Control of chemokine-guided cell migration by ligand sequestration.
By Bijan Boldajipour, Harsha Mahabaleshwar, E. Kardash, M. Reichman-Fried, Heiko Blaser, S. Minina, Duncan Wilson, Qiling Xu, E. Raz. Cell, 2008
635 citations recorded by the source corpus.
Subfields: Immunology, Immunology and Allergy, Oncology
View Paper: https://www.semanticscholar.org/paper/912d0fe0f4b60bfb25009674cae519448b09ddb3
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Citations in the corpus
- Oogenesis in teleosts: how eggs are formed. (2010, background): “sequesters SDF1a, highlighting the importance of ligand clearing during guided cell migration (Boldajipour et al., 2008).”
- Collective cell migration in morphogenesis, regeneration and cancer (2009, background): “Although the precise function of Cxcr7 is unclear, studies from other systems suggest that it might be an 'Sdf1 sink' that sequesters Sdf1 and thereby suppresses Cxcr4 activity in trailing region”
- The Chemokine Superfamily Revisited (2012, neutral): “During embryogenesis, CXCR7 is necessary for proper migration of primordial germ cells to CXCL12 via CXCR4 by acting as a sink for CXCL12 (Boldajipour et al., 2008).”
- International Union of Basic and Clinical Pharmacology. LXXXIX. Update on the Extended Family of Chemokine Receptors and Introducing a New Nomenclature for Atypical Chemokine Receptors (2014, neutral): “Primordial germ cells arrive at sites where Cxcl12 is translated from mRNA but do not continue to migrate forward if the scavenger activity of Ackr3 does not create a guidance cue (Boldajipour et al., 2008).”