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BAALC, a novel marker of human hematopoietic progenitor cells
- Source :
-
Experimental Hematology . Nov2003, Vol. 31 Issue 11, p1051. 6p. - Publication Year :
- 2003
-
Abstract
- : ObjectiveThe gene BAALC (Brain And Acute Leukemia, Cytoplasmic), a novel molecular marker involved in leukemia, is highly expressed in a subset of patients with acute leukemia and predictive of clinical outcome in patients with acute myeloid leukemia and normal karyotype. The role of BAALC in hematopoiesis and leukemogenesis is unknown.: Material and methodsWe used real-time RT-PCR to show that BAALC is strongly expressed in CD34+ cells from the bone marrow and blood and only weakly expressed in total normal bone marrow and blood cells.: ResultsExpression analyses of FACSorted cells revealed high BAALC transcript levels in CD34+ bone marrow cells including CD34+/CD38−, CD34+/CD33+, as well as CD34+/CD19+/CD10+, CD34+/CD7+, and CD34+/CD71+/CD45− cell fractions. Expression was significantly lower in all CD34− fractions. In vitro differentiation of CD34+ bone marrow cells showed downregulation of BAALC and CD34 transcripts as early as day 4 in suspension cultures supplemented with lineage-specific cytokines (G-CSF, M-CSF, or EPO). In cultures with only lineage-unspecific cytokines (IL-3, SCF, GM-CSF), BAALC transcripts persisted up to day 20, while CD34 transcripts disappeared earlier. These observations suggest that expression of BAALC is stage specific.: ConclusionsBAALC expression is restricted to progenitor cells, and downregulation of BAALC occurs with cell differentiation. We postulate that BAALC represents a novel marker of an early progenitor cell common to the myeloid, lymphoid, and erythroid pathways. [Copyright &y& Elsevier]
- Subjects :
- *ACUTE myeloid leukemia
*BLOOD cells
*CLINICAL pathology
*HEMATOPOIESIS
Subjects
Details
- Language :
- English
- ISSN :
- 0301472X
- Volume :
- 31
- Issue :
- 11
- Database :
- Academic Search Index
- Journal :
- Experimental Hematology
- Publication Type :
- Academic Journal
- Accession number :
- 11175918
- Full Text :
- https://doi.org/10.1016/j.exphem.2003.08.004