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3D morphology of cell cultures: a quantitative approach using micrometer synchrotron light tomography

3D morphology of cell cultures: a quantitative approach using micrometer synchrotron light tomography
3D morphology of cell cultures: a quantitative approach using micrometer synchrotron light tomography
Current issues in both tissue engineering and cell biology deal with cell behavior extensively in 3D. Here, we explore synchrotron radiation micro-computed tomography as a tool for morphological characterization of such 3D cellular constructs, providing micrometer resolution in soft and hard tissues. Novel image processing techniques allowed quantification of local and global cell distributions, cell density, adhesive cell culture surface, and scaffold geometry. For proof of concept, we applied this technique to characterize the morphology of two cell cultures of different phenotypes, namely human dermal fibroblasts and mouse calvarial osteoblast-like cells, both seeded on a polymer multifilament yarn. From 3D visualizations in these case studies, we saw that the fibroblasts spanned between the yarn filaments and in this way encapsulated the yarn, whereas the osteoblast-like cells lined the filament surfaces and did not span between them. Differences found in cell distribution as a function of distance to the median yarn axis and the closest filament surface, respectively, quantified these qualitative impressions gained from 3D visualizations. Moreover, the volume-normalized adhesive surface differed by one order of magnitude between the two phenotypes. Our approach allows quantitative correlation of local scaffold geometry and cell morphology. It can be used to investigate the influence of cell phenotype as well as various biochemical agents on tissue engineering constructs and the behavior of cells in culture.
cell culture morphology, 3D cell cultures, cell imaging, image processing, tomography, synchrotron radiation
1059-910X
289-298
Thurner, Philipp J.
ab711ddd-784e-48de-aaad-f56aec40f84f
Müller, Ralph
f881853a-540f-48f1-bb6d-e0cf1894e036
Raeber, George
61774412-ff70-4b58-a006-642fce11417e
Sennhauser, Urs
3c0e14aa-da0a-48da-bb7b-c65401b1d01b
Hubbell, Jeffrey A.
c9b5c639-f582-43a8-b82f-0d5da8a0d9f8
Thurner, Philipp J.
ab711ddd-784e-48de-aaad-f56aec40f84f
Müller, Ralph
f881853a-540f-48f1-bb6d-e0cf1894e036
Raeber, George
61774412-ff70-4b58-a006-642fce11417e
Sennhauser, Urs
3c0e14aa-da0a-48da-bb7b-c65401b1d01b
Hubbell, Jeffrey A.
c9b5c639-f582-43a8-b82f-0d5da8a0d9f8

Thurner, Philipp J., Müller, Ralph, Raeber, George, Sennhauser, Urs and Hubbell, Jeffrey A. (2005) 3D morphology of cell cultures: a quantitative approach using micrometer synchrotron light tomography. Microscopy Research and Technique, 66 (6), 289-298. (doi:10.1002/jemt.20170).

Record type: Article

Abstract

Current issues in both tissue engineering and cell biology deal with cell behavior extensively in 3D. Here, we explore synchrotron radiation micro-computed tomography as a tool for morphological characterization of such 3D cellular constructs, providing micrometer resolution in soft and hard tissues. Novel image processing techniques allowed quantification of local and global cell distributions, cell density, adhesive cell culture surface, and scaffold geometry. For proof of concept, we applied this technique to characterize the morphology of two cell cultures of different phenotypes, namely human dermal fibroblasts and mouse calvarial osteoblast-like cells, both seeded on a polymer multifilament yarn. From 3D visualizations in these case studies, we saw that the fibroblasts spanned between the yarn filaments and in this way encapsulated the yarn, whereas the osteoblast-like cells lined the filament surfaces and did not span between them. Differences found in cell distribution as a function of distance to the median yarn axis and the closest filament surface, respectively, quantified these qualitative impressions gained from 3D visualizations. Moreover, the volume-normalized adhesive surface differed by one order of magnitude between the two phenotypes. Our approach allows quantitative correlation of local scaffold geometry and cell morphology. It can be used to investigate the influence of cell phenotype as well as various biochemical agents on tissue engineering constructs and the behavior of cells in culture.

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More information

Published date: 7 July 2005
Keywords: cell culture morphology, 3D cell cultures, cell imaging, image processing, tomography, synchrotron radiation

Identifiers

Local EPrints ID: 48843
URI: http://eprints.soton.ac.uk/id/eprint/48843
ISSN: 1059-910X
PURE UUID: b85a001a-91cb-49a9-8097-c7211f83138c
ORCID for Philipp J. Thurner: ORCID iD orcid.org/0000-0001-7588-9041

Catalogue record

Date deposited: 16 Oct 2007
Last modified: 15 Mar 2024 09:50

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Contributors

Author: Ralph Müller
Author: George Raeber
Author: Urs Sennhauser
Author: Jeffrey A. Hubbell

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