Biophysical investigation of living monocytes in flow by collaborative coherent imaging techniques

被引:22
作者
Dannhauser, David [1 ]
Rossi, Domenico [1 ]
Memmolo, Pasquale [2 ]
Finizio, Andrea [2 ]
Ferraro, Pietro [2 ]
Netti, Paolo Antonio [1 ,3 ,4 ]
Causa, Filippo [1 ,3 ,4 ]
机构
[1] Ist Italiano Tecnol, Ctr Adv Biomat Hlth Care CRIB, Largo Barsanti & Matteucci 53, I-80125 Naples, Italy
[2] CNR ISASI Inst Appl Sci & Intelligent Syst E Caia, Via Campi Flegrei 34, I-80078 Pozzuoli, Italy
[3] Univ Napoli Federico II, Interdisciplinary Res Ctr Biomat CRIB, Piazzale Tecchio 80, I-80125 Naples, Italy
[4] Univ Napoli Federico II, Dipartimento Ingn Chim Mat & Prod Ind DICMAPI, Piazzale Tecchio 80, I-80125 Naples, Italy
关键词
LIGHT-SCATTERING; BLOOD-CELLS; CLASSIFICATION; SIZE;
D O I
10.1364/BOE.9.005194
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
We implemented a completely label-free biophysical (morphometric and optical) property characterization of living monocytes in flow, using measurements obtained from two coherent imaging techniques: a pure light scattering approach to obtain an optical signature (OS) of cells, and a digital holography (DH) approach to achieve optical cell reconstructions in flow. A precise 3D cell alignment platform, taking advantage of viscoelastic fluid properties and microfluidic channel geometry, was used to investigate the OS of cells to achieve their refractive index, ratio of the nucleus over cytoplasm, and overall cell dimension. Further quantitative phase-contrast reconstructions by DH were employed to calculate surface area, dry mass, and biovolume of monocytes by using the OS outcomes as input parameters. The results show significantly different biophysical cell properties, confirming the possibility to differentiate monocytes from other cell classes in flow, thus avoiding chemical cell staining or labeling, which are nowadays used. (C) 2018 Optical Society of America under the terms of the OSA Open Access Publishing Agreement
引用
收藏
页码:5194 / 5204
页数:11
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