◀ Back to CD47
CD47 — THBS1
Pathways - manually collected, often from reviews:
-
KEGG ECM-receptor interaction:
COMP/THBS1/THBS2/THBS3/THBS4
→
CD47
(protein-protein, activation)
-
NCI Pathway Database Beta3 integrin cell surface interactions:
CD47 (CD47)
→
alphaIIb/beta3 Integrin/CD47/Thrombospondin complex (CD47-ITGA2B-ITGB3-THBS1)
(modification, collaborate)
Fujimoto et al., J Biol Chem 2003*, Plow et al., Blood 1985, Chung et al., J Biol Chem 1997
Evidence: physical interaction
-
NCI Pathway Database Beta3 integrin cell surface interactions:
CD47 (CD47)
→
Thrombospondin complex (THBS1)
(modification, collaborate)
Fujimoto et al., J Biol Chem 2003*, Plow et al., Blood 1985, Chung et al., J Biol Chem 1997
Evidence: physical interaction
-
NCI Pathway Database Beta3 integrin cell surface interactions:
alphaIIb/beta3 Integrin complex (ITGA2B-ITGB3)
→
alphaIIb/beta3 Integrin/CD47/Thrombospondin complex (CD47-ITGA2B-ITGB3-THBS1)
(modification, collaborate)
Fujimoto et al., J Biol Chem 2003*, Plow et al., Blood 1985, Chung et al., J Biol Chem 1997
Evidence: physical interaction
-
NCI Pathway Database Beta3 integrin cell surface interactions:
alphaIIb/beta3 Integrin/CD47/Thrombospondin complex (CD47-ITGA2B-ITGB3-THBS1)
→
Thrombospondin complex (THBS1)
(modification, collaborate)
Fujimoto et al., J Biol Chem 2003*, Plow et al., Blood 1985, Chung et al., J Biol Chem 1997
Evidence: physical interaction
Protein-Protein interactions - manually collected from original source literature:
Studies that report less than 10 interactions are marked with *
Text-mined interactions from Literome
Isenberg et al., J Biol Chem 2006
:
Therefore, ligation of either CD36 or CD47 is sufficient to inhibit NO-stimulated vascular cell responses and cGMP signaling, but only
CD47 is
necessary for this activity of
thrombospondin-1 at physiological concentrations
Sarfati et al., Curr Drug Targets 2008
:
CD47 in the immune response :
role of
thrombospondin and SIRP-alpha reverse signaling
Miller et al., Matrix Biol 2013
:
Therefore, engaging
CD47 is necessary and
sufficient for
thrombospondin-1 to inhibit H2S dependent T cell activation