CD1 molecule expression on human monocytes induced by granulocyte-macrophage colony-stimulating factor.

W Kasinrerk, T Baumruker, O Majdic… - … (Baltimore, Md.: 1950 …, 1993 - journals.aai.org
W Kasinrerk, T Baumruker, O Majdic, W Knapp, H Stockinger
Journal of immunology (Baltimore, Md.: 1950), 1993journals.aai.org
In this paper we demonstrate that granulocyte-macrophage CSF (GM-CSF) specifically
induces the expression of CD1 molecules, CD1a, CD1b and CD1c, upon human monocytes.
CD1 molecules appeared upon monocytes on day 1 of stimulation with rGM-CSF, and
expression was up-regulated until day 3. Monocytes cultured in the presence of LPS, FMLP,
PMA, recombinant granulocyte-CSF, rIFN-gamma, rTNF-alpha, rIL-1 alpha, rIL-1 beta, and
rIL-6 remained negative. The induction of CD1 molecules by rGM-CSF was restricted to …
Abstract
In this paper we demonstrate that granulocyte-macrophage CSF (GM-CSF) specifically induces the expression of CD1 molecules, CD1a, CD1b and CD1c, upon human monocytes. CD1 molecules appeared upon monocytes on day 1 of stimulation with rGM-CSF, and expression was up-regulated until day 3. Monocytes cultured in the presence of LPS, FMLP, PMA, recombinant granulocyte-CSF, rIFN-gamma, rTNF-alpha, rIL-1 alpha, rIL-1 beta, and rIL-6 remained negative. The induction of CD1 molecules by rGM-CSF was restricted to monocytes, since no such effect was observed upon peripheral blood granulocytes, PBL, and the myeloid cell lines Monomac1, Monomac6, MV4/11, HL60, U937, THP1, KG1, and KG1A. CD1a mRNA was detectable in rGM-CSF-induced monocytes but not in those freshly isolated. SDS-PAGE and immunoblotting analyses of CD1a mAb VIT6 immunoprecipitate from lysate of rGM-CSF-activated monocytes revealed an appropriate CD1a polypeptide band of 49 kDa associated with beta 2-microglobulin. Expression of CD1 molecules on monocytes complements the distribution of these structures on accessory cells, and their specific induction by GM-CSF strengthens the suggestion that CD1 is a family of crucial structures required for interaction between accessory cells and T cells.
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