Receptor for advanced glycation end-products (RAGE) mediates phagocytosis in nonprofessional phagocytes

Commun Biol. 2022 Aug 16;5(1):824. doi: 10.1038/s42003-022-03791-1.

Abstract

In mammals, both professional phagocytes and nonprofessional phagocytes (NPPs) can perform phagocytosis. However, limited targets are phagocytosed by NPPs, and thus, the mechanism remains unclear. We find that spores of the yeast Saccharomyces cerevisiae are internalized efficiently by NPPs. Analyses of this phenomenon reveals that RNA fragments derived from cytosolic RNA species are attached to the spore wall, and these fragments serve as ligands to induce spore internalization. Furthermore, we show that a multiligand receptor, RAGE (receptor for advanced glycation end-products), mediates phagocytosis in NPPs. RAGE-mediated phagocytosis is not uniquely induced by spores but is an intrinsic mechanism by which NPPs internalize macromolecules containing RAGE ligands. In fact, artificial particles labeled with polynucleotides, HMGB1, or histone (but not bovine serum albumin) are internalized in NPPs. Our findings provide insight into the molecular basis of phagocytosis by NPPs, a process by which a variety of macromolecules are targeted for internalization.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Ligands
  • Mammals
  • Phagocytes*
  • Phagocytosis
  • RNA
  • Receptor for Advanced Glycation End Products
  • Receptors, Immunologic*

Substances

  • Ligands
  • Receptor for Advanced Glycation End Products
  • Receptors, Immunologic
  • RNA