Effect of TNF-alpha on Raji cells at different cellular levels estimated by various methods

Ann Hematol. 2006 Feb;85(2):86-94. doi: 10.1007/s00277-005-0010-3. Epub 2005 Nov 1.

Abstract

Tumor necrosis factor (TNF)-alpha, a pleiotropic cytokine, has been shown to induce diverse and opposite effects on lymphoid malignancy depending on TNF receptor system expression. Based on this, we investigated its in vitro dose- and time-related effect on the malignant B-cell line Raji, derived from Burkitt lymphoma patients, at different intracellular levels. The membrane alteration was estimated by lactate dehydrogenase (LDH) release and by flow cytometry; intracellular metabolic energy by determination of the total intracellular LDH activity; total cytosole protein mass by sulforhodamine B assay; and cell growth by incorporation of [3H]thymidine into DNA. Significant increase of LDH through cell membrane alteration was accompanied by decrease of intracellular metabolized energy and total protein mass. TNF-alpha at lower concentrations (125 and 250 pg/ml) significantly induced cell proliferation in comparison with 1,000 pg/ml of TNF-alpha, which induced more cell death. TNF-alpha induced maximal apoptosis rate up to 30% after 24 h, showing more effects for a necrotic form of cell death. Here we reported opposite and diverse effects of TNF-alpha at different intracellular levels in Raji cells, when applied in different assays, showing characteristics for every cellular compartment.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Apoptosis
  • Aspartate Aminotransferases / metabolism
  • Burkitt Lymphoma / drug therapy*
  • Cell Membrane / metabolism
  • Cell Proliferation
  • Creatine Kinase / metabolism
  • Cytological Techniques
  • DNA / metabolism
  • Dose-Response Relationship, Drug
  • Flow Cytometry
  • Humans
  • L-Lactate Dehydrogenase / metabolism
  • Necrosis
  • Rhodamines / metabolism
  • Tumor Necrosis Factor-alpha / therapeutic use*

Substances

  • Rhodamines
  • Tumor Necrosis Factor-alpha
  • lissamine rhodamine B
  • DNA
  • L-Lactate Dehydrogenase
  • Aspartate Aminotransferases
  • Creatine Kinase