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A new method to quantify phagocytosis and intracellular degradation using green fluorescent protein‐labeled Escherichia coli : Comparison of cord blood macrophages and peripheral blood macrophages of healthy adults
Author(s) -
Gille Christian,
Spring Baerbel,
Tewes Lena,
Poets Christian F.,
Orlikowsky Thorsten
Publication year - 2006
Publication title -
cytometry part a
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.316
H-Index - 90
eISSN - 1552-4930
pISSN - 1552-4922
DOI - 10.1002/cyto.a.20222
Subject(s) - phagocytosis , green fluorescent protein , escherichia coli , cord blood , intracellular , innate immune system , biology , cd16 , microbiology and biotechnology , cd14 , immune system , immunology , biochemistry , cd8 , gene , cd3
Interactions between innate and adaptive immune functions in neonatal macrophages (MΦ) are still unclear. We therefore established a method to quantify bacterial phagocytosis and intracellular degradation, using green fluorescent protein (GFP)‐labeled Escherichia coli in combination with phenotypic analysis. The kinetics of the proportion of phagocyting MΦ, phagocytosed bacteria per MΦ, and bacterial degradation were comparable for cord blood MΦ of term neonates and MΦ of healthy adults. Phenotyping revealed CD14 and CD16 to be down‐modulated within minutes. GFP‐labeled E. coli may be useful tools to further study MΦ subpopulations and determinants of phagocytosis in cord blood MΦ. © 2006 International Society for Analytical Cytology