In situ thermal gelling polypeptide for chondrocytes 3D culture

Authors
Choi, Bo GyuPark, Min HeeCho, So-HyeJoo, Min KyungOh, Hye JinKim, Eun HyePark, KwideokHan, Dong KeunJeong, Byeongmoon
Issue Date
2010-12
Publisher
ELSEVIER SCI LTD
Citation
BIOMATERIALS, v.31, no.35, pp.9266 - 9272
Abstract
In the search for a cell-instructive or cell-interactive artificial extracellular matrix, synthetic hydrogels have been extensively investigated to apply three-dimensional (3D) cell culture and tissue engineering. Here, we are reporting a reverse thermal gelling L/DL-polyalanine block copolymer aqueous solution for chondrocyte 3D culture. The polymer aqueous solution undergoes sol-to-gel transition as the temperature increases, thus forming a 3D cell encapsulating scaffold in situ at 37 degrees C. In particular, the fraction of the beta-sheet structure of the polyalanine dictated the population and thickness of fibrous nanostructure of the hydrogel, which in turn affected the proliferation and protein expression of the encapsulated chondrocytes. As an injectable tissue engineering system of chondrocytes, very promising results were confirmed for nude mice, using the current polypeptide aqueous solution. This paper not only provides important clues in designing an artificial extracellular matrix but also proves the significance of thermal gelling polypeptide as a minimally-invasive tissue engineering scaffold. (C) 2010 Elsevier Ltd. All rights reserved.
Keywords
DRUG-DELIVERY; CELL-CULTURE; STEM-CELLS; HYDROGELS; DIFFERENTIATION; SCAFFOLDS; BIOMATERIALS; DRUG-DELIVERY; CELL-CULTURE; STEM-CELLS; HYDROGELS; DIFFERENTIATION; SCAFFOLDS; BIOMATERIALS; Secondary structure; Peptide; Thermally responsive material; Hydrogel; Chondrocyte; Cell culture
ISSN
0142-9612
URI
https://pubs.kist.re.kr/handle/201004/130871
DOI
10.1016/j.biomaterials.2010.08.067
Appears in Collections:
KIST Article > 2010
Files in This Item:
There are no files associated with this item.
Export
RIS (EndNote)
XLS (Excel)
XML

qrcode

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.

BROWSE