The expression of the glucocorticoid receptor in human erythroblasts is uniquely regulated by KIT Ligand: Implications for stress erythropoiesis Journal Article


Authors: Varricchio, L.; Tirelli, V.; Masselli, E.; Ghinassi, B.; Saha, N.; Besmer, P.; Migliaccio, A. R.
Article Title: The expression of the glucocorticoid receptor in human erythroblasts is uniquely regulated by KIT Ligand: Implications for stress erythropoiesis
Abstract: Studies in mice indicated that activation of the erythroid stress pathway requires the presence of both soluble KIT ligand (KITL) and the glucocorticoid receptor (GR). To clarify the relative role of KITL and GR in stress erythropoiesis in humans, the biological activities of soluble full length-(fl-, 26-190 aa), carboxy-terminus truncated (tr-, 26-162 aa) human (hKITL) and murine (mKITL) KITL in cultures of cord blood (CB) mononuclear cells (MNCs) and CD34pos cells that mimic either steady state (growth factors alone) or stress (growth factors plus dexamethasone [DXM]) erythropoeisis were investigated. In steady state cultures, the KITLs investigated were equally potent in sustaining growth of hematopoietic colonies and expansion of megakaryocytes (MK) and erythroid precursors (EBs). By contrast, under stress erythropoiesis conditions, fl-hKITL generated greater numbers of EBs (fold increase [FI]=140) than tr-hKITL or mKITL (FI=20-40). Flow cytometric analyses indicated that only EBs generated with fl-hKITL remained immature (>70% CD36pos/CD235aneg/low), and therefore capable to proliferate, until day 8-12 in response to DXM. Signaling studies indicated that all KITLs investigated induced EBs to phosphorylate signal transducer and activator of transcription 5 (STAT5) but that extracellular-signaling-regulated- kinases (ERK) activation was observed mainly in the presence of fl-hKITL. EBs exposed to fl-hKITL also expressed higher levels of GRα than those exposed to mKITL (and tr-hKITL) which were reduced upon exposure to the ERK inhibitor U0126. These data reveal a unique requirement for fl-hKITL in the upregulation of GRα and optimal EB expansion in cultures that mimic stress erythropoiesis. © Copyright 2012, Mary Ann Liebert, Inc. 2012.
Keywords: signal transduction; human tissue; protein expression; protein phosphorylation; cell proliferation; phenotype; animals; mice; cells, cultured; cd34 antigen; stem cell factor; erythropoiesis; stress, physiological; phosphorylation; gene expression regulation; protein processing, post-translational; peptide fragments; extracellular signal-regulated map kinases; erythroblasts; upregulation; ex vivo study; stat5 protein; megakaryocyte; protein isoforms; cell expansion; colony forming unit gm; glucocorticoid receptor; receptors, glucocorticoid; megakaryocytes
Journal Title: Stem Cells and Development
Volume: 21
Issue: 15
ISSN: 1547-3287
Publisher: Mary Ann Liebert, Inc  
Date Published: 2012-10-10
Start Page: 2852
End Page: 2865
Language: English
DOI: 10.1089/scd.2011.0676
PROVIDER: scopus
PUBMED: 22533504
PMCID: PMC3623384
DOI/URL:
Notes: --- - "Export Date: 2 January 2013" - "CODEN: SCDTA" - "Source: Scopus"
Altmetric
Citation Impact
BMJ Impact Analytics
MSK Authors
  1. Nayanendu Saha
    23 Saha
  2. Peter Besmer
    115 Besmer