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PMID: 29601874 Published · ppublish English Journal Article Research Support, N.I.H., Extramural

Isolating the influences of fluid dynamics on selectin-mediated particle rolling at venular junctional regions.

Microvascular research ·Vol. 118 ·2018-00-00 ·页码 144-154

Jung JJ, Grayson KA, King MR, Lamkin-Kennard KA

Abstract

The objective of this study was to isolate the impact of hydrodynamics on selectin-mediated cell rolling in branched microvessels. Significant advancements have been made in furthering the understanding of complex interactions between biochemical and physical factors in the inflammatory cascade in simplified planar geometries. However, few studies have sought to quantify the effects of branched configurations and to isolate the effects of associated fluid forces. Experimental techniques were developed to perform in vitro adhesion experiments in Y-shaped micro-slides. The micro-slides were coated with P-selectin and microspheres coated with Sialyl-Lewisx were observed as they rolled in the chambers at different wall shear stresses. Study results revealed that microsphere rolling velocities and rolling flux were lowest in regions closest to the apex of a junctional region and were dependent on both branch angle and wall shear stress. The regions closest to the junctional region were shown to have low bulk flow velocities and shear stresses using computational fluid dynamics (CFD) modeling. Collectively, the study demonstrates that despite the presence of a uniform coating of P-selectin, hydrodynamic factors associated with the chamber geometry yield non-uniform effects on particle behavior. These findings could explain why cells have been observed to preferentially adhere or transmigrate near junctional regions. Future characterization of inflammatory processes in microvascular network configurations is therefore crucial for furthering our fundamental understanding of inflammation.

Keywords
Hydrodynamics Inflammation Microcirculation Neutrophil rolling
MeSH 主题词
Animals Cell Adhesion Humans Hydrodynamics Inflammation/metabolism,pathology Leukocyte Rolling Leukocytes/metabolism Lewis X Antigen/metabolism Microspheres Models, Cardiovascular P-Selectin/metabolism Sialyl Lewis X Antigen Signal Transduction Venules/metabolism,pathology
化学物质
Lewis X Antigen P-Selectin Sialyl Lewis X Antigen
作者与单位
共 4 位作者,点击展开单位 / ORCID
Jung John J
Rochester Institute of Technology, Rochester, NY, United States.
Grayson Korie A
Cornell University, Ithaca, NY, United States.
King Michael R
Vanderbilt University, Nashville, TN, United States.
Lamkin-Kennard Kathleen A
Rochester Institute of Technology, Rochester, NY, United States. Electronic address: [email protected].
Article Info
Journal
Microvascular research
Abbr.
Microvasc Res
ISSN
1095-9319
Corresponding email
Published
2018-00-00
电子出版
2018-00-27
页码
144-154
Language
English
Country/Region
United States
NLM ID
0165035
基金资助
NHLBI NIH HHS · R15 HL088685 · United States
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