JWA, a novel signaling molecule, involved in the induction of differentiation of human myeloid leukemia cells
pmid: 16430862
JWA, a novel signaling molecule, involved in the induction of differentiation of human myeloid leukemia cells
Dysregulation of hematopoietic cellular differentiation contributes to leukemogenesis. Unfortunately, relatively little is known about how cell differentiation is regulated. JWA (AF070523) is a novel all-trans retinoic acid (ATRA) responsible gene that initially isolated from ATRA-treated primary human tracheal bronchial epithelial cells. For the notable performance achieved by ATRA in the differentiation induction therapy, we investigated the role of JWA in the induction of differentiation of human myeloid leukemia cells. Our results showed that JWA was not only regulated by ATRA but also by several other differentiation inducers such as phorbol-12-myristate-13-acetate (TPA), arabinoside (Ara-C), and hemin, involved in the mechanisms of differentiation along different lineages of myeloid leukemia cells arrested at different stages of development. Generally, JWA was up-regulated by these inducers in a time-dependent manner. Inhibition of JWA by RNA interference decreased the induced cellular differentiation. However, in NB4 cells treated with ATRA, dissimilar with others, the expression of JWA was down-regulated, and the induced cellular differentiation could be enhanced by silencing of JWA. Collectively, JWA works as a potential critical molecule, associated with multi-directional differentiation of human myeloid leukemia cells. In NB4 cells, JWA may function as a lineage-restricted gene during differentiation along the monocyte/macrophage-like or granulocytic pathway.
- University of Arizona United States
- Nanjing Medical University China (People's Republic of)
Macrophages, Blotting, Western, Cell Cycle, Cytarabine, Intracellular Signaling Peptides and Proteins, Membrane Transport Proteins, Bone Marrow Cells, Cell Differentiation, HL-60 Cells, Monocytes, Leukemia, Myeloid, Cell Line, Tumor, Hemin, Humans, RNA Interference, Gene Silencing, K562 Cells, Cells, Cultured, Heat-Shock Proteins, Granulocytes
Macrophages, Blotting, Western, Cell Cycle, Cytarabine, Intracellular Signaling Peptides and Proteins, Membrane Transport Proteins, Bone Marrow Cells, Cell Differentiation, HL-60 Cells, Monocytes, Leukemia, Myeloid, Cell Line, Tumor, Hemin, Humans, RNA Interference, Gene Silencing, K562 Cells, Cells, Cultured, Heat-Shock Proteins, Granulocytes
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