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A novel polymorphism of the human CD40 receptor with enhanced function.
- Source :
-
Blood [Blood] 2008 Sep 01; Vol. 112 (5), pp. 1863-71. Date of Electronic Publication: 2008 Jun 30. - Publication Year :
- 2008
-
Abstract
- CD40 signaling is critical for innate and adaptive immunity against pathogens, and the cytoplasmic domain of CD40 is highly conserved both within and between species. A novel missense single nucleotide polymorphism (SNP) in the cytoplasmic domain of CD40 at position 227 (P227A) was identified, which resides on a conserved ancestral haplotype highly enriched in persons of Mexican and South American descent. Functional studies indicated that signaling via human (h) CD40-P227A stably expressed in several B-cell lines led to increased phosphorylation of c-Jun, increased secretion of the pro-inflammatory cytokines interleukin (IL)-6 and TNF-alpha, and increased Ig production, compared with wild-type hCD40. Cooperation between hCD40-P227A signaling and B-cell receptor (BCR)- or Toll-like receptor 9 (TLR9)-mediated signaling was also enhanced, resulting in elevated and synergistic production of IL-6 and Ig. We have thus identified a novel genetic variant of hCD40 with a gain-of-function immune phenotype.
- Subjects :
- Amino Acid Substitution
Animals
B-Lymphocytes immunology
B-Lymphocytes metabolism
CD40 Antigens chemistry
Cell Line
Gene Frequency
Humans
Immunoglobulin M biosynthesis
Interleukin-6 biosynthesis
JNK Mitogen-Activated Protein Kinases metabolism
Mice
Phenotype
Protein Structure, Tertiary
Recombinant Proteins chemistry
Recombinant Proteins genetics
Recombinant Proteins metabolism
Signal Transduction
Toll-Like Receptor 9 metabolism
Transfection
Tumor Necrosis Factor Receptor-Associated Peptides and Proteins metabolism
Tumor Necrosis Factor-alpha metabolism
CD40 Antigens genetics
CD40 Antigens physiology
Polymorphism, Single Nucleotide
Subjects
Details
- Language :
- English
- ISSN :
- 1528-0020
- Volume :
- 112
- Issue :
- 5
- Database :
- MEDLINE
- Journal :
- Blood
- Publication Type :
- Academic Journal
- Accession number :
- 18591382
- Full Text :
- https://doi.org/10.1182/blood-2008-02-138925