Establishment of an activated macrophage cell line, A-THP-1, and its properties

Tohoku J Exp Med. 1998 Oct;186(2):99-119. doi: 10.1620/tjem.186.99.

Abstract

A new macrophage cell line with activated character and unique morphology was isolated by selecting adherent cells from the human monocytic cell line THP-1. The original THP-1 cells had been cultured for more than 9 years using 25 cm2 flasks, when cells with a different morphology appeared, adhering to the bottoms of the culture flasks. These were selected by discarding floating nonadherent cells at every subculture. Enrichment of adherent THP-1 cells with long processes proceeded during the cultivation. These adherent THP-1 showed remarkable phenotypic changes, not only morphologically, but also functionally. Namely, increased phagocytic activity, HLA-DR expression and MLR stimulator activity were remarkable. This adherent cell line was designated as activated-THP-1 (A-THP-1), since it demonstrated characteristics of activated macrophages continuously without exogenous stimulation. A cloned A-THP-1 cell line (A-THP-1 C1) also showed the same features and contained about 10% multinucleated giant cells probably caused by cell fusion. This A-THP-1 cell line, the first activated macrophage cell line to be established, provides a good model for understanding of activation mechanisms of macrophages and multinucleation. In this paper, morphological, immunological, and biological characters of this cell line are described.

MeSH terms

  • Actins / analysis
  • Aneuploidy
  • Carboxylesterase
  • Carboxylic Ester Hydrolases / analysis
  • Cell Adhesion
  • Cell Differentiation
  • Cell Line*
  • Chromosomes, Human / ultrastructure
  • Cytokines / pharmacology
  • HLA-DR Antigens / analysis
  • Humans
  • Isoenzymes / analysis
  • Karyotyping
  • L-Lactate Dehydrogenase / analysis
  • Leukemia, Monocytic, Acute / pathology
  • Lymphocyte Culture Test, Mixed
  • Macrophage Activation*
  • Macrophages / cytology*
  • Macrophages / drug effects
  • Macrophages / enzymology
  • Macrophages / ultrastructure
  • Monocytes / cytology
  • Phagocytosis
  • Phenotype
  • Receptors, Complement / analysis
  • Receptors, IgG / analysis
  • Rosette Formation
  • S100 Proteins / analysis
  • Tumor Cells, Cultured / cytology

Substances

  • Actins
  • Cytokines
  • HLA-DR Antigens
  • Isoenzymes
  • Receptors, Complement
  • Receptors, IgG
  • S100 Proteins
  • L-Lactate Dehydrogenase
  • Carboxylic Ester Hydrolases
  • Carboxylesterase