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Tomography studies of human foreskin fibroblasts on polymer yarns

Tomography studies of human foreskin fibroblasts on polymer yarns
Tomography studies of human foreskin fibroblasts on polymer yarns
Cell culture experiments are usually performed as in vitro studies based on 2D seeding and characterization (light microscopy). With respect to the in vivo situation, however, 2D studies are often inappropriate due to the 3D character of living tissue in nature. Textiles with their versatile 3D structures are chosen as suitable scaffolds in tissue engineering for 3D in vitro studies. Micro-computed tomography using X-rays (?CT) belongs to the most promising techniques for isotropic, noninvasive 3D characterization. Using synchrotron radiation (SR?CT) the spatial resolution can be extended to the sub-micrometer range well below cell size. ?CT does not need vacuum conditions making experiments in the hydrated state possible, as we show by data from SR?CT acquired at second and third-generation synchrotron sources. We seeded human foreskin fibroblasts on polymer multifilament yarns. These composites, embedded in a hydrogel or fluid, are held in thin-walled glass capillaries. Since the composites consist of light elements, the cells have to be labeled for visualization by the use of highly absorptive agents, osmium and gold. In order to hold the label concentration as low as possible, we present a way to choose the photon energy for which the minimum concentration is reached. Differences in threshold selection for second- and third-generation synchrotron sources are pointed out, revealing the advantages of both types with respect to quantitative analysis. The study is based on appropriate staining methods and protocols developed in our laboratory. With the results we demonstrate that SR?CT yields images similar to established electron and light microscopy but uncovers also the microstructure in 3D space.
computerized tomography, synchrotron radiation, cell complexes (geometry and topology), image processing algorithms, biological physics spectroscopic- and microscopic techniques
0168-583X
397-405
Thurner, Philipp J.
ab711ddd-784e-48de-aaad-f56aec40f84f
Müller, Bert
acba4294-b684-4a09-81ac-32de31d39923
Beckmann, Felix
9c0d47e5-e36b-4523-b6b6-0d65a708441b
Weitkamp, Timm
b9a2c880-940e-4149-8c1a-0c52e7dbd561
Rau, Christoph
f29342b8-92a1-4855-a20c-3960de6e6053
Müller, Ralph
f881853a-540f-48f1-bb6d-e0cf1894e036
Hubbell, Jeffrey A.
c9b5c639-f582-43a8-b82f-0d5da8a0d9f8
Sennhauser, Urs
3c0e14aa-da0a-48da-bb7b-c65401b1d01b
Thurner, Philipp J.
ab711ddd-784e-48de-aaad-f56aec40f84f
Müller, Bert
acba4294-b684-4a09-81ac-32de31d39923
Beckmann, Felix
9c0d47e5-e36b-4523-b6b6-0d65a708441b
Weitkamp, Timm
b9a2c880-940e-4149-8c1a-0c52e7dbd561
Rau, Christoph
f29342b8-92a1-4855-a20c-3960de6e6053
Müller, Ralph
f881853a-540f-48f1-bb6d-e0cf1894e036
Hubbell, Jeffrey A.
c9b5c639-f582-43a8-b82f-0d5da8a0d9f8
Sennhauser, Urs
3c0e14aa-da0a-48da-bb7b-c65401b1d01b

Thurner, Philipp J., Müller, Bert, Beckmann, Felix, Weitkamp, Timm, Rau, Christoph, Müller, Ralph, Hubbell, Jeffrey A. and Sennhauser, Urs (2003) Tomography studies of human foreskin fibroblasts on polymer yarns. Nuclear Instruments and Methods in Physics Research Section B: Beam Interactions with Materials and Atoms, 200, 397-405. (doi:10.1016/S0168-583X(02)01729-9).

Record type: Article

Abstract

Cell culture experiments are usually performed as in vitro studies based on 2D seeding and characterization (light microscopy). With respect to the in vivo situation, however, 2D studies are often inappropriate due to the 3D character of living tissue in nature. Textiles with their versatile 3D structures are chosen as suitable scaffolds in tissue engineering for 3D in vitro studies. Micro-computed tomography using X-rays (?CT) belongs to the most promising techniques for isotropic, noninvasive 3D characterization. Using synchrotron radiation (SR?CT) the spatial resolution can be extended to the sub-micrometer range well below cell size. ?CT does not need vacuum conditions making experiments in the hydrated state possible, as we show by data from SR?CT acquired at second and third-generation synchrotron sources. We seeded human foreskin fibroblasts on polymer multifilament yarns. These composites, embedded in a hydrogel or fluid, are held in thin-walled glass capillaries. Since the composites consist of light elements, the cells have to be labeled for visualization by the use of highly absorptive agents, osmium and gold. In order to hold the label concentration as low as possible, we present a way to choose the photon energy for which the minimum concentration is reached. Differences in threshold selection for second- and third-generation synchrotron sources are pointed out, revealing the advantages of both types with respect to quantitative analysis. The study is based on appropriate staining methods and protocols developed in our laboratory. With the results we demonstrate that SR?CT yields images similar to established electron and light microscopy but uncovers also the microstructure in 3D space.

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More information

Published date: January 2003
Keywords: computerized tomography, synchrotron radiation, cell complexes (geometry and topology), image processing algorithms, biological physics spectroscopic- and microscopic techniques

Identifiers

Local EPrints ID: 48952
URI: http://eprints.soton.ac.uk/id/eprint/48952
ISSN: 0168-583X
PURE UUID: cc87ffc2-fdc1-48dd-b2f0-dfac1fabe198
ORCID for Philipp J. Thurner: ORCID iD orcid.org/0000-0001-7588-9041

Catalogue record

Date deposited: 18 Oct 2007
Last modified: 15 Mar 2024 09:51

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Contributors

Author: Bert Müller
Author: Felix Beckmann
Author: Timm Weitkamp
Author: Christoph Rau
Author: Ralph Müller
Author: Jeffrey A. Hubbell
Author: Urs Sennhauser

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