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Monocyte CD64 or CD89 targeting by surfactant protein D/anti‐Fc receptor mediates bacterial uptake
Author(s) -
Tacken Paul J.,
Batenburg Joseph J.
Publication year - 2006
Publication title -
immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.297
H-Index - 133
eISSN - 1365-2567
pISSN - 0019-2805
DOI - 10.1111/j.1365-2567.2006.02324.x
Subject(s) - cd64 , u937 cell , receptor , fc receptor , internalization , biology , microbiology and biotechnology , monocyte , fusion protein , cell culture , recombinant dna , immunology , biochemistry , gene , genetics
Summary We recently showed that a chimeric protein, consisting of a recombinant fragment of human surfactant protein D (rfSP‐D) coupled to a Fab′ fragment directed against the human Fcα receptor (CD89), effectively targets pathogens recognized by SP‐D to human neutrophils. The present study evaluates the effectiveness of chimeric rfSP‐D/anti‐Fc receptor proteins targeting Escherichia coli to CD89 or to the Fcγ receptor I (CD64) on monocytes. Both chimeric rfSP‐D/anti‐Fc receptor proteins increased internalization of E. coli by the human promonocytic cell line U937, but only after induction of monocytic differentiation, despite the fact that the expression levels of CD64 and CD89 on undifferentiated cells were at least as high as on differentiated cells. The two chimeric rfSP‐D/anti‐Fc receptor proteins did not enhance each other's effect on E. coli uptake. Targeting to differentiated U937 cells was inhibited by blocking the interaction either between the rfSP‐D part of the chimeric molecule and E. coli , or between the anti‐Fc receptor Fab′ fragment and the Fc receptor on the U937 cell. In conclusion, both CD64 and CD89 on U937 cells prove to be suitable for targeting by rfSP‐D/anti‐Fc receptor proteins. However, in addition to mere Fc receptor expression, effective targeting requires monocytic differentiation.