Results 1 to 10 of about 3,455 (202)

Crosstalk between CXCL12/CXCR4/ACKR3 and the STAT3 Pathway [PDF]

open access: yesCells
The reciprocal modulation between the CXCL12/CXCR4/ACKR3 axis and the STAT3 signaling pathway plays a crucial role in the progression of various diseases and neoplasms. Activation of the CXCL12/CXCR4/ACKR3 axis triggers the STAT3 pathway through multiple
Zelong Ma   +3 more
doaj   +5 more sources

Reassessing the adrenomedullin scavenging function of ACKR3 in lymphatic endothelial cells.

open access: yesPLoS ONE, 2023
Atypical chemokine receptor 3 (ACKR3) is a scavenger of the chemokines CXCL11 and CXCL12 and of several opioid peptides. Additional evidence indicates that ACKR3 binds two other non-chemokine ligands, namely the peptide hormone adrenomedullin (AM) and ...
Elena C Sigmund   +7 more
doaj   +7 more sources

ACKR3 regulates platelet activation and ischemia-reperfusion tissue injury

open access: yesNature Communications, 2022
ACKR3 is a critical regulator of platelet-mediated thrombosis and organ injury following ischemia/reperfusion. Platelet ACKR3 surface expression is independently associated with all-cause mortality in patients with cardiovascular diseases.
Anne-Katrin Rohlfing   +42 more
doaj   +5 more sources

ACKR3 promotes CXCL12/CXCR4-mediated cell-to-cell-induced lymphoma migration through LTB4 production [PDF]

open access: yesFrontiers in Immunology, 2023
Chemotaxis is an essential physiological process, often harnessed by tumors for metastasis. CXCR4, its ligand CXCL12 and the atypical receptor ACKR3 are overexpressed in many human cancers.
Paola Antonello   +10 more
doaj   +4 more sources

Heterogeneous expression of the atypical chemokine receptor ACKR3 in glioblastoma patient-derived tissue samples and cell cultures [PDF]

open access: yesScientific Reports
Glioblastoma (GBM) is the most aggressive glial tumor of the adult brain, associated with invariably fatal outcome, and a deeper understanding of the underlying malignant mechanisms is necessary to address the current therapeutic failure.
Damla Isci   +9 more
doaj   +3 more sources

Quantification of increased biologically active CXCL12α plasma concentrations after ACKR3 antagonist treatment in humans [PDF]

open access: yesClinical and Translational Science
CXCL12 acts as a chemoattractant by binding to the receptor CXCR4. The (atypical) chemokine receptor ACKR3 (CXCR7) scavenges CXCL12. Antagonism of ACKR3 thus leads to an increase in CXCL12 concentrations that has been used as a pharmacodynamic biomarker ...
Peter Blattmann   +10 more
doaj   +3 more sources

Constitutive activity of an atypical chemokine receptor revealed by inverse agonistic nanobodies [PDF]

open access: yesNature Communications
Stimulation of atypical chemokine receptor 3 (ACKR3) by chemokines does not activate G proteins but recruits arrestin. It is a chemokine scavenger that indirectly influences responses by restricting the availability of CXCL12, an agonist shared with the ...
Claudia V. Perez Almeria   +19 more
doaj   +3 more sources

D-dopachrome tautomerase contributes to lung epithelial repair via atypical chemokine receptor 3-dependent Akt signaling [PDF]

open access: yesEBioMedicine, 2021
Background: Emphysematous COPD is characterized by aberrant alveolar repair. Macrophage migration inhibitory factor (MIF) contributes to alveolar repair, but for its structural and functional homolog D-dopachrome tautomerase (DDT) this is unknown.
Shanshan Song   +11 more
doaj   +3 more sources

Distinct activation mechanisms of CXCR4 and ACKR3 revealed by single-molecule analysis of their conformational landscapes [PDF]

open access: yeseLife
The canonical chemokine receptor CXCR4 and atypical receptor ACKR3 both respond to CXCL12 but induce different effector responses to regulate cell migration.
Christopher T Schafer   +4 more
doaj   +2 more sources

Structural basis of ligand interaction with atypical chemokine receptor 3 [PDF]

open access: yesNature Communications, 2017
The atypical chemokine receptor 3 (ACKR3) is important for cell migration in development and cancer. Here the authors combine radiolytic footprinting, disulfide trapping, mutagenesis and molecular modelling to characterize the ligand interactions and ...
Martin Gustavsson   +10 more
doaj   +3 more sources

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