Lmo2 Induces Hematopoietic Stem Cell-Like Features in T-Cell Progenitor Cells Prior to Leukemia

SM Cleveland, S Smith, R Tripathi, EM Mathias… - Stem Cells, 2013 - academic.oup.com
SM Cleveland, S Smith, R Tripathi, EM Mathias, C Goodings, N Elliott, D Peng, W El-Rifai
Stem Cells, 2013academic.oup.com
Abstract LIM domain only 2 (Lmo2) is frequently deregulated in sporadic and gene therapy-
induced acute T-cell lymphoblastic leukemia (T-ALL) where its overexpression is an
important initiating mutational event. In transgenic and retroviral mouse models, Lmo2
expression can be enforced in multiple hematopoietic lineages but leukemia only arises
from T cells. These data suggest that Lmo2 confers clonal growth advantage in T-cell
progenitors. We analyzed proliferation, differentiation, and cell death in CD2-Lmo2 …
Abstract
LIM domain only 2 (Lmo2) is frequently deregulated in sporadic and gene therapy-induced acute T-cell lymphoblastic leukemia (T-ALL) where its overexpression is an important initiating mutational event. In transgenic and retroviral mouse models,  Lmo2  expression can be enforced in multiple hematopoietic lineages but leukemia only arises from T cells. These data suggest that  Lmo2  confers clonal growth advantage in T-cell progenitors. We analyzed proliferation, differentiation, and cell death in  CD2-Lmo2  transgenic thymic progenitor cells to understand the cellular effects of enforced  Lmo2  expression. Most impressively,  Lmo2  transgenic T-cell progenitor cells were blocked in differentiation, quiescent, and immortalized in vitro on OP9-DL1 stromal cells. These cellular effects were concordant with a transcriptional signature in  Lmo2  transgenic T-cell progenitor cells that is also present in hematopoietic stem cells (HSCs) and early T-cell precursor ALL. These results are significant in light of the crucial role of  Lmo2  in the maintenance of the HSC. The cellular effects and transcriptional effects have implications for LMO2-dependent leukemogenesis and the treatment of  LMO2-induced T-ALL.
Oxford University Press