<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Wubshet NH</submitter><funding>NIBIB NIH HHS</funding><funding>National Institutes of Health</funding><funding>NIH HHS</funding><funding>National Science Foundation</funding><pagination>310-317</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11303591</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>81(8)</volume><pubmed_abstract>Although diverse actin network architectures found inside the cell have been individually reconstituted outside of the cell, how different types of actin architectures reorganize under applied forces is not entirely understood. Recently, bottom-up reconstitution has enabled studies where dynamic and phenotypic characteristics of various actin networks can be recreated in an isolated cell-like environment. Here, by creating a giant unilamellar vesicle (GUV)-based cell model encapsulating actin networks, we investigate how actin networks rearrange in response to localized stresses applied by micropipette aspiration. We reconstitute actin bundles and branched bundles in GUVs separately and mechanically perturb them. Interestingly, we find that, when aspirated, protrusive actin bundles that ar</pubmed_abstract><journal>Cytoskeleton (Hoboken, N.J.)</journal><pubmed_title>Rearrangement of GUV-confined actin networks in response to micropipette aspiration.</pubmed_title><pmcid>PMC11303591</pmcid><funding_grant_id>MCB-2201236</funding_grant_id><funding_grant_id>R01 EB030031</funding_grant_id><funding_grant_id>T32 EB005582</funding_grant_id><funding_grant_id>EF1935265</funding_grant_id><funding_grant_id>NIH NIBIB T32 EB005582</funding_grant_id><funding_grant_id>MCB‐2201236</funding_grant_id><pubmed_authors>Wubshet NH</pubmed_authors><pubmed_authors>Liu AP</pubmed_authors><pubmed_authors>Young CJ</pubmed_authors></additional><is_claimable>false</is_claimable><name>Rearrangement of GUV-confined actin networks in response to micropipette aspiration.</name><description>Although diverse actin network architectures found inside the cell have been individually reconstituted outside of the cell, how different types of actin architectures reorganize under applied forces is not entirely understood. Recently, bottom-up reconstitution has enabled studies where dynamic and phenotypic characteristics of various actin networks can be recreated in an isolated cell-like environment. Here, by creating a giant unilamellar vesicle (GUV)-based cell model encapsulating actin networks, we investigate how actin networks rearrange in response to localized stresses applied by micropipette aspiration. We reconstitute actin bundles and branched bundles in GUVs separately and mechanically perturb them. Interestingly, we find that, when aspirated, protrusive actin bundles that ar</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Aug</publication><modification>2026-03-18T13:31:37.784Z</modification><creation>2025-08-18T09:54:03.641Z</creation></dates><accession>S-EPMC11303591</accession><cross_references><pubmed>38326972</pubmed><doi>10.1002/cm.21836</doi></cross_references></HashMap>