3.8 Article Proceedings Paper

Plug flow cytometry extends analytical capabilities in cell adhesion and receptor pharmacology

期刊

CYTOMETRY
卷 43, 期 3, 页码 211-216

出版社

WILEY-LISS
DOI: 10.1002/1097-0320(20010301)43:3<211::AID-CYTO1052>3.0.CO

关键词

flow cytometry; automation; sample handling; cell adhesion

资金

  1. NCRR NIH HHS [RR14175, RR01315] Funding Source: Medline
  2. NHLBI NIH HHS [HL56384] Funding Source: Medline

向作者/读者索取更多资源

Background: Plug flow cytometry is a recently developed system for the automated delivery of multiple small boluses or plugs of cells or particles to the flow cytometer for analysis. Important system features are that sample plugs are of precisely defined volume and that the sample vessel need not be pressurized. We describe how these features enable direct cell concentration determinations and novel ways to integrate flow cytometers with other analytical instruments. Methods: Adhesion assays employed human polymorphonuclear neutrophils (PMNs) loaded with Fura Red and Chinese hamster ovary (CHO) cells cotransfected with genes for green fluorescent protein (GFP) and human P-selectin. U937 cells expressing the human 7-transmembrane formyl peptide receptor were loaded with the fluorescent probe indo-1 for intracellular ionized calcium determinations. A computer-controlled syringe or peristaltic pump loaded the sample into a sample loop of the plug now coupler, a reciprocating eight-port valve. When the valve position was switched, the plug of sample in the sample loop was transported to the flow cytometer by a pressure-driven fluid line. Results: In stirred mixtures of PMNs and CHO cells, we used plug flow cytometry to directly quantify changes in concentrations of nonadherent singlet PMNs. This approach enabled accurate quantification of adherent PMNs in multicell aggregates. We constructed a novel plug flow interface between the flow cytometer and a cone-plate viscometer to enable real-time flow cytometric analysis of cell-cell adhesion under conditions of uniform shear. The High Throughput Pharmacology System (HTPS) is an instrument used for automated programming of complex pharmacological cell treatment protocols. It was interfaced via the plug flow coupling device to enable rapid (<5 min) flow cytometric characterization of the intracellular calcium dose-response profile of U937 cells to formyl peptide. Conclusions: By facilitating the coupling of flow cytometers to other fluidics-based analytical instruments, plug flow cytometry has extended analytical capabilities in cell adhesion and pharmacological characterization of receptor-ligand interactions.

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