Protein Kinase C δ: a Gatekeeper of Immune Homeostasis.
Elisabeth SalzerElisangela Santos-ValenteBärbel KellerKlaus WarnatzKaan BoztugPublished in: Journal of clinical immunology (2016)
Human autoimmune disorders present in various forms and are associated with a life-long burden of high morbidity and mortality. Many different circumstances lead to the loss of immune tolerance and often the origin is suspected to be multifactorial. Recently, patients with autosomal recessive mutations in PRKCD encoding protein kinase c delta (PKCδ) have been identified, representing a monogenic prototype for one of the most prominent forms of humoral systemic autoimmune diseases, systemic lupus erythematosus (SLE). PKCδ is a signaling kinase with multiple downstream target proteins and with functions in various signaling pathways. Interestingly, mouse models have indicated a special role of the ubiquitously expressed protein in the control of B-cell tolerance revealed by the severe autoimmunity in Prkcd (-/-) knockout mice as the major phenotype. As such, the study of PKCδ deficiency in humans has tremendous potential in enhancing our knowledge on the mechanisms of B-cell tolerance.
Keyphrases
- protein kinase
- systemic lupus erythematosus
- disease activity
- endothelial cells
- immune response
- mouse model
- healthcare
- signaling pathway
- multiple sclerosis
- drug induced
- pulmonary embolism
- intellectual disability
- early onset
- amino acid
- risk factors
- pluripotent stem cells
- risk assessment
- human health
- cell proliferation
- climate change
- celiac disease