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Batf3-dependent dendritic cells in the renal lymph node induce tolerance against circulating antigens.


ABSTRACT: Although the spleen is a major site where immune tolerance to circulating innocuous antigens occurs, the kidney also contributes. Circulating antigens smaller than albumin are constitutively filtered and concentrated in the kidney and reach the renal lymph node by lymphatic drainage, where resident dendritic cells (DCs) capture them and induce tolerance of specific cytotoxic T cells through unknown mechanisms. Here, we found that the coinhibitory cell surface receptor programmed death 1 (PD-1) on cytotoxic T cells mediates to their tolerance. Renal lymph node DCs of the CD8(+) XCR1(+) subset, which depend on the transcription factor Batf3, expressed the PD-1 cognate ligand PD-L1. Batf3-dependent DCs in the renal lymph node presented antigen that had been concentrated in the kidney and used PD-L1 to induce apoptosis of cytotoxic T cells. In contrast, T cell tolerance in the spleen was independent of PD-1, PD-L1, and Batf3. In summary, these results clarify how the kidney/renal lymph node system tolerizes the immune system against circulating innocuous antigens.

SUBMITTER: Gottschalk C 

PROVIDER: S-EPMC3609142 | biostudies-literature | 2013 Mar

REPOSITORIES: biostudies-literature

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Batf3-dependent dendritic cells in the renal lymph node induce tolerance against circulating antigens.

Gottschalk Catherine C   Damuzzo Vera V   Gotot Janine J   Kroczek Richard A RA   Yagita Hideo H   Murphy Kenneth M KM   Knolle Percy A PA   Ludwig-Portugall Isis I   Kurts Christian C  

Journal of the American Society of Nephrology : JASN 20130214 4


Although the spleen is a major site where immune tolerance to circulating innocuous antigens occurs, the kidney also contributes. Circulating antigens smaller than albumin are constitutively filtered and concentrated in the kidney and reach the renal lymph node by lymphatic drainage, where resident dendritic cells (DCs) capture them and induce tolerance of specific cytotoxic T cells through unknown mechanisms. Here, we found that the coinhibitory cell surface receptor programmed death 1 (PD-1) o  ...[more]

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