Selective down-regulation of high-affinity IgE receptor (Fc epsilon RI) alpha-chain messenger RNA among transcriptome in cord blood-derived versus adult peripheral blood-derived cultured human mast cells

Citation
M. Iida et al., Selective down-regulation of high-affinity IgE receptor (Fc epsilon RI) alpha-chain messenger RNA among transcriptome in cord blood-derived versus adult peripheral blood-derived cultured human mast cells, BLOOD, 97(4), 2001, pp. 1016-1022
Citations number
29
Categorie Soggetti
Hematology,"Cardiovascular & Hematology Research
Journal title
BLOOD
ISSN journal
00064971 → ACNP
Volume
97
Issue
4
Year of publication
2001
Pages
1016 - 1022
Database
ISI
SICI code
0006-4971(20010215)97:4<1016:SDOHIR>2.0.ZU;2-0
Abstract
Substantial numbers of human mast cells (MCs) were generated from umbilical cord blood (CB) and from adult peripheral blood (PB). A single CB progenit or produced 15 436 MCs, whereas a single PB progenitor produced 807 MCs on average. However, PB-derived MCs were far more active than CB-derived MCs i n terms of high-affinity IgE receptor (Fc epsilon RI)-mediated reactions. O ne million sensitized PB-derived MCs released 3.6 mug histamine, 215 pg IL- 5, and 14 ng granulocyte macrophage-colony-stimulating factor (GMCSF), wher eas 10(6) sensitized CB-derived MCs released only 0.8 mug histamine, 31 pg IL-5, and 0.58 ng GM-CSF on anti-IgE challenge. However, ionophore A23 187 released similar levels of histamine from the 2 MC types. PR-derived MCs hi ghly expressed surface FceRI alpha chain, and CB-derived MCs almost lacked it in the absence of IgE, PR-derived MCs expressed approximately 5 times hi gher levels of messenger RNA (mRNA) for Fc epsilon RI a chain than CB-deriv ed MCs, but mRNAs for beta and gamma chains of the receptors were equally e xpressed. Among the approximately 5600 kinds of full-length human genes exa mined by using the high-density oligonucleotide probe-array system, Fc epsi lon RI alpha was ranked the fifth most increased transcript in PB-derived M Cs, The 4 other increased transcripts were unrelated to MC function. These results suggest that IgE-mediated reactions may be restricted during early infancy through the selective inhibition of Fc epsilon RI alpha transcripti on, which is probably committed at progenitor stages and is, at least in pa rt, cytokine-insensitive. (C) 2001 by The American Society of Hematology.