Two Discrete Types of Tumor Necrosis Factor-resistant Cells Derived from the Same Cell Line

Bart Vanhaesebroeck, Sigrid Van Bladel, Anne Lenaerts, Philip Suffys, Rudi Beyaert, Rudolf Lucas, Frans Van Roy, Walter Fiers

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Abstract

From the murine fibrosarcoma cell line L929s, which is sensitive to tumor necrosis factor (TNF)-mediated cell lysis, two discrete types of TNF-resistant variants were derived by TNF selection. Cells of the first type (named L929rl) were not sensitized to TNF cytotoxicity by cotreatment with either inhibitors of protein or RNA synthesis, or -y-interferon, despite the presence of a functional γ-interferon response. L929rl constitutively produced TNF in the supernatant and expressed membranebound TNF, which was not bound to the TNF receptor. In fact, TNF receptors could not be demonstrated on L929rl cells, not even after low pH treatment and/or incubation with antiserum to TNF. L929rl exhibited a stable TNF-resistant phenotype in the absence of further TNF selection. No evidence could be obtained that TNF acted as an autocrine growth factor for these cells. L929r2, the second type of TNF-resistant L929 cells, became sensitive to TNF lysis in the presence of RNA or protein synthesis inhibitors, or in the presence of γ-interferon. TNF induced the secretion of interleukin 6 in these cells, additionally showing that functional TNF signaling in these cells indeed takes place, but does not lead to cell lysis under normal conditions. L929r2 did not produce TNF, also not upon stimulation with exogenous TNF. The number and binding affinity of TNF receptors were not consistently different between L929s and L929r2 cells. In the absence of further TNF selection, L929r2 gradually reverted to TNF sensitivity. This sensitivity was not reversible to TNF resistance by the gene-regulatory agents 5-azacytidine or sodium butyrate. Treatment with these agents also did not affect the TNF sensitivity of L929s cells nor the TNF resistance of L929rl and L929r2 cells. In summary, our results suggest the existence among cells of the same cell line of discrete mechanisms for acquisition of resistance to TNF-mediated cell lysis.

Original languageEnglish (US)
Pages (from-to)2469-2477
Number of pages9
JournalCancer Research
Volume51
Issue number9
StatePublished - Jan 1 1991

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Tumor Necrosis Factor-alpha
Cell Line
Tumor Necrosis Factor Receptors
Interferons
Nucleic Acid Synthesis Inhibitors
Protein Synthesis Inhibitors
Azacitidine
Butyric Acid
Fibrosarcoma
Regulator Genes
Immune Sera

ASJC Scopus subject areas

  • Oncology
  • Cancer Research

Cite this

Vanhaesebroeck, B., Bladel, S. V., Lenaerts, A., Suffys, P., Beyaert, R., Lucas, R., ... Fiers, W. (1991). Two Discrete Types of Tumor Necrosis Factor-resistant Cells Derived from the Same Cell Line. Cancer Research, 51(9), 2469-2477.

Two Discrete Types of Tumor Necrosis Factor-resistant Cells Derived from the Same Cell Line. / Vanhaesebroeck, Bart; Bladel, Sigrid Van; Lenaerts, Anne; Suffys, Philip; Beyaert, Rudi; Lucas, Rudolf; Roy, Frans Van; Fiers, Walter.

In: Cancer Research, Vol. 51, No. 9, 01.01.1991, p. 2469-2477.

Research output: Contribution to journalArticle

Vanhaesebroeck, B, Bladel, SV, Lenaerts, A, Suffys, P, Beyaert, R, Lucas, R, Roy, FV & Fiers, W 1991, 'Two Discrete Types of Tumor Necrosis Factor-resistant Cells Derived from the Same Cell Line', Cancer Research, vol. 51, no. 9, pp. 2469-2477.
Vanhaesebroeck B, Bladel SV, Lenaerts A, Suffys P, Beyaert R, Lucas R et al. Two Discrete Types of Tumor Necrosis Factor-resistant Cells Derived from the Same Cell Line. Cancer Research. 1991 Jan 1;51(9):2469-2477.
Vanhaesebroeck, Bart ; Bladel, Sigrid Van ; Lenaerts, Anne ; Suffys, Philip ; Beyaert, Rudi ; Lucas, Rudolf ; Roy, Frans Van ; Fiers, Walter. / Two Discrete Types of Tumor Necrosis Factor-resistant Cells Derived from the Same Cell Line. In: Cancer Research. 1991 ; Vol. 51, No. 9. pp. 2469-2477.
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abstract = "From the murine fibrosarcoma cell line L929s, which is sensitive to tumor necrosis factor (TNF)-mediated cell lysis, two discrete types of TNF-resistant variants were derived by TNF selection. Cells of the first type (named L929rl) were not sensitized to TNF cytotoxicity by cotreatment with either inhibitors of protein or RNA synthesis, or -y-interferon, despite the presence of a functional γ-interferon response. L929rl constitutively produced TNF in the supernatant and expressed membranebound TNF, which was not bound to the TNF receptor. In fact, TNF receptors could not be demonstrated on L929rl cells, not even after low pH treatment and/or incubation with antiserum to TNF. L929rl exhibited a stable TNF-resistant phenotype in the absence of further TNF selection. No evidence could be obtained that TNF acted as an autocrine growth factor for these cells. L929r2, the second type of TNF-resistant L929 cells, became sensitive to TNF lysis in the presence of RNA or protein synthesis inhibitors, or in the presence of γ-interferon. TNF induced the secretion of interleukin 6 in these cells, additionally showing that functional TNF signaling in these cells indeed takes place, but does not lead to cell lysis under normal conditions. L929r2 did not produce TNF, also not upon stimulation with exogenous TNF. The number and binding affinity of TNF receptors were not consistently different between L929s and L929r2 cells. In the absence of further TNF selection, L929r2 gradually reverted to TNF sensitivity. This sensitivity was not reversible to TNF resistance by the gene-regulatory agents 5-azacytidine or sodium butyrate. Treatment with these agents also did not affect the TNF sensitivity of L929s cells nor the TNF resistance of L929rl and L929r2 cells. In summary, our results suggest the existence among cells of the same cell line of discrete mechanisms for acquisition of resistance to TNF-mediated cell lysis.",
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