1. IL-36γ is secreted through an unconventional pathway using the Gasdermin D and P2X7R membrane pores
- Author
-
Laura D. Manzanares-Meza, Claudia I. Gutiérrez-Román, Albertana Jiménez-Pineda, Felipe Castro-Martínez, Genaro Patiño-López, Eunice Rodríguez-Arellano, Ricardo Valle-Rios, Vianney F. Ortíz-Navarrete, and Oscar Medina-Contreras
- Subjects
IL-36γ ,inflammation ,macrophages ,cytokin receptors ,secretion ,Immunologic diseases. Allergy ,RC581-607 - Abstract
Mucosal innate immunity functions as the first line of defense against invading pathogens. Members of the IL-1 family are key cytokines upregulated in the inflamed mucosa. Inflammatory cytokines are regulated by limiting their function and availability through their activation and secretion mechanisms. IL-1 cytokines secretion is affected by the lack of a signal peptide on their sequence, which prevents them from accessing the conventional protein secretion pathway; thus, they use unconventional protein secretion pathways. Here we show in mouse macrophages that LPS/ATP stimulation induces cytokine relocalization to the plasma membrane, and conventional secretion blockade using monensin or Brefeldin A triggers no IL-36γ accumulation within the cell. In silico modeling indicates IL-36γ can pass through both the P2X7R and Gasdermin D pores, and both IL-36γ, P2X7R and Gasdermin D mRNA are upregulated in inflammation; further, experimental blockade of these receptors’ limits IL-36γ release. Our results demonstrate that IL-36γ is secreted mainly by an unconventional pathway through membrane pores formed by P2X7R and Gasdermin D.
- Published
- 2022
- Full Text
- View/download PDF