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April 1, 1987The Journal of Immunology182 citations

Ligand-receptor interactions required for commitment to the activation of the interleukin 2 gene.

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AWA WeissRSRobert L. ShieldsMNM Newton

Key Points

  • This research aims to investigate the role of ligand-receptor interactions in activating the interleukin 2 gene in T cells.
  • Activated human T cell line Jurkat using Concanavalin A (Con A) and PMA for stimulation.
  • Examined time-dependent requirement of simultaneous stimulation for 2 to 4 hours.
  • Measured secreted interleukin 2 and mRNA levels as indicators of activation.
  • Simultaneous stimulation with Con A and PMA for 2 to 4 hours is required for interleukin 2 production.
  • IL 2 mRNA appearance correlates with the activation timeline and requires ongoing protein synthesis.
  • alpha-methyl mannoside reverses effects of Con A, highlighting importance of ligand-receptor interaction.

Abstract

Concanavalin A (Con A), which together with phorbol myristate acetate (PMA) can activate the human T cell line Jurkat to produce interleukin 2 (IL 2), is shown to depend on the expression of the T3/T cell antigen receptor heterodimer (T3/Ti) complex to induce activation. alpha-methyl mannoside was able to reverse all of the observed effects of Con A on intracellular biochemical events. Therefore, ligand-receptor occupancy appears to be required for sustaining biochemical events associated with triggering the T3/Ti complex. Studies of the time-dependent requirements for the two stimuli required for activation revealed that simultaneous stimulation with both Con A and PMA is required for 2 to 4 hr for the cell to commit itself to activation, as measured by the appearance of secreted IL 2. This 2- to 4-hr requirement correlated precisely with the appearance of IL 2 mRNA, and the appearance of IL 2 transcripts depended on protein synthesis during this critical time period.

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Cite This Study

Weiss et al. (1987) studied this question.

synapsesocial.com/papers/6a22475c1b095894fc4ee84fhttps://doi.org/10.4049/jimmunol.138.7.2169
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