| http://purl.uniprot.org/citations/30638932 | http://www.w3.org/1999/02/22-rdf-syntax-ns#type | http://purl.uniprot.org/core/Journal_Citation |
| http://purl.uniprot.org/citations/30638932 | http://www.w3.org/2000/01/rdf-schema#comment | "Dendritic cells (DCs) are professional antigen-presenting cells. The main function of DCs is to process antigen and present it to the T cells to induce T cell immunity. In addition to their function as potent stimulators of adaptive immunity, DCs are also crucial for maintaining immunological tolerance through the induction of peripheral regulatory T cells. Tumor necrosis factor-α-induced protein 8-2 (Tumor necrosis factor-α induced protein-8-like 2, TNFAIP8L2 or TIPE2) was expressed primarily by immune cells and maintains immune tolerance through the negative regulation of innate and adaptive immune responses. Previous studies indicate that TIPE2 in DCs may inhibit the innate immune response to RNA. However, the role of TIPE2 in DCs in the induction of peripheral tolerance remains unknown. Our current study showed that Tipe2-deficient DCs are more immature under homeostatic condition and consequently promote the induction of peripheral Tregs in the gut mucosa. Mechanistic studies revealed that TIPE2 promotes the expression of DC maturation markers CD80 and CD86 through the activation of PI3K-PKCδ-MAPK signaling pathway during the differentiation of DCs. Taken together, these results indicate that, in addition to acting as a negative regulator of pathogen-induced immune response, TIPE2 in DCs is also capable of promoting immune response under homeostatic condition through the suppression of peripheral tolerance."xsd:string |
| http://purl.uniprot.org/citations/30638932 | http://purl.org/dc/terms/identifier | "doi:10.1016/j.bbrc.2019.01.008"xsd:string |
| http://purl.uniprot.org/citations/30638932 | http://purl.uniprot.org/core/author | "Liu C."xsd:string |
| http://purl.uniprot.org/citations/30638932 | http://purl.uniprot.org/core/author | "Liu R."xsd:string |
| http://purl.uniprot.org/citations/30638932 | http://purl.uniprot.org/core/author | "Fan T."xsd:string |
| http://purl.uniprot.org/citations/30638932 | http://purl.uniprot.org/core/author | "Geng W."xsd:string |
| http://purl.uniprot.org/citations/30638932 | http://purl.uniprot.org/core/author | "Liu C.'"xsd:string |
| http://purl.uniprot.org/citations/30638932 | http://purl.uniprot.org/core/author | "Ruan Q."xsd:string |
| http://purl.uniprot.org/citations/30638932 | http://purl.uniprot.org/core/date | "2019"xsd:gYear |
| http://purl.uniprot.org/citations/30638932 | http://purl.uniprot.org/core/name | "Biochem Biophys Res Commun"xsd:string |
| http://purl.uniprot.org/citations/30638932 | http://purl.uniprot.org/core/pages | "911-917"xsd:string |
| http://purl.uniprot.org/citations/30638932 | http://purl.uniprot.org/core/title | "TIPE2 in dendritic cells inhibits the induction of pTregs in the gut mucosa."xsd:string |
| http://purl.uniprot.org/citations/30638932 | http://purl.uniprot.org/core/volume | "509"xsd:string |
| http://purl.uniprot.org/citations/30638932 | http://www.w3.org/2004/02/skos/core#exactMatch | http://purl.uniprot.org/pubmed/30638932 |
| http://purl.uniprot.org/citations/30638932 | http://xmlns.com/foaf/0.1/primaryTopicOf | https://pubmed.ncbi.nlm.nih.gov/30638932 |
| http://purl.uniprot.org/uniprot/#_Q9D8Y7-mappedCitation-30638932 | http://www.w3.org/1999/02/22-rdf-syntax-ns#object | http://purl.uniprot.org/citations/30638932 |
| http://purl.uniprot.org/uniprot/#_Q6P589-mappedCitation-30638932 | http://www.w3.org/1999/02/22-rdf-syntax-ns#object | http://purl.uniprot.org/citations/30638932 |
| http://purl.uniprot.org/uniprot/Q9D8Y7 | http://purl.uniprot.org/core/mappedCitation | http://purl.uniprot.org/citations/30638932 |
| http://purl.uniprot.org/uniprot/Q6P589 | http://purl.uniprot.org/core/mappedCitation | http://purl.uniprot.org/citations/30638932 |