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• W166477881 abstract "There are clones of myeloid leukemic cells which are different from normal myeloid cells in that they have become independent of hematopoietic growth factor for cell viability and growth. The ability of these clones to bind three types of hematopoietic growth factors (MGI-1GM = GM-CSF, IL-3 = multi-CSF and MGI-1M = M-CSF = CSF-1) was measured using the method of quantitative absorption at 1 degree C and low pH elution of cell-bound biological activity. Results of binding to normal myeloid and lymphoid cells were similar to those obtained by radioreceptor assays. The results indicate that the number of receptors on different clones of these leukemic cells varied from 0 to 1,300 per cell. The receptors have a high binding affinity. Receptors for different growth factors can be independently expressed in different clones. There was no relationship between expression of receptors for these growth factors and the phenotype of the leukemic cells regarding their ability to be induced to differentiate. The number of receptors on the leukemic cells was lower than on normal mature macrophages. Myeloid leukemic cells induced to differentiate by normal myeloid cell differentiation factor MGI-2 (= DF), or by low doses of actinomycin D or cytosine arabinoside, showed an up-regulation of the number of MGI-1GM and IL-3 receptors. Induction of differentiation of leukemic cells by MGI-2 also induced production and secretion of the growth factor MGI-1GM, and this induced MGI-1GM saturated the up-regulated MGI-1GM receptors. It is suggested that up-regulation of these receptors during differentiation is required for the functioning of differentiated cells." @default.
• W166477881 created "2016-06-24" @default.
• W166477881 creator A5000036288 @default.
• W166477881 creator A5057501504 @default.
• W166477881 date "1986-09-01" @default.
• W166477881 modified "2023-10-12" @default.
• W166477881 title "Regulation of cell surface receptors for different hematopoietic growth factors on myeloid leukemic cells." @default.
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• W166477881 doi "https://doi.org/10.1002/j.1460-2075.1986.tb04480.x" @default.
• W166477881 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/1167096" @default.
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