Abstract

There are numerous similarities between the erythroid and megakaryocytic lineages which suggest that commitment to either lineage occurs relatively late in hematopoiesis. Commitment toward megakaryocyte development requires obligatory silencing of erythroid-specific genes. Therefore, we investigated the effects of interleukin-6, a known inducer of thrombocyte production, on globin gene expression during erythroid differentiation. Studies in K562 cells demonstrated inhibition of gamma globin gene mRNA production and chain biosynthesis in the presence of exogenous interleukin-6 which was abrogated by anti-interleukin-6 monoclonal antibody. Similar studies in primary erythroid progenitors showed inhibition of burst-forming unit-erythroid colony formation when interleukin-6 was added late in cultures with decreased gamma and beta globin gene mRNA production. Protein binding studies demonstrated an increase in activator protein-1 binding to its consensus sequence by 24 h of interleukin-6 treatment. Inhibition of activator protein-1 gene activity had no effect on gamma gene silencing by interleukin-6. A potential interleukin-6 response element was identified in the gamma globin gene. Interleukin-6 treatment led to a rapid increase in protein binding to the target DNA sequence. These results suggest that interleukin-6 may play an important role in globin gene silencing during megakaryocytic lineage commitment.

Highlights

  • There are numerous similarities between the erythroid and megakaryocytic lineages which suggest that commitment to either lineage occurs relatively late in hematopoiesis

  • During induction of MK development by phorbol esters there is decreased g globin gene expression which occurs through negative regulation of both the rate of production and the stability of g globin mRNA [21]

  • Similar results have been observed with phorbol myristate acetate, which induces the expression of IL-6 and IL-6 receptor (IL-6R) genes in K562 cells [24]

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Summary

Introduction

There are numerous similarities between the erythroid and megakaryocytic lineages which suggest that commitment to either lineage occurs relatively late in hematopoiesis. Similar studies in primary erythroid progenitors showed inhibition of burst-forming unit-erythroid colony formation when interleukin-6 was added late in cultures with decreased g and b globin gene mRNA production. Interleukin-6 treatment led to a rapid increase in protein binding to the target DNA sequence These results suggest that interleukin-6 may play an important role in globin gene silencing during megakaryocytic lineage commitment. At some stage during maturation of the putative bipotential BFUE/MK progenitor cell an additional level of regulation responsible for the proper silencing of globin genes (which are not normally expressed in megakaryocytes) must occur. Gel mobility shift assays (GMSAs) showed increased protein binding to a potential IL-6 response element (IL-6RE) after IL-6 treatment These studies collectively suggest that IL-6 serves as a negative regulator of globin gene expression during megakaryocyte lineage commitment

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