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HL60

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TheHL-60 cell line is a humanleukemiacell line that has been used for laboratory research on blood cell formation and physiology. HL-60 proliferates continuously in suspensionculture in nutrient andantibiotic chemicals. Thedoubling time is about 36–48 hours. The cell line was derived from a 36-year-old woman who was originally reported to haveacute promyelocytic leukemia at theMD Anderson Cancer Center.[1] HL-60 cells predominantly showneutrophilic promyelocytic morphology.[1] Subsequent evaluation, including the karyotype that showed absence of the defining t(15;17) translocation, concluded that HL-60 cells are from a case of AML FAB-M2 (now referred to as AML with maturation (WHO)).[2]

Proliferation of HL-60 cells occurs through thetransferrin andinsulin receptors, which are expressed on cell surface. The requirement for insulin and transferrin is absolute, as HL-60 proliferation immediately ceases if either of these compounds is removed from the serum-free culture media.[3] With this line, differentiation to maturegranulocytes can be induced by compounds such asdimethyl sulfoxide (DMSO), orretinoic acid. Other compounds like 1,25-dihydroxyvitamin D3,12-O-tetradecanoylphorbol-13-acetate (TPA) andGM-CSF can induce HL-60 to differentiate tomonocytic,macrophage-like andeosinophil phenotypes, respectively.

The HL-60 cultured cell line provides a continuous source of human cells for studying the molecular events of myeloid differentiation and the effects of physiologic, pharmacologic, and virologic elements on this process. HL-60 cell model was used to study the effect ofDNA topoisomerase (topo) IIα and IIβ on differentiation andapoptosis of cells[4] and is especially useful in dielectrophoresis studies,[5] which require an aqueous environment with suspended and round cells. Furthermore, these cells have been used in order to investigate whether intracellularcalcium plays a role incaspase activation induced byreactive oxygen species.[6]

Chromatin and gene expression profiling in HL-60 cells and differentiated cells derived from these has been performed recently.[7]

References

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  1. ^abGallagher R, Collins S, Trujillo J, et al. (1979)."Characterization of the continuous, differentiating myeloid cell line (HL-60) from a patient with acute promyelocytic leukemia".Blood.54 (3):713–733.doi:10.1182/blood.V54.3.713.713.PMID 288488.[permanent dead link]
  2. ^Dalton WT, Jr; Ahearn, MJ; McCredie, KB; Freireich, EJ; Stass, SA; Trujillo, JM (January 1988)."HL-60 cell line was derived from a patient with FAB-M2 and not FAB-M3".Blood.71 (1):242–7.doi:10.1182/blood.V71.1.242.242.PMID 3422031.
  3. ^Breitman, T, S. Collins, B. Keene (1980). "Replacement of serum by insulin and transferrin supports growth and differentiation of the human promyelocytic leukemia cell line, HL-60".Exp. Cell Res.126 (2):494–498.doi:10.1016/0014-4827(80)90296-7.PMID 6988226.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  4. ^Sugimoto, K, K. Yamada, M. Egashira, Y. yazaki, H. Hirai, A. Kikuchi and K. Oshimi (1998)."Temporal and Spatial Distribution of DNA Topoisomerase II Alters During Proliferation, Differentiation, and Apoptosis in HL-60 Cells".Blood.91 (4):1407–1417.doi:10.1182/blood.V91.4.1407.PMID 9454772.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  5. ^Ratanachoo, K., Gascoyne, P.R.C. and Ruchirawat, M. (2002)."Detection of cellular responses to toxicants by dielectrophoresis".Biochim. Biophys. Acta.1564 (2):449–458.doi:10.1016/S0005-2736(02)00494-7.PMC 2726261.PMID 12175928.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  6. ^González D., Bejarano I., Barriga C., Rodríguez A.B., Pariente J.A. (2010)."Oxidative Stress-Induced Caspases are Regulated in Human Myeloid HL-60 Cells by Calcium Signal".Current Signal Transduction Therapy.5 (2):181–186.doi:10.2174/157436210791112172.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  7. ^Teif V.B., Mallm J.P., Sharma T., Mark Welch D.B., Rippe K., Eils R., Langowski J., Olins A.L., Olins D.E. (2017)."Nucleosome repositioning during differentiation of a human myeloid leukemia cell line".Nucleus.8 (2):188–204.doi:10.1080/19491034.2017.1295201.PMC 5403151.PMID 28406749.{{cite journal}}: CS1 maint: multiple names: authors list (link)

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