Quantitative intrinsic auto-cathodoluminescence can resolve spectral signatures of tissue-isolated collagen extracellular matrix

Zielinski, Marcin S. and Vardar, Elif and Vythilingam, Ganesh and Engelhardt, Eva-Maria and Hubbell, Jeffrey A. and Frey, Peter and Larsson, Hans M. (2019) Quantitative intrinsic auto-cathodoluminescence can resolve spectral signatures of tissue-isolated collagen extracellular matrix. Communications Biology, 2 (1). p. 69. ISSN 2399-3642, DOI https://doi.org/10.1038/s42003-019-0313-x.

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Official URL: https://doi.org/10.1038/s42003-019-0313-x

Abstract

By analyzing isolated collagen gel samples, we demonstrated in situ detection of spectrally deconvoluted auto-cathodoluminescence signatures of specific molecular content with precise spatial localization over a maximum field of view of 300 µm. Correlation of the secondary electron and the hyperspectral images proved ~40 nm resolution in the optical channel, obtained due to a short carrier diffusion length, suppressed by fibril dimensions and poor electrical conductivity specific to their organic composition. By correlating spectrally analyzed auto-cathodoluminescence with mass spectroscopy data, we differentiated spectral signatures of two extracellular matrices, namely human fibrin complex and rat tail collagen isolate, and uncovered differences in protein distributions of isolated extracellular matrix networks of heterogeneous populations. Furthermore, we demonstrated that cathodoluminescence can monitor the progress of a human cell-mediated remodeling process, where human collagenous matrix was deposited within a rat collagenous matrix. The revealed change of the heterogeneous biological composition was confirmed by mass spectroscopy.

Item Type: Article
Funders: UNSPECIFIED
Uncontrolled Keywords: Cathodoluminescence; Electron beams; Optical microscopes
Subjects: R Medicine
Divisions: Faculty of Medicine
Depositing User: Ms. Juhaida Abd Rahim
Date Deposited: 31 Oct 2019 08:31
Last Modified: 31 Oct 2019 08:31
URI: http://eprints.um.edu.my/id/eprint/22894

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