Literature DB >> 21141947

Examining the lateral displacement of HL60 cells rolling on asymmetric P-selectin patterns.

Chia-Hua Lee1, Suman Bose, Krystyn J Van Vliet, Jeffrey M Karp, Rohit Karnik.   

Abstract

The lateral displacement of cells orthogonal to a flow stream by rolling on asymmetrical receptor patterns presents a new opportunity for the label-free separation and analysis of cells. Understanding the nature of cell rolling trajectories on such substrates is necessary to the engineering of substrates and the design of devices for cell separation and analysis. Here, we investigate the statistical nature of cell rolling and the effect of pattern geometry and flow shear stress on cell rolling trajectories using micrometer-scale patterns of biomolecular receptors with well-defined edges. Leukemic myeloid HL60 cells expressing the PSGL-1 ligand were allowed to flow across a field of patterned lines fabricated using microcontact printing and functionalized with the P-selectin receptor, leveraging both the specific adhesion of this ligand-receptor pair and the asymmetry of the receptor pattern inclination angle with respect to the fluid shear flow direction (α = 5, 10, 15, and 20°). The effects of the fluid shear stress magnitude (τ = 0.5, 1, 1.5, and 2.0 dyn/cm(2)), α, and P-selectin incubation concentration were quantified in terms of the rolling velocity and edge tracking length. Rolling cells tracked along the inclined edges of the patterned lines before detaching and reattaching on another line. The detachment of rolling cells after tracking along the edge was consistent with a Poisson process of history-independent interactions. Increasing the edge inclination angle decreased the edge tracking length in an exponential manner, contrary to the shear stress magnitude and P-selectin incubation concentration, which did not have a significant effect. On the basis of these experimental data, we constructed an empirical model that predicted the occurrence of the maximum lateral displacement at an edge angle of 7.5°. We also used these findings to construct a Monte Carlo simulation for the prediction of rolling trajectories of HL60 cells on P-selectin-patterned substrates with a specified edge inclination angle. The prediction of lateral displacement in the range of 200 μm within a 1 cm separation length supports the feasibility of label-free cell separation via asymmetric receptor patterns in microfluidic devices.

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Year:  2010        PMID: 21141947      PMCID: PMC3068857          DOI: 10.1021/la102871m

Source DB:  PubMed          Journal:  Langmuir        ISSN: 0743-7463            Impact factor:   3.882


  35 in total

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Journal:  Biophys J       Date:  2000-10       Impact factor: 4.033

Review 5.  Microengineering of cellular interactions.

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7.  Activation of human leukocytes reduces surface P-selectin glycoprotein ligand-1 (PSGL-1, CD162) and adhesion to P-selectin in vitro.

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9.  Microcontact printing of P-selectin increases the rate of neutrophil recruitment under shear flow.

Authors:  Dooyoung Lee; Michael R King
Journal:  Biotechnol Prog       Date:  2008 Sep-Oct

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Authors:  Tadayuki Yago; Anne Leppänen; Haiying Qiu; Warren D Marcus; Matthias U Nollert; Cheng Zhu; Richard D Cummings; Rodger P McEver
Journal:  J Cell Biol       Date:  2002-08-12       Impact factor: 10.539

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7.  Studying cell rolling trajectories on asymmetric receptor patterns.

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9.  Affinity flow fractionation of cells via transient interactions with asymmetric molecular patterns.

Authors:  Suman Bose; Rishi Singh; Mikhail Hanewich-Hollatz; Chong Shen; Chia-Hua Lee; David M Dorfman; Jeffrey M Karp; Rohit Karnik
Journal:  Sci Rep       Date:  2013       Impact factor: 4.379

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