A massively multi-scale approach to characterizing tissue architecture by synchrotron micro-CT applied to the human placenta

Author:

Tun W. M.1ORCID,Poologasundarampillai G.2ORCID,Bischof H.34,Nye G.5,King O. N. F.1ORCID,Basham M.16ORCID,Tokudome Y.7,Lewis R. M.8ORCID,Johnstone E. D.34,Brownbill P.34ORCID,Darrow M.9ORCID,Chernyavsky I. L.3410ORCID

Affiliation:

1. Diamond Light Source, Didcot OX11 0DE, UK

2. School of Dentistry, University of Birmingham, Birmingham B15 2TT, UK

3. Maternal and Fetal Health Research Centre, School of Medical Sciences, University of Manchester, Manchester, UK

4. MAHSC, St Mary's Hospital, NHS MFT, Manchester M13 9WL, UK

5. Chester Medical School, University of Chester, Chester CH1 4BJ, UK

6. Rosalind Franklin Institute, Didcot OX11 0DE, UK

7. Department of Materials Science, Graduate School of Engineering, Osaka Prefecture University, Osaka 599-8531, Japan

8. Faculty of Medicine, University of Southampton, Southampton SO16 6YD, UK

9. SPT Labtech Ltd, Melbourn SG8 6HB, UK

10. Department of Mathematics, University of Manchester, Manchester M13 9PL, UK

Abstract

Multi-scale structural assessment of biological soft tissue is challenging but essential to gain insight into structure–function relationships of tissue/organ. Using the human placenta as an example, this study brings together sophisticated sample preparation protocols, advanced imaging and robust, validated machine-learning segmentation techniques to provide the first massively multi-scale and multi-domain information that enables detailed morphological and functional analyses of both maternal and fetal placental domains. Finally, we quantify the scale-dependent error in morphological metrics of heterogeneous placental tissue, estimating the minimal tissue scale needed in extracting meaningful biological data. The developed protocol is beneficial for high-throughput investigation of structure–function relationships in both normal and diseased placentas, allowing us to optimize therapeutic approaches for pathological pregnancies. In addition, the methodology presented is applicable in the characterization of tissue architecture and physiological behaviours of other complex organs with similarity to the placenta, where an exchange barrier possesses circulating vascular and avascular fluid spaces.

Funder

Engineering and Physical Sciences Research Council

Medical Research Council

Wellcome Trust

Great Britain Sasakawa Foundation

Publisher

The Royal Society

Subject

Biomedical Engineering,Biochemistry,Biomaterials,Bioengineering,Biophysics,Biotechnology

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