Home > Research > Publications & Outputs > Detection of early stage changes associated wit...

Associated organisational unit

Electronic data

  • cytometry accepted manuscript (1)

    Rights statement: © 2015 The Authors. Published by Wiley Periodicals, Inc. on behalf of the International Society for Advancement of Cytometry. This is an open access article under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and the content is offered under identical terms.

    Accepted author manuscript, 886 KB, PDF document

    Available under license: CC BY-NC: Creative Commons Attribution-NonCommercial 4.0 International License

Links

Text available via DOI:

View graph of relations

Detection of early stage changes associated with adipogenesis using Raman spectroscopy under aseptic conditions

Research output: Contribution to journalJournal articlepeer-review

Published
  • Adam Mitchell
  • Lorna Ashton
  • Xuebin B Yang
  • Royston Goodacre
  • Alistair Smith
  • Jennifer Kirkham
Close
<mark>Journal publication date</mark>2015
<mark>Journal</mark>Cytometry Part A
Issue number11
Volume87
Number of pages8
Pages (from-to)1012-1019
Publication StatusPublished
Early online date6/10/15
<mark>Original language</mark>English

Abstract

There is growing interest in the development of methods capable of non-invasive characterisation of stem cells prior to their use in cell based therapies. Raman spectroscopy has previously been used to detect biochemical changes commensurate with the osteogenic, cardiogenic and neurogenic differentiation of stem cells. The aim of this study was to characterise the adipogenic differentiation of live adipose derived stem cells (ASCs) under aseptic conditions. ASCs where cultured in adipogenic or basal culture medium for 14 days in customised culture flasks containing quartz windows. Raman spectra were acquired every 3 days. Principal component analysis (PCA) was used to identify spectral changes in the cultures over time. Adipogenic differentiation was confirmed using qRT-PCR for the marker genes PPARγ and ADIPOQ and Oil red O staining performed. PCA demonstrated that lipid associated spectral features varied throughout ASC differentiation with the earliest detection of the lipid associated peak at 1438 cm-1 after 3 days of induction. After 7 days of culture there were clear differences between the spectra acquired from ASCs in adipogenic or basal culture medium. No changes were observed in the spectra acquired from undifferentiated ASCs. Significant up-regulation in the expression of both PPARγ and ADIPOQ genes (p<0.001) was observed after 14 days of differentiation as was prominent Oil red O staining. However, the Raman sampling process resulted in weaker gene expression compared with ASCs that had not undergone Raman analysis. This study demonstrated that Raman spectroscopy can be used to detect biochemical changes associated with adipogenic differentiation in a non-invasive and aseptic manner and that this can be achieved as early as three days into the differentiation process.

Bibliographic note

© 2015 The Authors. Published by Wiley Periodicals, Inc. on behalf of the International Society for Advancement of Cytometry. This is an open access article under the terms of the Creative Commons Attribution License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and the content is offered under identical terms.