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

Blood. 2001 Feb 15;97(4):1016-22. doi: 10.1182/blood.v97.4.1016.

Abstract

Substantial numbers of human mast cells (MCs) were generated from umbilical cord blood (CB) and from adult peripheral blood (PB). A single CB progenitor 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 in terms of high-affinity IgE receptor (FcepsilonRI)-mediated reactions. One million sensitized PB-derived MCs released 3.6 microg histamine, 215 pg IL-5, and 14 ng granulocyte macrophage-colony-stimulating factor (GM-CSF), whereas 10(6) sensitized CB-derived MCs released only 0.8 microg 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. PB-derived MCs highly expressed surface FcepsilonRI alpha chain, and CB-derived MCs almost lacked it in the absence of IgE. PB-derived MCs expressed approximately 5 times higher levels of messenger RNA (mRNA) for FcepsilonRI alpha chain than CB-derived MCs, but mRNAs for beta and gamma chains of the receptors were equally expressed. Among the approximately 5600 kinds of full-length human genes examined by using the high-density oligonucleotide probe-array system, FcepsilonRIalpha was ranked the fifth most increased transcript in PB-derived MCs. 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 FcepsilonRIalpha transcription, which is probably committed at progenitor stages and is, at least in part, cytokine-insensitive.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aging / genetics
  • Aging / metabolism
  • Blood Cells / cytology*
  • Blood Cells / drug effects
  • Blood Cells / metabolism
  • Calcimycin / pharmacology
  • Calcium Signaling / drug effects
  • Cells, Cultured
  • Culture Media, Serum-Free
  • Down-Regulation* / drug effects
  • Fetal Blood / cytology*
  • Fetal Blood / drug effects
  • Gene Expression Profiling
  • Granulocyte-Macrophage Colony-Stimulating Factor / metabolism
  • Histamine Release
  • Humans
  • Infant, Newborn
  • Interleukin-5 / metabolism
  • Ionophores / pharmacology
  • Mast Cells / cytology*
  • Mast Cells / drug effects
  • Mast Cells / metabolism
  • Oligonucleotide Array Sequence Analysis
  • Organ Specificity
  • RNA, Messenger / biosynthesis*
  • RNA, Messenger / genetics
  • Receptors, IgE / biosynthesis*
  • Receptors, IgE / chemistry
  • Receptors, IgE / genetics
  • Transcription, Genetic / drug effects

Substances

  • Culture Media, Serum-Free
  • Interleukin-5
  • Ionophores
  • RNA, Messenger
  • Receptors, IgE
  • Calcimycin
  • Granulocyte-Macrophage Colony-Stimulating Factor