Different Blocks in the Differentiation of Myeloid Leukemic Cells
AUTOR(ES)
Lotem, Joseph
RESUMO
Some clones of mouse myeloid leukemic cells (D+) can be induced to undergo cell differentiation to mature macrophages and granulocytes, and other clones (D-) could not be induced to differentiate to mature cells. Normal mature macrophages and granulocytes have surface receptors that form rosettes with erythrocytes coated with specific immunoglobulin or immunoglobulin-complement. The D+ clones were induced to form receptors by prednisolone, cytosine-arabinoside, 5-iododeoxyuridine, actinomycin D, or serum from mice injected with endotoxin. All these compounds thus induced a common change in the cell surface membrane. The induction of receptors required protein synthesis, and receptors were formed before the appearance of mature cells. There were two types of D- clones. One type was induced by these compounds to form receptors, although with a lower inducibility than D+ clones; in the other type there was no induction of receptors. The results indicate that there are different blocks in the differentiation of myeloid leukemic cells. Some leukemic cells (IR+D+) can be induced to form receptors and to differentiate to mature cells; others (IR+D-) can form receptors but not mature cells; and a third type (IR-D-) could not be induced to form receptors or mature cells.
ACESSO AO ARTIGO
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=433803Documentos Relacionados
- Genetic dissection of the control of normal differentiation in myeloid leukemic cells
- Indirect induction of differentiation in myeloid leukemic cells by lipid A
- Membrane differentiation in human myeloid cells: expression of unique profiles of cell surface glycoproteins in myeloid leukemic cell lines blocked at different stages of differentiation and maturation.
- Chromosome mapping of the genes that control differentiation and malignancy in myeloid leukemic cells.
- Control of Normal Differentiation of Myeloid Leukemic Cells to Macrophages and Granulocytes