Endosomes: A legitimate platform for the signaling train
Open accessAbstract
Although long regarded as a conduit for the degradation or recycling of cell surface receptors, the endosomal system is also an essential site of signal transduction. Activated receptors accumulate in endosomes, and certain signaling components are exclusively localized to endosomes. Receptors can continue to transmit signals from endosomes that are different from those that arise from the plasma membrane, resulting in distinct physiological responses. Endosomal signaling is widespread in metazoans and plants, where it transmits signals for diverse receptor families that regulate essential processes including growth, differentiation and survival. Receptor signaling at endosomal membranes is tightly regulated by mechanisms that control agonist availability, receptor coupling to signaling machinery, and the subcellular localization of signaling components. Drugs that target mechanisms that initiate and terminate receptor signaling at the plasma membrane are widespread and effective treatments for disease. Selective disruption of receptor signaling in endosomes, which can be accomplished by targeting endosomal-specific signaling pathways or by selective delivery of drugs to the endosomal network, may provide novel therapies for disease.
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Signaling receptors can be degraded or recycled to the surface after binding of their ligands and can be active at the surface and/or intracellularly.
“Signaling receptors can be degraded or recycled to the surface after binding of their ligands [74] and can be active at the surface and/or intracellularly.”
From Sorting nexin 17 regulates ApoER2 recycling and reelin signaling (2014) · cites this paper as [74]
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- Authors
- Murphy, J. E., Padilla, B. E., Hasdemir, B., Cottrell, G. S., & Bunnett, N. W.
- Affiliations
- University of California, San Francisco (US)
- University of Bath (GB)
- Venue
- Proceedings of the National Academy of Sciences
- Publisher
- National Academy of Sciences
- Published
- 2009-10-20
- Volume
- 106
- Issue
- 42
- Pages
- 17615-17622
- ISSN
- 0027-8424 (ISSN-L)
- 1091-6490
- PMC
- PMC2764915
- OpenAlex
- W2056442594
- Cited by
- 373
- References
- 0
- Citations by year
- 2026: 7 · 2025: 13 · 2024: 20 · 2023: 24 · 2022: 11 · 2021: 18 · 2020: 13 · 2019: 21 · 2018: 22 · 2017: 17 · 2016: 21 · 2015: 17 · 2014: 37 · 2013: 32 · 2012: 39
- FWCI
- 2.55
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Proceedings of the National Academy of Sciences (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- CentAUR (University of Reading) (submittedVersion)
- Funders
- British Heart Foundation (FS/08/017/25027)
- National Institute of Diabetes and Digestive and Kidney Diseases (DK-39957, R37DK039957, DK 57840, DK 43207, R01DK057840, R01DK043207, R01DK039957, R56DK043207)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Cellular transport and secretion
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Receptor Mechanisms and Signaling
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Physiology › Calcium signaling and nucleotide metabolism
- Keywords
- endosomes, endosomal signaling, receptor signaling, signal transduction, receptor internalization, receptor degradation, receptor recycling, receptor coupling, targeted therapy
- MeSH terms
- Animals, Endocytosis, Humans, Models, Biological, Peptide Hydrolases, Endosomes, Signal Transduction, Receptor Protein-Tyrosine Kinases, MAP Kinase Signaling System, Receptors, G-Protein-Coupled, Toll-Like Receptors, Ubiquitination
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