Intracellular Routes and Selective Retention of Antigens in Mildly Acidic Cathepsin D/Lysosome-Associated Membrane Protein-1/MHC Class II-Positive Vesicles in Immature Dendritic Cells

Manfred B. Lutz, Patrizia Rovere, Monique J. Kleijmeer, Maria Rescigno, Caroline U. Aßmann, Viola M J Oorschot, Hans J. Geuze, Jeannine Trucy, Denis Demandolx, Jean Davoust, Paola Ricciardi-Castagnoli

Research output: Contribution to journalArticlepeer-review

Abstract

Immature dendritic cells (DC) use both macropinocytosis and mannose receptor-mediated endocytosis to internalize soluble Ags efficiently. These Ags are ultimately presented to T cells after DC maturation and migration into the lymph nodes. We have previously described the immortalized myeloid cell line FSDC as displaying the characteristics of early DC precursors that efficiently internalize soluble Ags. To describe the different routes of Ag uptake and to identify the Ag retention compartments in FSDC, we followed the intracellular fate of FITC-coupled OVA, dextran (DX), transferrin, and Lucifer Yellow using flow cytometry, confocal microscopy, and immunoelectron microscopy. OVA and DX gained access into macropinosomes and early endosomes. DX was preferentially sorted into endosomal compartments, while most of the OVA entered macropinosomes via fluid phase uptake. We found a long-lasting retention of DX and OVA of up to 24 h. After 6 h of chase, these two molecules were concentrated in common vesicular compartments. These retention compartments were distinct from endosomes and lysosomes; they were much larger, only mildly acidic, and lacked the small GTP binding protein rab7. However, they were positive for lysosome-associated membrane protein-1, the protease cathepsin D, and MHC class II molecules, thus representing matured macropinosomes. These data suggest that the activity of vacuolar proteases is reduced at the mildly acidic pH of these vesicles, which explains their specific retention of an Ag. The retention compartments might be used by nonlymphoid tissue DC to store peripheral Ags during their migration to the lymph node.

Original languageEnglish
Pages (from-to)3707-3716
Number of pages10
JournalJournal of Immunology
Volume159
Issue number8
Publication statusPublished - Oct 15 1997

ASJC Scopus subject areas

  • Immunology

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