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PMID: 6260353 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Functionally deficient differentiation of HL-60 promyelocytic leukemia cells induced by phorbol myristate acetate.

Cancer research ·Vol. 41 ·No. 5 ·1981-05-00 ·Pages 1861-5

Newburger PE, Baker RD, Hansen SL, Duncan RA, Greenberger JS

Abstract

The human promyelocytic leukemia cell line HL-60 undergoes terminal myeloid differentiation in vitro in response to a wide variety of chemicals. The tumor promoter phorbol myristate acetate induces these cells to develop macrophage-like morphology, adherence, and enzymatic characteristics. The present study confirms those observations and further documents the induction, by 16 nM phorbol myristate acetate, of 5'-nucleotidase activity, another human macrophage marker enzyme. However, more importantly, functional studies show that phorbol myristate acetate-induced HL-60 cells fail to increase above base line uninduced levels of hexose monophosphate shunt activity, superoxide generation, nitroblue tetrazolium reduction, bacterial ingestion, or complement secretion. These cells therefore possess some macrophage-like properties but do not meet several important functional criteria of macrophage identity.

MeSH Terms
Cell Differentiation/drug effects Complement System Proteins/metabolism Humans Leukemia, Myeloid, Acute/pathology Macrophages/pathology,physiology Nucleotidases/metabolism Oxygen Consumption Phagocytosis Phorbols/pharmacology Tetradecanoylphorbol Acetate/pharmacology
Chemicals
Phorbols Complement System Proteins Nucleotidases Tetradecanoylphorbol Acetate
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Newburger P E
Baker R D
Hansen S L
Duncan R A
Greenberger J S
Article Info
Journal
Cancer research
Abbr.
Cancer Res
ISSN
0008-5472
Published
1981-05-00
Pages
1861-5
Language
English
Region
United States
NLM ID
2984705R
Subset
IM
Grants
NIADDK NIH HHS · 5-T32-AM-07333 · United States
NCI NIH HHS · CA-26033 · United States
NCI NIH HHS · CA-26506 · United States
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