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Alternative myelomonocytic differentiation of HL-60 reflects dual prospective potency of promyelocytes in human.
- Source :
-
Cellular immunology [Cell Immunol] 1984 Dec; Vol. 89 (2), pp. 385-98. - Publication Year :
- 1984
-
Abstract
- The permanent promyelocytic cell line HL-60 was subjected to stimulation with dimethyl sulfoxide (DMSO) and retinoic acid (RA), as well as 12-O-tetradecanoylphorbol-13-acetate (TPA) and lymphokine conditioned media for the induction of granulocytic or monocytic differentiation, respectively. Cells were investigated cytochemically using alpha-naphthylacetate esterase (acid esterase; AcE), naphthol AS-D chloroacetate esterase, and peroxidase reactions. In addition, the granulocyte or monocyte specific isoenzyme patterns of AcE as an intracytoplasmic property and the immunoreactivity to monoclonal antibodies recognizing granulocytes and monocytes (Ki-M2, Ki-M5) or monocytes alone (Ki-M1) were considered. The results indicated that HL-60 cell line bear the potency to evolve into granulocytes as well as monocytes. Additional studies performed on normal human bone marrow stained for AcE led to the conclusion that the myeloid cell line remains bipolar until the maturation stage of promyelocytes. Myelocytes being AcE positive only in 11.5 +/- 5.0 are heterogeneous and display the first indications of separated monocytic or granulocytic differentiation.
- Subjects :
- Antibodies, Monoclonal
Cell Differentiation drug effects
Cell Line
Concanavalin A
Dimethyl Sulfoxide pharmacology
Esterases analysis
Humans
Immunoenzyme Techniques
Lymphocytes immunology
Lymphokines pharmacology
Peroxidase analysis
Phenotype
Tetradecanoylphorbol Acetate pharmacology
Tretinoin pharmacology
Granulocytes cytology
Leukemia, Myeloid, Acute pathology
Monocytes cytology
Subjects
Details
- Language :
- English
- ISSN :
- 0008-8749
- Volume :
- 89
- Issue :
- 2
- Database :
- MEDLINE
- Journal :
- Cellular immunology
- Publication Type :
- Academic Journal
- Accession number :
- 6096024
- Full Text :
- https://doi.org/10.1016/0008-8749(84)90340-x