Germline deletion of CIN85 in humans with X chromosome-linked antibody deficiency.
Baerbel KellerMoneef ShoukierKathrin SchulzArshiya BhattInes HeineValentina StrohmeierCarsten SpeckmannNiklas EngelsKlaus WarnatzJürgen WienandsPublished in: The Journal of experimental medicine (2018)
Ubiquitously expressed Cbl-interacting protein of 85 kD (CIN85) is a multifunctional adapter molecule supposed to regulate numerous cellular processes that are critical for housekeeping as well as cell type-specific functions. However, limited information exists about the in vivo roles of CIN85, because only conditional mouse mutants with cell type-specific ablation of distinct CIN85 isoforms in brain and B lymphocytes have been generated so far. No information is available about the roles of CIN85 in humans. Here, we report on primary antibody deficiency in patients harboring a germline deletion within the CIN85 gene on the X chromosome. In the absence of CIN85, all immune cell compartments developed normally, but B lymphocytes showed intrinsic defects in distinct effector pathways of the B cell antigen receptor, most notably NF-κB activation and up-regulation of CD86 expression on the cell surface. These results reveal nonredundant functions of CIN85 for humoral immune responses.
Keyphrases
- immune response
- end stage renal disease
- copy number
- cell surface
- poor prognosis
- dendritic cells
- oxidative stress
- genome wide
- drug delivery
- healthcare
- chronic kidney disease
- peripheral blood
- binding protein
- peritoneal dialysis
- dna damage
- signaling pathway
- cancer therapy
- dna methylation
- cell proliferation
- lps induced
- replacement therapy
- long non coding rna
- blood brain barrier
- prognostic factors
- amino acid
- pi k akt
- nuclear factor
- patient reported
- subarachnoid hemorrhage
- resting state