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Deciphering the internal complexity of living cells with quantitative phase microscopy: a multiscale approach

dc.contributor.authorMARTINEZ-TORRES, Cristina
dc.contributor.authorLAPERROUSAZ, Bastien
dc.contributor.authorBERGUIGA, Lotfi
dc.contributor.authorBOYER-PROVERA, Elise
dc.contributor.authorELEZGARAY, Juan
dc.contributor.authorNICOLINI, Franck E.
dc.contributor.authorMAGUER-SATTA, Veronique
dc.contributor.authorARNEODO, Alain
dc.contributor.authorARGOUL, Francoise
dc.date.accessioned2020-09-03T08:02:01Z
dc.date.available2020-09-03T08:02:01Z
dc.date.issued2015
dc.identifier.issn1083-3668
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/10953
dc.description.abstractEnThe distribution of refractive indices (RIs) of a living cell contributes in a nonintuitive manner to its optical phase image and quite rarely can be inverted to recover its internal structure. The interpretation of the quantitative phase images of living cells remains a difficult task because (1) we still have very little knowledge on the impact of its internal macromolecular complexes on the local RI and (2) phase changes produced by light propagation through the sample are mixed with diffraction effects by the internal cell bodies. We propose to implement a two-dimensional wavelet-based contour chain detection method to distinguish internal boundaries based on their greatest optical path difference gradients. These contour chains correspond to the highest image phase contrast and follow the local RI inhomogeneities linked to the intracellular structural intricacy. Their statistics and spatial distribution are the morphological indicators suited for comparing cells of different origins and/ or to follow their transformation in pathologic situations. We use this method to compare nonadherent blood cells from primary and laboratory culture origins and to assess the internal transformation of hematopoietic stem cells by the transduction of the BCR-ABL oncogene responsible for the chronic myelogenous leukemia. (C) 2015 Society of Photo-Optical Instrumentation Engineers (SPIE)
dc.language.isoen
dc.title.enDeciphering the internal complexity of living cells with quantitative phase microscopy: a multiscale approach
dc.typeArticle de revue
dc.identifier.doi10.1117/1.jbo.20.9.096005
dc.subject.halChimie/Matériaux
bordeaux.journalJournal of Biomedical Optics
bordeaux.volume20
bordeaux.hal.laboratoriesInstitut de Chimie & de Biologie des Membranes & des Nano-objets (CBMN) - UMR 5248*
bordeaux.hal.laboratoriesInstitut de Chimie & de Biologie des Membranes & des Nano-objets (CBMN, UMR 5248)
bordeaux.issue9
bordeaux.institutionUniversité de Bordeaux
bordeaux.institutionBordeaux INP
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