Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Pivot Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Target Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Query: UMLS:C0034186 (
pyelonephritis
)
6,144
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
As central regulators of the adaptive immune response, dendritic cells (DCs) are found in virtually all lymphatic and non-lymphatic organs. A compact network of DCs also spans the kidneys. DCs play a central role in maintenance of organ homeostasis as well as in induction of immune responses against invading pathogens. They can mediate protective or destructive functions in a context-dependent manner.We recently identified CX(3)
CR1
as a kidney-specific "homing receptor" for DCs. There was a strong reduction of DCs in the kidneys of CX(3)
CR1
-deficient mice compared to controls. This reduction was not observed in other organs except the small intestine. As a possible underlying reason we found a strong expression of the CX(3)
CR1
ligand fractalkine in the kidneys. Due to this CX(3)
CR1
-dependent reduction of DCs, especially in the renal cortex, a glomerulonephritis (GN) model was ameliorated in CX(3)
CR1
-deficient mice. In contrast, the immune defense against the most common renal infection, bacterial
pyelonephritis
(PN), was not significantly influenced by CX(3)
CR1
-deficiency. This was explained by the much smaller CX(3)
CR1
-dependency of medullary DCs, which recruit effector cells into the kidney during PN. Additionally, once neutrophils had been recruited by mechanisms distinct from CX(3)
CR1
, they carried out some of the functions of DCs.Taken together, we suggest CX(3)
CR1
as a therapeutic target for GN treatment, as the absence of CX(3)
CR1
selectively influences DCs in the kidney without rendering mice more susceptible towards bacterial kidney infections.
...
PMID:Selective Dependence of Kidney Dendritic Cells on CX3CR1--Implications for Glomerulonephritis Therapy. 2632 46