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Title: PU.1 silencing leads to terminal differentiation of erythroleukemia cells

Journal Article · · Biochemical and Biophysical Research Communications
 [1];  [1]
  1. Department of Biotechnology and Food Engineering, Technion-Israel Institute of Technology, Haifa 32000 (Israel)

The transcription factor PU.1 plays a central role in development and differentiation of hematopoietic cells. Evidence from PU.1 knockout mice indicates a pivotal role for PU.1 in myeloid lineage and B-lymphocyte development. In addition, PU.1 is a key player in the development of Friend erythroleukemia disease, which is characterized by proliferation and differentiation arrest of proerythrocytes. To study the role of PU.1 in erythroleukemia, we have used murine erythroleukemia cells, isolated from Friend virus-infected mice. Expression of PU.1 small interfering RNA in these cells led to significant inhibition of PU.1 levels. This was accompanied by inhibition of proliferation and restoration in the ability of the proerythroblastic cells to produce hemoglobin, i.e., reversion of the leukemic phenotype. The data suggest that overexpression of PU.1 gene is the immediate cause for maintaining the leukemic phenotype of the disease by retaining the self-renewal capacity of transformed erythroblastic cells and by blocking the terminal differentiation program towards erythrocytes.

OSTI ID:
20709151
Journal Information:
Biochemical and Biophysical Research Communications, Vol. 329, Issue 4; Other Information: DOI: 10.1016/j.bbrc.2005.02.109; PII: S0006-291X(05)00317-7; Copyright (c) 2005 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved; Country of input: International Atomic Energy Agency (IAEA); ISSN 0006-291X
Country of Publication:
United States
Language:
English