Loughborough University
Leicestershire, UK
LE11 3TU
+44 (0)1509 263171
Loughborough University

Loughborough University Institutional Repository

Please use this identifier to cite or link to this item: https://dspace.lboro.ac.uk/2134/13498

Title: Incorporation of hydroxyapatite sol into collagen gel to regulate the contraction mediated by human bone marrow-derived stromal cells
Authors: Liu, Yang
Williams, David J.
Keywords: Biomechanics
Cell mechanics
Biological cells
Issue Date: 2010
Publisher: © IEEE
Citation: LIU, Y. and WILLIAMS, D.J., 2010. Incorporation of hydroxyapatite sol into collagen gel to regulate the contraction mediated by human bone marrow-derived stromal cells. IEEE Transactions on Nanobioscience, 9 (1), pp.1-11.
Abstract: In this paper, hydroxyapatite (HA) sol composed of nanosized HA particles was incorporated into collagen gel to regulate cell-mediated collagen contraction. Human bone marrow derived stromal cells (hMSCs) were cultured for 37 days in gels with HA to collagen ratios of 0:1, 0.5:1, 1:1, 1.5:1, and 2:1, respectively. The contraction of gels was evaluated by measuring diameter change with incubation time, and the microstructure of gels at the end of culture was visualized by SEM. The cytotoxicity of HA sol was evaluated according to the percentage of maximum lactate dehydrogenase (LDH) release from hMSCs. A combination of Hoechst 33342, propidium iodide, and calcein esters was used for imaging the live/dead cells and the distribution of loaded cells within the constructs. By incorporating HA sol into the collagen gel, the hMSCs medicated contraction was delayed and the extent of contraction was reduced as the proportion of HA relative to the collagen increased. Depending on the ratio of HA sol incorporated within the collagen gel, hMSC cells revealed different morphology and a change in the distribution of loaded cells within the gels. No significant cytotoxicity was noticed as a consequence of incorporating HA sol into the collagen lattice.
Description: This article is closed access.
Sponsor: This work was supported by the U.K. Engineering and Physical Sciences Research Council funded Innovative Manufacturing Grand Challenge in Regenerative Medicine, remedi, a partnership of Loughborough, Nottingham, Cambridge, Birmingham, Ulster and Liverpool universities, and industry and agency stakeholders. The work of Y. Liu was supported by a Research Councils United Kingdom fellowship.
Version: Published
DOI: 10.1109/TNB.2009.2034654
URI: https://dspace.lboro.ac.uk/2134/13498
Publisher Link: http://dx.doi.org/10.1109/TNB.2009.2034654
ISSN: 1536-1241
Appears in Collections:Closed Access (Mechanical, Electrical and Manufacturing Engineering)

Files associated with this item:

File Description SizeFormat
IEEE collagen and nano HA.pdfPublished version832.41 kBAdobe PDFView/Open


SFX Query

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