Abstract
Development and study of cell-cultured constructs, such as tissue-engineering scaffolds or organ-on-a-chip platforms require a comprehensive, representative view on the cells inside the used materials. However, common characteristics of biomedical materials, for example, in porous, fibrous, rough-surfaced, and composite materials, can severely disturb low-energy imaging. In order to image and quantify cell structures in optically challenging samples, we combined labeling, 3D X-ray imaging, and in silico processing into a methodological pipeline. Cell-structure images were acquired by a tube-source X-ray microtomography device and compared to optical references for assessing the visual and quantitative accuracy. The spatial coverage of the X-ray imaging was demonstrated by investigating stem-cell nuclei inside clinically relevant-sized tissue-engineering scaffolds (5x13 mm) that were difficult to examine with the optical methods. Our results highlight the potential of the readily available X-ray microtomography devices that can be used to thoroughly study relative large cell-cultured samples with microscopic 3D accuracy.
Original language | English |
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Article number | 548 |
Journal | Communications biology |
Volume | 3 |
Issue number | 1 |
DOIs | |
Publication status | Published - 2020 |
Publication type | A1 Journal article-refereed |
Publication forum classification
- Publication forum level 1
ASJC Scopus subject areas
- General Biochemistry,Genetics and Molecular Biology
- General Agricultural and Biological Sciences
- Medicine (miscellaneous)
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ThreeDROQA function
Hannula, M. (Creator) & Tamminen, I. (Creator), Zenodo, 30 Aug 2020
DOI: 10.5281/zenodo.4008538, https://github.com/hannulam/ThreeDROQA_function/tree/v1.0.1
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Tampere Imaging Facility (TIF) - light microscopy core services
Ihalainen, T. (Manager), Erämies, S. (Contact) & Paloheimo, O. (Contact)
Facility/equipment: Facility
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