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Analysis of the survival of mature human eosinophils: interleukin-5 prevents apoptosis in mature human eosinophils

Blood. 1991 Nov 15;78(10):2542-7.

Abstract

We and other groups have previously shown that interleukin-5 (IL-5) maintained the viability of mature eosinophils in an in vitro liquid culture system. Mature eosinophils did not proliferate but their survival was maintained in the presence of IL-5. Using this culture system, we investigated the mechanism of IL-5-mediated survival. In the absence of human IL-5 (hIL-5) mature eosinophils succumbed after 4 days, while in the presence of hIL-5 they survived up to 10 days. When DNA extracts of cultured eosinophils were analyzed on an agar gel electrophoresis, marked DNA fragmentation was observed in the absence of hIL-5, while no significant DNA fragmentation was observed in the culture with hIL-5 for 48 hours. The DNA fragmentation appeared as early as 6 to 12 hours after hIL-5 deprivation. Concomitantly, IL-5 stimulated total RNA and protein synthesis, but did not induce DNA synthesis in mature eosinophils. Because cycloheximide or actinomycin D impeded the protection of apoptosis by hIL-5, some new RNA and protein synthesis appeared to be required in this phenomena. These findings indicate that IL-5 maintains survival of mature eosinophils with induction of new RNA and protein synthesis, thus leading to the inhibition of apoptosis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Death / drug effects*
  • Cell Survival / drug effects*
  • Cells, Cultured
  • Cycloheximide / pharmacology
  • Cytokines / pharmacology*
  • DNA / biosynthesis
  • DNA / drug effects
  • DNA / isolation & purification
  • Dactinomycin / pharmacology
  • Eosinophils / cytology*
  • Eosinophils / drug effects
  • Eosinophils / physiology
  • Granulocyte Colony-Stimulating Factor / pharmacology
  • Granulocyte-Macrophage Colony-Stimulating Factor / pharmacology
  • Humans
  • Interleukin-2 / pharmacology
  • Interleukin-3 / pharmacology
  • Interleukin-5 / pharmacology*
  • Kinetics
  • RNA / biosynthesis
  • Recombinant Proteins / pharmacology

Substances

  • Cytokines
  • Interleukin-2
  • Interleukin-3
  • Interleukin-5
  • Recombinant Proteins
  • Granulocyte Colony-Stimulating Factor
  • Dactinomycin
  • RNA
  • Granulocyte-Macrophage Colony-Stimulating Factor
  • DNA
  • Cycloheximide