Neuron cilia restrain glial KCC-3 to a microdomain to regulate multisensory processing
Cell Reports, ISSN: 2211-1247, Vol: 43, Issue: 3, Page: 113844
2024
- 4Citations
- 9Captures
- 8Mentions
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Metrics Details
- Citations4
- Citation Indexes4
- CrossRef4
- Captures9
- Readers9
- Mentions8
- News Mentions8
- 8
Most Recent News
Glial Cells Are More Than Our Brain’s “Glue”
When it comes to brain cells, neurons get the most attention. Their central role in our thoughts, sensations and behaviors has captivated scientists. But neurons
Article Description
Glia interact with multiple neurons, but it is unclear whether their interactions with each neuron are different. Our interrogation at single-cell resolution reveals that a single glial cell exhibits specificity in its interactions with different contacting neurons. Briefly, C. elegans amphid sheath (AMsh) glia apical-like domains contact 12 neuron-endings. At these ad-neuronal membranes, AMsh glia localize the K/Cl transporter KCC-3 to a microdomain exclusively around the thermosensory AFD neuron to regulate its properties. Glial KCC-3 is transported to ad-neuronal regions, where distal cilia of non-AFD glia-associated chemosensory neurons constrain it to a microdomain at AFD-contacting glial membranes. Aberrant KCC-3 localization impacts both thermosensory (AFD) and chemosensory (non-AFD) neuron properties. Thus, neurons can interact non-synaptically through a shared glial cell by regulating microdomain localization of its cues. As AMsh and glia across species compartmentalize multiple cues like KCC-3, we posit that this may be a broadly conserved glial mechanism that modulates information processing across multimodal circuits.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S2211124724001724; http://dx.doi.org/10.1016/j.celrep.2024.113844; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85186741547&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/38421867; https://linkinghub.elsevier.com/retrieve/pii/S2211124724001724; https://dx.doi.org/10.1016/j.celrep.2024.113844
Elsevier BV
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