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Multiparameter mechanical and morphometric screening of cells.
Masaeli, Mahdokht; Gupta, Dewal; O'Byrne, Sean; Tse, Henry T K; Gossett, Daniel R; Tseng, Peter; Utada, Andrew S; Jung, Hea-Jin; Young, Stephen; Clark, Amander T; Di Carlo, Dino.
Afiliação
  • Masaeli M; Department of Bioengineering, University of California, Los Angeles, CA, USA.
  • Gupta D; California NanoSystems Institute, Los Angeles, CA, USA.
  • O'Byrne S; Division of Cardiovascular Medicine, Stanford University School of Medicine, Stanford, CA, USA.
  • Tse HT; Department of Bioengineering, University of California, Los Angeles, CA, USA.
  • Gossett DR; Department of Bioengineering, University of California, Los Angeles, CA, USA.
  • Tseng P; California NanoSystems Institute, Los Angeles, CA, USA.
  • Utada AS; Department of Bioengineering, University of California, Los Angeles, CA, USA.
  • Jung HJ; California NanoSystems Institute, Los Angeles, CA, USA.
  • Young S; CytoVale Inc, South San Francisco, CA, USA.
  • Clark AT; Department of Bioengineering, University of California, Los Angeles, CA, USA.
  • Di Carlo D; California NanoSystems Institute, Los Angeles, CA, USA.
Sci Rep ; 6: 37863, 2016 12 02.
Article em En | MEDLINE | ID: mdl-27910869
ABSTRACT
We introduce a label-free method to rapidly phenotype and classify cells purely based on physical properties. We extract 15 biophysical parameters from cells as they deform in a microfluidic stretching flow field via high-speed microscopy and apply machine-learning approaches to discriminate different cell types and states. When employing the full 15 dimensional dataset, the technique robustly classifies individual cells based on their pluripotency, with accuracy above 95%. Rheological and morphological properties of cells while deforming were critical for this classification. We also show the application of this method in accurate classifying cells based on their viability, drug screening and detecting populations of malignant cells in mixed samples. We show that some of the extracted parameters are not linearly independent, and in fact we reach maximum classification accuracy by using only a subset of parameters. However, the informative subsets could vary depending on cell types in the sample. This work shows the utility of an assay purely based on intrinsic biophysical properties of cells to identify changes in cell state. In addition to a label-free alternative to flow cytometry in certain applications, this work, also can provide novel intracellular metrics that would not be feasible with labeled approaches (i.e. flow cytometry).
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Células-Tronco Embrionárias / Citometria de Fluxo / Aprendizado de Máquina Tipo de estudo: Diagnostic_studies / Screening_studies Limite: Animals / Humans Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Células-Tronco Embrionárias / Citometria de Fluxo / Aprendizado de Máquina Tipo de estudo: Diagnostic_studies / Screening_studies Limite: Animals / Humans Idioma: En Ano de publicação: 2016 Tipo de documento: Article