DocumentCode
386542
Title
Fluid shear modulates the molecular interactions between polymorphonuclear leukocytes and colon carcinomas
Author
Jadhav, S. ; Konstantopoulos, K.
Author_Institution
Dept. of Chem. Eng., Johns Hopkins Univ., Baltimore, MD, USA
Volume
1
fYear
2002
fDate
2002
Firstpage
734
Abstract
This study compares the kinetics, adhesion efficiency, and molecular requirements of polymorphonuclear leukocyte (PMN) binding to two colon adenocarcinoma cell-lines, the ICAM-1-negative/sLex-bearing LS174T and the ICAM-1-expressing/sLex-low HCT-8 as a function of hydrodynamic shear rate (50-1600 sec-1). The efficiency of both PMN homotypic and PMN-colon carcinoma heterotypic interactions, defined as the fraction of collisions between respective cells that result in aggregation, decreases sharply at low shear. At higher shear, PMN homotypic efficiency remains relatively unchanged, while heterotypic efficiencies continue to decrease with PMN binding to LS174T cells being more efficient than to HCT-8 cells. The relative contributions of LFA-1 and Mac-1 as well as their respective ligands on HCT-8 cells to heterotypic aggregation were investigated in the presence of fluid shear.
Keywords
adhesion; aggregation; blood; blood vessels; cell motility; cellular biophysics; molecular biophysics; tumours; HCT-8 cells; ICAM-1; LFA-1; LS174T cells; Mac-1; PMN binding; PMN homotypic interactions; PMN-colon carcinoma heterotypic interactions; adhesion efficiency; aggregation; blood-borne metastasis; cell-cell interactions; collisions; colon adenocarcinoma cell-lines; colon carcinomas; fluid shear; heterotypic efficiencies; homotypic efficiency; hydrodynamic shear rate; kinetics; ligands; molecular interactions; polymorphonuclear leukocyte binding; vasculature; Adhesives; Aggregates; Chemical engineering; Colon; Humans; Hydrodynamics; Kinetic theory; Metastasis; Tumors; White blood cells;
fLanguage
English
Publisher
ieee
Conference_Titel
Engineering in Medicine and Biology, 2002. 24th Annual Conference and the Annual Fall Meeting of the Biomedical Engineering Society EMBS/BMES Conference, 2002. Proceedings of the Second Joint
ISSN
1094-687X
Print_ISBN
0-7803-7612-9
Type
conf
DOI
10.1109/IEMBS.2002.1137043
Filename
1137043
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