CDB25:0004094 PILRA — CD8A

Experimentally validated in Human; Orthology-inferred in Rat, Macaque, Pig, Dog, Cow, Chimp, Horse, Marmoset

Title

Journal:; Year Published:

Abstract

The CD8α-PILRα interaction maintains CD8+ T cell quiescence.

Science, 2022; PubMed, Homo sapiens PILRA — Homo sapiens CD8A
ABSTRACT: T cell quiescence is essential for maintaining a broad repertoire against a large pool of diverse antigens from microbes and tumors, but the underlying molecular mechanisms remain largely unknown. We show here that CD8α is critical for the maintenance of CD8+ T cells in a physiologically quiescent state in peripheral lymphoid organs. Upon inducible deletion of CD8α, both naïve and memory CD8+ T cells spontaneously acquired activation phenotypes and subsequently died without exposure to specific antigens. PILRα was identified as a ligand for CD8α in both mice and humans, and disruption of this interaction was able to break CD8+ T cell quiescence. Thus, peripheral T cell pool size is actively maintained by the CD8α-PILRα interaction in the absence of antigen exposure.
Basic Information on PILRA
Ligand Name: paired immunoglobin like type 2 receptor alpha
Other Symbols: FDF03
Ligand Location: secreted based on uniprot, cell membrane based on perplexity, uniprot
HGNC Gene Symbol Report: PILRA
GeneCards: PILRA
Interactions with other Receptors for PILRA
Basic Information on CD8A
Receptor Name: CD8 subunit alpha
Other Symbols: CD8, p32, CD8alpha
Receptor Location: cell membrane based on hpa, perplexity, uniprot
HGNC Gene Symbol Report: CD8A
GeneCards: CD8A
Interactions with other Ligands for CD8A