Suppression of Erythroid but Not Megakaryocytic Differentiation of Human K562 Erythroleukemic Cells by Notch-1

• DOI: 10.1074/jbc.m002866200
• Publication Date: 2002-07-26T14:56:47Z
• Authors: Lloyd T. Lam; Chiara Ronchini; Jason Norton; Anthony J. Capobi...; Emery H. Bresnick
• Keywords: 0301 basic medicine; Erythrocytes; Dose-Response Relationship, Drug; Benzidines; Blotting, Western; Calcium-Binding Proteins; Down-Regulation; Cell Differentiation; Ligands; DNA, Antisense; DNA-Binding Proteins; 03 medical and health sciences; Basic Helix-Loop-Helix Transcription Factors; Erythroid-Specific DNA-Binding Factors; Hemin; Humans; Intercellular Signaling Peptides and Proteins; GATA1 Transcription Factor; Leukemia, Erythroblastic, Acute; K562 Cells; Megakaryocytes; Jagged-1 Protein

The Notch signal transduction pathway is a highly conserved regulatory system that controls multiple developmental processes. We have established an erythroleukemia cell model to study how Notch regulates cell fate and erythroleukemic cell differentiation. K562 and HEL cells expressed the Notch-1 receptor and the Notch ligand Jagged-1. The stable expression of the constitutively active intracellular domain of Notch-1 (NIC-1) in K562 cells inhibited erythroid without affecting megakaryocytic maturation. Expression of antisense Notch-1 induced spontaneous erythroid maturation. Suppression of erythroid maturation by NIC-1 did not result from down-regulation of GATA-1 and TAL-1, transcription factors necessary for erythroid differentiation. Microarray gene expression analysis identified genes activated during erythroid maturation, and NIC-1 disrupted the maturation-dependent changes in the expression of these genes. These results show that NIC-1 alters the pattern of gene expression in K562 cells leading to a block in erythroid maturation and therefore suggest that Notch signaling may control the developmental potential of normal and malignant erythroid progenitor cells.