Regulation of Latent Sensory Hair Cell Precursors by Glia in the Zebrafish Lateral Line
Neuron, ISSN: 0896-6273, Vol: 45, Issue: 1, Page: 69-80
2005
- 109Citations
- 117Captures
Metric Options: Counts1 Year3 YearSelecting the 1-year or 3-year option will change the metrics count to percentiles, illustrating how an article or review compares to other articles or reviews within the selected time period in the same journal. Selecting the 1-year option compares the metrics against other articles/reviews that were also published in the same calendar year. Selecting the 3-year option compares the metrics against other articles/reviews that were also published in the same calendar year plus the two years prior.
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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
- Citations109
- Citation Indexes109
- CrossRef109
- 102
- Captures117
- Readers117
- 117
Article Description
The lateral line is a placodally derived mechanosensory organ in anamniotes that detects the movement of water. In zebrafish embryos, a migrating primordium deposits seven to nine clusters of sensory hair cells, or neuromasts, at intervals along the trunk. Postembryonically, neuromasts continue to be added. We show that some secondary neuromasts arise from a pool of latent precursors that are deposited by the primordium between primary neuromasts. Interneuromast cells lie adjacent to the lateral line nerve and associated glia. These cells remain quiescent while they are juxtaposed with the glia; however, when they move away from the nerve they increase proliferation and form neuromasts. If glia are manually removed or genetically ablated by mutations in cls / sox10, hypersensitive ( hps ), or rowgain ( rog ), neuromasts precociously differentiate. Transplantation of wt glia into mutants rescues the appropriate temporal differentiation of interneuromast cells. Our studies reveal a role for glia in regulating sensory hair cell precursors.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S0896627304008384; http://dx.doi.org/10.1016/j.neuron.2004.12.020; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=11344262287&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/15629703; https://linkinghub.elsevier.com/retrieve/pii/S0896627304008384; https://dx.doi.org/10.1016/j.neuron.2004.12.020
Elsevier BV
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