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:C0038002 (
splenomegaly
)
9,873
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
Phagocytosis of apoptotic cells (efferocytosis) is essential for regulation of immune responses and tissue homeostasis and is mediated by phagocytic receptors. In this study, we found that
urokinase plasminogen activator receptor
(
uPAR
) plays an important role in internalization of apoptotic cells and also characterized the underlying mechanisms. In a flow cytometry-based phagocytic assay,
uPAR
-deficient macrophages displayed significant defect in internalization but not tethering of apoptotic cells. When
uPAR
-deficient mice were challenged with apoptotic cells, they exhibited pronounced
splenomegaly
resulting from accumulation of abundant apoptotic cells in spleen. Overexpression of
uPAR
in HEK-293 cells enhanced efferocytosis, which was inhibited by Annexin V and phosphatidylserine (PS) liposome, suggesting that
uPAR
-mediated efferocytosis is dependent on PS. In serum lacking high m.w. kininogen (HK), a
uPAR
ligand,
uPAR
-mediated efferocytosis was significantly attenuated, which was rescued by replenishment of HK. As detected by flow cytometry, HK selectively bound to apoptotic cells, but not viable cells. In purified systems, HK was specifically associated with PS liposome. HK binding to apoptotic cells induced its rapid cleavage to the two-chain form of HK (HKa) and bradykinin. Both the H chain and L chain of HKa were associated with PS liposome and apoptotic cells. HKa has higher binding affinity than HK to
uPAR
. Overexpression of Rac1/N17 cDNA inhibited
uPAR
-mediated efferocytosis. HK plus PS liposome stimulated a complex formation of CrkII with p130Cas and Dock-180 and Rac1 activation in
uPAR
-293 cells, but not in control HEK-293 cells. Thus,
uPAR
mediates efferocytosis through HK interaction with PS on apoptotic cells and activation of the Rac1 pathway.
...
PMID:High molecular weight kininogen binds phosphatidylserine and opsonizes urokinase plasminogen activator receptor-mediated efferocytosis. 2468 27