Cationic Nanocylinders Promote Angiogenic Activities of Endothelial Cells

Polymers have been used extensively taking forms as scaffolds, patterned surface and nanoparticle for regenerative medicine applications. Angiogenesis is an essential process for successful tissue regeneration, and endothelial cell–cell interaction plays a pivotal role in regulating their tight junc...

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Main Authors: Jung Bok Lee, Daniel A. Balikov, Jae Won Yang, Ki Seok Kim, Hun Kuk Park, Jeong Koo Kim, Il Keun Kwon, Leon M. Bellan, Hak-Joon Sung
Format: Article
Language:English
Published: MDPI AG 2016-01-01
Series:Polymers
Subjects:
Online Access:http://www.mdpi.com/2073-4360/8/1/15
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author Jung Bok Lee
Daniel A. Balikov
Jae Won Yang
Ki Seok Kim
Hun Kuk Park
Jeong Koo Kim
Il Keun Kwon
Leon M. Bellan
Hak-Joon Sung
author_facet Jung Bok Lee
Daniel A. Balikov
Jae Won Yang
Ki Seok Kim
Hun Kuk Park
Jeong Koo Kim
Il Keun Kwon
Leon M. Bellan
Hak-Joon Sung
author_sort Jung Bok Lee
collection DOAJ
description Polymers have been used extensively taking forms as scaffolds, patterned surface and nanoparticle for regenerative medicine applications. Angiogenesis is an essential process for successful tissue regeneration, and endothelial cell–cell interaction plays a pivotal role in regulating their tight junction formation, a hallmark of angiogenesis. Though continuous progress has been made, strategies to promote angiogenesis still rely on small molecule delivery or nuanced scaffold fabrication. As such, the recent paradigm shift from top-down to bottom-up approaches in tissue engineering necessitates development of polymer-based modular engineering tools to control angiogenesis. Here, we developed cationic nanocylinders (NCs) as inducers of cell–cell interaction and investigated their effect on angiogenic activities of human umbilical vein endothelial cells (HUVECs) in vitro. Electrospun poly (l-lactic acid) (PLLA) fibers were aminolyzed to generate positively charged NCs. The aninolyzation time was changed to produce two different aspect ratios of NCs. When HUVECs were treated with NCs, the electrostatic interaction of cationic NCs with negatively charged plasma membranes promoted migration, permeability and tubulogenesis of HUVECs compared to no treatment. This effect was more profound when the higher aspect ratio NC was used. The results indicate these NCs can be used as a new tool for the bottom-up approach to promote angiogenesis.
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spelling doaj.art-b13d9ba10c9c41a6bf1bcc393b41ecc92022-12-22T03:47:41ZengMDPI AGPolymers2073-43602016-01-01811510.3390/polym8010015polym8010015Cationic Nanocylinders Promote Angiogenic Activities of Endothelial CellsJung Bok Lee0Daniel A. Balikov1Jae Won Yang2Ki Seok Kim3Hun Kuk Park4Jeong Koo Kim5Il Keun Kwon6Leon M. Bellan7Hak-Joon Sung8Department of Biomedical Engineering, Vanderbilt University, Nashville, TN 37212, USADepartment of Biomedical Engineering, Vanderbilt University, Nashville, TN 37212, USADepartment of Internal Medicine, Yonsei University of Wonju College of Medicine, Wonju, Gangwon 220-701, KoreaDepartment of Medical Engineering, College of Medicine, Kyung Hee University, Seoul 130-701, KoreaDepartment of Medical Engineering, College of Medicine, Kyung Hee University, Seoul 130-701, KoreaDepartment of Biomedical Engineering, Vanderbilt University, Nashville, TN 37212, USADepartment of Maxillofacial Biomedical Engineering and Institute of Oral Biology, School of Dentistry, Kyung Hee University, Seoul 130-701, KoreaDepartment of Biomedical Engineering, Vanderbilt University, Nashville, TN 37212, USADepartment of Biomedical Engineering, Vanderbilt University, Nashville, TN 37212, USAPolymers have been used extensively taking forms as scaffolds, patterned surface and nanoparticle for regenerative medicine applications. Angiogenesis is an essential process for successful tissue regeneration, and endothelial cell–cell interaction plays a pivotal role in regulating their tight junction formation, a hallmark of angiogenesis. Though continuous progress has been made, strategies to promote angiogenesis still rely on small molecule delivery or nuanced scaffold fabrication. As such, the recent paradigm shift from top-down to bottom-up approaches in tissue engineering necessitates development of polymer-based modular engineering tools to control angiogenesis. Here, we developed cationic nanocylinders (NCs) as inducers of cell–cell interaction and investigated their effect on angiogenic activities of human umbilical vein endothelial cells (HUVECs) in vitro. Electrospun poly (l-lactic acid) (PLLA) fibers were aminolyzed to generate positively charged NCs. The aninolyzation time was changed to produce two different aspect ratios of NCs. When HUVECs were treated with NCs, the electrostatic interaction of cationic NCs with negatively charged plasma membranes promoted migration, permeability and tubulogenesis of HUVECs compared to no treatment. This effect was more profound when the higher aspect ratio NC was used. The results indicate these NCs can be used as a new tool for the bottom-up approach to promote angiogenesis.http://www.mdpi.com/2073-4360/8/1/15cationic nanocylindercell–cell interactionendothelial cellsmigrationtubulogenesis
spellingShingle Jung Bok Lee
Daniel A. Balikov
Jae Won Yang
Ki Seok Kim
Hun Kuk Park
Jeong Koo Kim
Il Keun Kwon
Leon M. Bellan
Hak-Joon Sung
Cationic Nanocylinders Promote Angiogenic Activities of Endothelial Cells
Polymers
cationic nanocylinder
cell–cell interaction
endothelial cells
migration
tubulogenesis
title Cationic Nanocylinders Promote Angiogenic Activities of Endothelial Cells
title_full Cationic Nanocylinders Promote Angiogenic Activities of Endothelial Cells
title_fullStr Cationic Nanocylinders Promote Angiogenic Activities of Endothelial Cells
title_full_unstemmed Cationic Nanocylinders Promote Angiogenic Activities of Endothelial Cells
title_short Cationic Nanocylinders Promote Angiogenic Activities of Endothelial Cells
title_sort cationic nanocylinders promote angiogenic activities of endothelial cells
topic cationic nanocylinder
cell–cell interaction
endothelial cells
migration
tubulogenesis
url http://www.mdpi.com/2073-4360/8/1/15
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