The study of hematopoiesis was greatly facilitated in the mid-1960s when techniques for studying hematopoietic cells in clonal culture were developed. Initially, serum or conditioned medium was added to cultures as a source of growth factors, i.e., the colony-stimulating factors (CSFs) [56, 57, 85]. One of the factors that was isolated, purified, cloned, and produced in commercial quantities was granulocyte colony-stimulating factor (G-CSF), a protein that acts on the neutrophil lineage to selectively stimulate the proliferation and differentiation of committed progenitor cells and activation of mature neutro-phils (Fig. 1). A property that distinguished G-CSF from other CSF and facilitated its purification, molecular cloning, and large-scale production in prokaryotic cells was its ability to induce terminal differentiation of a murine leukemic cell line (WFHI-3B). After observing that serum from endotoxin-treated mice was capable of causing the differentiation of a WFHI-3B myelomono-cytic leukemic cell line, Metcalf [55] named the activity GM-DF (granulocyte-macrophage differentiating factor).
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Foote, M., Morstyn, G. (2009). Granulocyte colony-stimulating factor: biology and clinical potential. In: Oldham, R.K., Dillman, R.O. (eds) Principles of Cancer Biotherapy. Springer, Dordrecht. https://doi.org/10.1007/978-90-481-2289-9_17
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