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PMID: 9458106 Published · ppublish English Comparative Study Journal Article Research Support, Non-U.S. Gov't

Enforced TAL-1 expression stimulates primitive, erythroid and megakaryocytic progenitors but blocks the granulopoietic differentiation program.

Cancer research ·Vol. 58 ·No. 3 ·1998-02-01 ·Pages 562-9

Valtieri M, Tocci A, Gabbianelli M, Luchetti L, Masella B, Vitelli L, Botta R, Testa U, Condorelli GL, Peschle C

Abstract

In human adult hematopoiesis, the TAL-1 gene is up- and down-modulated in erythropoiesis and granulopoiesis, respectively [G. L. Condorelli et al., Blood, 86: 164-175, 19951. Here, it is shown that, in a hematopoietic progenitor cell (HPC) unilineage differentiation culture, tal-1 is induced and then expressed, in a sustained manner, in the megakaryopoietic lineage, whereas it is barely or not detected in the monocytopoietic series. We have investigated the role of enforced tal-1 expression by retroviral transfer into HPCs [erythroid burst-forming units and megakaryocytic and granulomonocytic colony-forming units (CFUs)], primitive HPCs (high proliferative potential colony-forming cells), and putative hematopoietic stem cells (HSCs), assayed as long-term culture initiating cells. TAL-1 overexpression induces an increase of erythroid burst-forming unit colony number and size and megakaryocytic CFU colony number and an inhibition of granulomonocytic CFU and granulocytic CFU (CFU-G) but not monocytic CFU colony number; conversely, TAL-1 mutants with defective heterodimerizing or DNA-binding domains do not exert these effects at a significant level. Although it does not affect long-term culture initiating cells, exogenous TAL-1 causes a significant proliferative stimulus on primary and secondary high proliferative potential colony-forming cells. In conclusion, exogenous tal-1 exerts differential and stage- and lineage-specific effects on the HPC/HSC differentiation/proliferation gene programs. Thus, it induces a stimulatory effect at the level of erythroid and megakaryocytic HPCs, while exerting a selective proliferative action on downstream erythropoiesis. Furthermore, it induces differential effects on the myeloid series: the partial blockade of CFU-G differentiation is possibly linked to the sharp down-modulation of endogenous TAL-1 expression at the level of the CFU-G-to-granulopoietic precursor differentiation step; in contrast, no significant effect is observed on monocytic CFU colony formation. Finally, the stimulatory effect on primitive HPCs but not putative stem cells suggests subtle differences in the effects exerted by tal-1 overexpression on primitive HPC/HSC subsets in adult life.

MeSH Terms
Adult Basic Helix-Loop-Helix Transcription Factors Cell Differentiation/drug effects Cell Lineage Cells, Cultured Colony-Forming Units Assay Culture Media Culture Techniques/methods DNA-Binding Proteins/genetics,physiology Erythroid Precursor Cells/cytology,drug effects Erythropoiesis/drug effects Fibroblast Growth Factor 2/pharmacology Genetic Vectors/genetics Granulocytes/cytology,drug effects Hematopoiesis/drug effects Hematopoietic Cell Growth Factors/pharmacology Hematopoietic Stem Cells/cytology,drug effects Humans Interleukins/pharmacology Megakaryocytes/cytology,drug effects Proto-Oncogene Proteins Recombinant Fusion Proteins/physiology Recombinant Proteins/pharmacology Retroviridae/genetics T-Cell Acute Lymphocytic Leukemia Protein 1 Transcription Factors Transfection
Chemicals
Basic Helix-Loop-Helix Transcription Factors Culture Media DNA-Binding Proteins Hematopoietic Cell Growth Factors Interleukins Proto-Oncogene Proteins Recombinant Fusion Proteins Recombinant Proteins T-Cell Acute Lymphocytic Leukemia Protein 1 Transcription Factors Fibroblast Growth Factor 2 TAL1 protein, human
Authors & Affiliations
10 authors, click to expand affiliations / ORCID
Valtieri M
Department of Hematology and Oncology, Istituto Superiore di Sanità, Rome, Italy.
Tocci A
Gabbianelli M
Luchetti L
Masella B
Vitelli L
Botta R
Testa U
Condorelli G L
Peschle C
Article Info
Journal
Cancer research
Abbr.
Cancer Res
ISSN
0008-5472
Published
1998-02-01
Pages
562-9
Language
English
Region
United States
NLM ID
2984705R
Subset
IM
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