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Microfluidic assay of endothelial cell migration in 3D interpenetrating polymer semi-network HA-Collagen hydrogel

Authors
Jeong, Gi SeokKwon, Gu HanKang, Ah RanJung, Bo YoungPark, YongdooChung, SeokLee, Sang-Hoon
Issue Date
8월-2011
Publisher
SPRINGER
Keywords
Cell migration; 3D matrix; Collagen; Hyaluronic acid; Semi-interpenetrating networks; MMP
Citation
BIOMEDICAL MICRODEVICES, v.13, no.4, pp.717 - 723
Indexed
SCIE
SCOPUS
Journal Title
BIOMEDICAL MICRODEVICES
Volume
13
Number
4
Start Page
717
End Page
723
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/111839
DOI
10.1007/s10544-011-9541-7
ISSN
1387-2176
Abstract
Cell migration through the extracellular matrix (ECM) is one of the key features for physiological and pathological processes such as angiogenesis, cancer metastasis, and wound healing. In particular, the quantitative assay of endothelial cell migration under the well-defined three dimensional (3D) microenvironment is important to analyze the angiogenesis mechanism. In this study, we report a microfluidic assay of endothelial cell sprouting and migration into an interpenetrating polymer semi-network HA-Collagen (SIPNs CH) hydrogel as ECM providing an enhanced in vivo mimicking 3D microenvironment to cells. The microfluidic chip could provide a well-controlled gradient of growth factor to cells, whereas the hydrogel could mimic a well-defined 3D microenvironment in vivo. (In addition/Furthermore, the microfluidic chip gives a well-controlled gradient of growth factor to cells) For this reason, three types of hydrogel, composed of semi-interpenetrating networks of collagen and hyaluronic acid were prepared, and firstly we proved the role of the hydrogel in endothelial cell migration. The diffusion property and swelling ratio of the hydrogel were characterized. It modulated the migration of endothelial cells in quantified manner, also being influenced by additional synthesis of Matrix metalloproteinase(MMP)-sensitive remodeling peptides and Arginine-glycine-lycinee (RGD) cell adhesion peptides. We successfully established a novel cell migration platform by changing major determinants such as ECM material under biochemical synthesis and under growth factor gradients in a microfluidic manner.
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Graduate School > Department of Biomedical Sciences > 1. Journal Articles
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