PHORBOL DIESTER STIMULATED HL-60 CELL DIFFERENTIATION IS ASSOCIATED WITH THE ACTIVATION OF SPECIFIC DNA BINDING PROTEINS (MEETING ABSTRACT) NLM AIDSLINE Important note: Information in this article was accurate in 1991. The state of the art may have changed since the publication date.

Click here to return to AIDSLINE main menu
DonateNow
Print this Article


PHORBOL DIESTER STIMULATED HL-60 CELL DIFFERENTIATION IS ASSOCIATED WITH THE ACTIVATION OF SPECIFIC DNA BINDING PROTEINS (MEETING ABSTRACT)

Proc Annu Meet Am Assoc Cancer Res; 32:A1751 1991. Unique Identifier : AIDSLINE ICDB/91674552
Rogers M; Small GW; Samples L; Daniel LW; Dept. of Biochemistry, Bowman Gray Sch. of Medicine, Wake Forest; Univ., Winston-Salem, NC 27103-2796


Abstract: TPA-stimulated differentiation of HL-60 cells to macrophagelike cells is accompanied by morphological and biochemical changes, including cellular adhesion and expression of the lymphocyte cell adhesion molecule subunit cd 11b. Using cellular adhesion assays and direct immunofluorescence microscopy of cd 11b, we observed a direct correlation between the induction of these markers of macrophage differentiation and the activation of two chloramphenicol acetyl transferase (CAT) reporter plasmids. These plasmids contained sequences upstream of the reporter gene which are activated by the DNA binding proteins NF-kB (HIV-CAT plasmid) and AP-1 (3xTREtkCAT plasmid). HIV-CAT induction began at 24 hr and reached a max expression at 72 hr; 3xTREtkCAT activity started earlier (12 hr) and reached a max earlier (60 hr). TPA (10[-8]M) induced HIV-CAT expression and cellular adhesion was inhibited by the protein kinase C (PKC) inhibitors, ET-18-OCH3, staurosporine, and sphingosine, at nontoxic concentrations. Enhancer-DNA binding protein interactions were also measured in a gel retardation assay. These observations support a role for PKC-mediated gene activation by DNA-binding proteins in HL-60 cell differentiation.
Keywords: Cell Differentiation/DRUG EFFECTS DNA-Binding Proteins/*PHYSIOLOGY Gene Expression Regulation Human Leukemia, Promyelocytic, Acute/*PATHOLOGY Protein Kinase C/PHYSIOLOGY Tetradecanoylphorbol Acetate/*PHARMACOLOGY Tumor Cells, Cultured ABSTRACTKWDcelldifferentiation/drugeffectsdna-bindingproteins/KWDphysiologygeneexpressionregulationhumanleukemia,promyelocytic,acute/KWDpathologyproteinkinasec/physiologytetradecanoylphorbolacetate/KWDpharmacologytumorcells,culturedabstract
910730
M9170999

Copyright © 1991 - National Library of Medicine. Reproduced under license with the National Library of Medicine, Bethesda, MD.

AEGiS is a 501(c)3, not-for-profit, tax-exempt, educational corporation. AEGiS is made possible through unrestricted funding from Boehringer Ingelheim, Bridgestone/Firestone Charitable Trust, Bristol-Myers Squibb Company, Elton John AIDS Foundation, Gill Foundation, the National Library of Medicine, Quest Diagnostics, Roche and Trimeris, and donations from users like you. Always watch for outdated information. This article first appeared in 1991. This material is designed to support, not replace, the relationship that exists between you and your doctor.

AEGiS presents published material, reprinted with permission and neither endorses nor opposes any material. All information contained on this website, including information relating to health conditions, products, and treatments, is for informational purposes only. It is often presented in summary or aggregate form. It is not meant to be a substitute for the advice provided by your own physician or other medical professionals. Always discuss treatment options with a doctor who specializes in treating HIV.

Copyright ©1980, 1991. AEGiS. All materials appearing on AEGiS are protected by copyright as a collective work or compilation under U.S. copyright and other laws and are the property of AEGiS, or the party credited as the provider of the content. .