Flow cytometric detection of cell-associated cytokines in alveolar macrophages

H. Nakamura, S. Fujishima, K. Soejima, Y. Waki, M. Nakamura, A. Ishizaka, M. Kanazawa

Research output: Contribution to journalArticle

9 Citations (Scopus)

Abstract

To elucidate the cytokine-producing capacity of alveolar macrophages (AMs), we have introduced a method of flow cytometry combined with saponin treatment to detect the cell-associated cytokines. We studied bronchoalveolar lavage fluid cells from six patients with sarcoidosis (SAR) and six control (CTL) subjects. Cells were either left uncultured, or cultured with and without lipopolysaccharide (LPS), then treated with paraformaldehyde and saponin and analysed for cell-associated interleukin-1β (IL-1β) and tumour necrosis factor-α (TNF-α) by flow cytometry. Cell-associated IL-1β and TNF-α were also analysed by immunoassays. The flow cytometric cytokine values were correlated with the immunoreactive cell-associated cytokines (IL- 1β: r=0.45, p<0.05; TNF-α: r=0.82, p<0.001). The histograms of cell- associated IL-1β yielded a single peak both in the patients and controls, whereas the histograms of cell-associated TNF-α exhibited two peaks in SAR patients, but just a single peak in the CTL subjects. The mean value of the cell-associated TNF-α in LPS(+) AMs was higher in the SAR patients than in the CTL subjects (p<0.001). In conclusion, the flow cytometric method can be applied to the semiquantitative detection of cell-associated cytokines in alveolar macrophages at the single cell level.

Original languageEnglish
Pages (from-to)1181-1187
Number of pages7
JournalEuropean Respiratory Journal
Volume9
Issue number6
DOIs
Publication statusPublished - 1996 Jul 26

Keywords

  • Alveolar macrophage
  • cell-associated cytokine
  • flow cytometry
  • saponin

ASJC Scopus subject areas

  • Pulmonary and Respiratory Medicine

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