Quantitative non-invasive cell characterisation and discrimination based on multispectral autofluorescence features

Sci Rep. 2016 Mar 31:6:23453. doi: 10.1038/srep23453.

Abstract

Automated and unbiased methods of non-invasive cell monitoring able to deal with complex biological heterogeneity are fundamentally important for biology and medicine. Label-free cell imaging provides information about endogenous autofluorescent metabolites, enzymes and cofactors in cells. However extracting high content information from autofluorescence imaging has been hitherto impossible. Here, we quantitatively characterise cell populations in different tissue types, live or fixed, by using novel image processing and a simple multispectral upgrade of a wide-field fluorescence microscope. Our optimal discrimination approach enables statistical hypothesis testing and intuitive visualisations where previously undetectable differences become clearly apparent. Label-free classifications are validated by the analysis of Classification Determinant (CD) antigen expression. The versatility of our method is illustrated by detecting genetic mutations in cancer, non-invasive monitoring of CD90 expression, label-free tracking of stem cell differentiation, identifying stem cell subpopulations with varying functional characteristics, tissue diagnostics in diabetes, and assessing the condition of preimplantation embryos.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Blastocyst / metabolism
  • Blastocyst / ultrastructure
  • Cell Differentiation
  • Cell Line, Tumor
  • Cell Tracking / instrumentation
  • Cell Tracking / methods*
  • Diabetes Mellitus, Experimental / genetics
  • Diabetes Mellitus, Experimental / metabolism*
  • Diabetes Mellitus, Experimental / pathology
  • Gene Expression
  • Gene Expression Regulation
  • Humans
  • Image Processing, Computer-Assisted / statistics & numerical data
  • Membrane Proteins / genetics
  • Membrane Proteins / metabolism
  • Mice
  • Mutation*
  • Optical Imaging / methods*
  • Optical Imaging / statistics & numerical data
  • Pancreatic Neoplasms / genetics
  • Pancreatic Neoplasms / metabolism
  • Pancreatic Neoplasms / ultrastructure*
  • Receptors, Progesterone / genetics
  • Receptors, Progesterone / metabolism
  • Stem Cells / cytology
  • Stem Cells / metabolism
  • Thy-1 Antigens / genetics*
  • Thy-1 Antigens / metabolism

Substances

  • Membrane Proteins
  • PGRMC1 protein, mouse
  • Receptors, Progesterone
  • Thy-1 Antigens