The DOI matches its Crossref record; 4 of the 4 references it cites were found in a registry or an index.
Dissecting the role of PtdIns(4,5)P 2 in endocytosis and recycling of the transferrin receptor
Abstract
Endocytosis and recycling of membrane proteins are key processes for nutrient uptake, receptor signaling and synaptic transmission. Different steps in these fission and fusion cycles have been proposed to be regulated by physiological changes in plasma membrane (PM) phosphatidylinositol (4,5)-bisphosphate [PtdIns(4,5)P2] concentration. Here, we use a chemical enzyme-translocation strategy to rapidly reduce PM PtdIns(4,5)P2 levels while monitoring clathrin-mediated endocytosis and recycling. PtdIns(4,5)P2 hydrolysis blocked transferrin receptor endocytosis and led to a marked increase in the concentration of transferrin receptors in the PM, suggesting that endocytosis is more sensitive to changes in PtdIns(4,5)P2 than recycling. Reduction of PM PtdIns(4,5)P2 levels led to a near complete dissociation of Adaptor protein 2 (AP-2) from the PM but had only a small effect on clathrin assembly. This argues that receptor-mediated PtdIns(4,5)P2 reduction preferentially suppresses AP-2-mediated targeting of cargo to endocytic sites rather than the assembly of clathrin coats or recycling of endocytic vesicles.
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“It has been well established that PIP2, the predominant PI formed at the plasma membrane, is required for clathrin-mediated endocytosis, with roles in clathrin-coated pit initiation, stabilization, and maturation14-17.”
From Transmembrane Protein 55B Is a Novel Regulator of Cellular Cholesterol Metabolism (2014) · cites this paper as [17]
Citations
Cites
Phosphoinositides in cell regulation and membrane dynamics
Di Paolo, G., & De Camilli, P. (2006) · Nature · doi:10.1038/nature05185 · Cited by 2,790
Rapid Chemically Induced Changes of PtdIns(4,5)P 2 Gate KCNQ Ion Channels
Suh, B.-C., Inoue, T., Meyer, T., & Hille, B. (2006) · Science · doi:10.1126/science.1131163 · Cited by 505
Self-citationAn inducible translocation strategy to rapidly activate and inhibit small GTPase signaling pathways.
Inoue, T., Heo, W. D., Grimley, J. S., Wandless, T. J., & Meyer, T. (2005) · Nature Methods · doi:10.1038/nmeth763 · Cited by 424 · cited 1×
“The addition of iRap, a rapamycin analog (Inoue et al., 2005), causes dimerization of a PM-localized FKBP12-rapamycin binding domain (FRB) and a cytosolic Inp54p phosphatase domain conjugated to CFP and FKBP (CF-Inp) (Suh et al., 2006).”
Self-citationPhosphoinositide regulation of clathrin-mediated endocytosis
Haucke, V. (2005) · Biochemical Society Transactions · doi:10.1042/bst0331285 · Cited by 140
Research works printed but not linked: 23
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Cited by
Doherty, G. J., & McMahon, H. T. (2009) · Annual Review of Biochemistry · doi:10.1146/annurev.biochem.78.081307.110540 · Cited by 3,075
Phosphoinositides: Tiny Lipids With Giant Impact on Cell Regulation
Balla, T. (2013) · Physiological Reviews · doi:10.1152/physrev.00028.2012 · Cited by 1,638
The intracellular trafficking pathway of transferrin
Mayle, K. M., Le, A. M., & Kamei, D. T. (2012) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2011.09.009 · Cited by 466
Transmembrane Protein 55B Is a Novel Regulator of Cellular Cholesterol Metabolism
Medina, M. W., Bauzon, F., Naidoo, D., Theusch, E., Stevens, K., Schilde, J., Schubert, C., Mangravite, L. M., Rudel, L. L., Temel, R. E., et al. (2014) · Arteriosclerosis, Thrombosis and Vascular Biology · doi:10.1161/atvbaha.113.302806 · Cited by 24
Metadata
- Authors
- Abe, N., Inoue, T., Galvez, T., Klein, L., & Meyer, T.
- Affiliations
- Graduate Program in Neurosciences, Stanford University School of Medicine, Stanford, CA 94305, USA
- Department of Chemical and Systems Biology, Stanford University School of Medicine, Clark Center, 318 Campus Drive, Stanford, CA 94305, USA
- Graduate Program in Biophysics, and Department of Microbiology and Immunology, Beckman Center, 279 Campus Drive, Stanford University Medical School, Stanford, CA 94305, USA
- Venue
- Journal of Cell Science
- Publisher
- The Company of Biologists
- Published
- 2008-05-01
- Volume
- 121
- Issue
- 9
- Pages
- 1488-1494
- ISSN
- 1477-9137
- 0021-9533
- Cited by
- 77
- References
- 4
- Language
- en
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