Phagocytosis and the actin cytoskeleton.
By R. May, L. Machesky. Journal of Cell Science, 2001
754 citations recorded by the source corpus.
View Paper: https://www.semanticscholar.org/paper/2744010857bffaf28b0c2e534a9a8ecb8da499cb
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- María Yáñez-Mó
- Y. Katare
- K. Wong
- F. Sánchez‐Madrid
- W. Yeap
- O. Barreiro
- J. J. Tai
- S. Wong
Citations in the corpus
- Gene expression profiling reveals the defining features of the classical, intermediate, and nonclassical human monocyte subsets. (2011, background): “These FcR complexes activate WASP2, VASP, PLCG2 and CORO2A leading to cytoskeleton remodeling necessary for phagocytosis.(27) Several complement component genes, including C1QA, C1QB, C2 and C3 were also most highly expressed by the nonclassical subset.”
- Cellular Internalization of Exosomes Occurs Through Phagocytosis (2010, background): “As actin polymerization is required for phagosome formation (36), we next examined the role of the actin cytoskeleton in exosome uptake by RAW 264.”
- Multi-electrode array technologies for neuroscience and cardiology. (2013, background): “This is one of a group of well-known molecular recognition motifs that trigger adhesion and engulfment mechanisms 68 .”
- Particle shape: a new design parameter for micro- and nanoscale drug delivery carriers. (2007, background): “Regardless of the method of administration, particles larger than 500 nm can be phagocytosed by macrophages and smaller particles can be endocytosed by phagocytic or non-phagocytic cells [24, 25].”
- Dynamic interaction of VCAM-1 and ICAM-1 with moesin and ezrin in a novel endothelial docking structure for adherent leukocytes (2002, background): “In this regard, it has been proposed that focal adhesions and complement receptor-mediated phagosomes could share some conserved mechanisms requiring the same molecules (May and Machesky, 2001).”