optogenetics in juvenile ferret cortex prior to eye opening, we directly test several critical predictions of an LE/LI mechanism. We show that cortical networks transform uniform stimulations into diverse modular patterns exhibiting a characteristic spatial wavelength. Moreover, patterned optogenetic stimulation matching this wavelength selectively biases evoked activity patterns, </pubmed_abstract><journal>bioRxiv : the preprint server for biology</journal><pagination>2024.03.02.583133</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10925298</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Self-organization of modular activity in immature cortical networks.</pubmed_title><pmcid>PMC10925298</pmcid><funding_grant_id>R01 EY030893</funding_grant_id><funding_grant_id>F32 MH115688</funding_grant_id><pubmed_authors>Smith GB</pubmed_authors><pubmed_authors>Mulholland HN</pubmed_authors><pubmed_authors>Kaschube M</pubmed_authors></additional><is_claimable>false</is_claimable><name>Self-organization of modular activity in immature cortical networks.</name><description>During development, cortical activity is organized into distributed modular patterns that are a precursor of the mature columnar functional architecture. Theoretically, such structured neural activity can emerge dynamically from local synaptic interactions through a recurrent network with effective local excitation with lateral inhibition (LE/LI) connectivity. Utilizing simultaneous widefield calcium imaging and optogenetics in juvenile ferret cortex prior to eye opening, we directly test several critical predictions of an LE/LI mechanism. We show that cortical networks transform uniform stimulations into diverse modular patterns exhibiting a characteristic spatial wavelength. Moreover, patterned optogenetic stimulation matching this wavelength selectively biases evoked activity patterns, </description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Mar</publication><modification>2025-04-05T13:58:09.712Z</modification><creation>2025-04-05T13:58:09.712Z</creation></dates><accession>S-EPMC10925298</accession><cross_references><pubmed>38464130</pubmed><doi>10.1101/2024.03.02.583133</doi></cross_references></HashMap>