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Actin Grips: Circular Actin-Rich Cytoskeletal Structures that Mediate the Wrapping of Polymeric Microfibers by Endothelial Cells

Interaction of endothelial-lineage cells with three-dimensional substrates was much less studied than that with flat culture surfaces. We investigated the in vitro attachment of both mature endothelial cells (ECs) and of less differentiated EC colony-forming cells to poly-e-capro-lactone (PCL) fiber...

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Autores principales: Jones, Desiree, Park, DoYoung, Anghelina, Mirela, Pecot, Thierry, Machiraju, Raghu, Xue, Ruipeng, Lannutti, John, Thomas, Jessica, Cole, Sara, Moldovan, Leni, Moldovan, Nicanor I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4418805/
https://www.ncbi.nlm.nih.gov/pubmed/25818446
http://dx.doi.org/10.1016/j.biomaterials.2015.02.034
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author Jones, Desiree
Park, DoYoung
Anghelina, Mirela
Pecot, Thierry
Machiraju, Raghu
Xue, Ruipeng
Lannutti, John
Thomas, Jessica
Cole, Sara
Moldovan, Leni
Moldovan, Nicanor I.
author_facet Jones, Desiree
Park, DoYoung
Anghelina, Mirela
Pecot, Thierry
Machiraju, Raghu
Xue, Ruipeng
Lannutti, John
Thomas, Jessica
Cole, Sara
Moldovan, Leni
Moldovan, Nicanor I.
author_sort Jones, Desiree
collection PubMed
description Interaction of endothelial-lineage cells with three-dimensional substrates was much less studied than that with flat culture surfaces. We investigated the in vitro attachment of both mature endothelial cells (ECs) and of less differentiated EC colony-forming cells to poly-e-capro-lactone (PCL) fibers with diameters in 5–20 μm range (‘scaffold microfibers’, SMFs). We found that notwithstanding the poor intrinsic adhesiveness to PCL, both cell types completely wrapped the SMFs after long-term cultivation, thus attaining a cylindrical morphology. In this system, both EC types grew vigorously for more than a week and became increasingly more differentiated, as shown by multiplexed gene expression. Three-dimensional reconstructions from multiphoton confocal microscopy images using custom software showed that the filamentous (F) actin bundles took a conspicuous ring-like organization around the SMFs. Unlike the classical F-actin-containing stress fibers, these rings were not associated with either focal adhesions or intermediate filaments. We also demonstrated that plasma membrane boundaries adjacent to these circular cytoskeletal structures were tightly yet dynamically apposed to the SMFs, for which reason we suggest to call them ‘actin grips’. In conclusion, we describe a particular form of F-actin assembly with relevance for cytoskeletal organization in response to biomaterials, for endothelial-specific cell behavior in vitro and in vivo, and for tissue engineering.
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spelling pubmed-44188052016-06-01 Actin Grips: Circular Actin-Rich Cytoskeletal Structures that Mediate the Wrapping of Polymeric Microfibers by Endothelial Cells Jones, Desiree Park, DoYoung Anghelina, Mirela Pecot, Thierry Machiraju, Raghu Xue, Ruipeng Lannutti, John Thomas, Jessica Cole, Sara Moldovan, Leni Moldovan, Nicanor I. Biomaterials Article Interaction of endothelial-lineage cells with three-dimensional substrates was much less studied than that with flat culture surfaces. We investigated the in vitro attachment of both mature endothelial cells (ECs) and of less differentiated EC colony-forming cells to poly-e-capro-lactone (PCL) fibers with diameters in 5–20 μm range (‘scaffold microfibers’, SMFs). We found that notwithstanding the poor intrinsic adhesiveness to PCL, both cell types completely wrapped the SMFs after long-term cultivation, thus attaining a cylindrical morphology. In this system, both EC types grew vigorously for more than a week and became increasingly more differentiated, as shown by multiplexed gene expression. Three-dimensional reconstructions from multiphoton confocal microscopy images using custom software showed that the filamentous (F) actin bundles took a conspicuous ring-like organization around the SMFs. Unlike the classical F-actin-containing stress fibers, these rings were not associated with either focal adhesions or intermediate filaments. We also demonstrated that plasma membrane boundaries adjacent to these circular cytoskeletal structures were tightly yet dynamically apposed to the SMFs, for which reason we suggest to call them ‘actin grips’. In conclusion, we describe a particular form of F-actin assembly with relevance for cytoskeletal organization in response to biomaterials, for endothelial-specific cell behavior in vitro and in vivo, and for tissue engineering. 2015-03-18 2015-06 /pmc/articles/PMC4418805/ /pubmed/25818446 http://dx.doi.org/10.1016/j.biomaterials.2015.02.034 Text en © 2015 Published by Elsevier Ltd. http://creativecommons.org/licenses/by/4.0/ This manuscript version is made available under the CC BY-NC-ND 4.0 license.
spellingShingle Article
Jones, Desiree
Park, DoYoung
Anghelina, Mirela
Pecot, Thierry
Machiraju, Raghu
Xue, Ruipeng
Lannutti, John
Thomas, Jessica
Cole, Sara
Moldovan, Leni
Moldovan, Nicanor I.
Actin Grips: Circular Actin-Rich Cytoskeletal Structures that Mediate the Wrapping of Polymeric Microfibers by Endothelial Cells
title Actin Grips: Circular Actin-Rich Cytoskeletal Structures that Mediate the Wrapping of Polymeric Microfibers by Endothelial Cells
title_full Actin Grips: Circular Actin-Rich Cytoskeletal Structures that Mediate the Wrapping of Polymeric Microfibers by Endothelial Cells
title_fullStr Actin Grips: Circular Actin-Rich Cytoskeletal Structures that Mediate the Wrapping of Polymeric Microfibers by Endothelial Cells
title_full_unstemmed Actin Grips: Circular Actin-Rich Cytoskeletal Structures that Mediate the Wrapping of Polymeric Microfibers by Endothelial Cells
title_short Actin Grips: Circular Actin-Rich Cytoskeletal Structures that Mediate the Wrapping of Polymeric Microfibers by Endothelial Cells
title_sort actin grips: circular actin-rich cytoskeletal structures that mediate the wrapping of polymeric microfibers by endothelial cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4418805/
https://www.ncbi.nlm.nih.gov/pubmed/25818446
http://dx.doi.org/10.1016/j.biomaterials.2015.02.034
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