Transcriptional maintenance of cortical somatostatin interneuron subtype identity during migration
Neuron, ISSN: 0896-6273, Vol: 111, Issue: 22, Page: 3590-3603.e5
2023
- 4Citations
- 50Captures
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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
- CrossRef2
- Captures50
- Readers50
- 50
Article Description
Although cardinal cortical interneuron identity is established upon cell-cycle exit, it remains unclear whether specific interneuron subtypes are pre-established, and if so, how their identity is maintained prior to circuit integration. We conditionally removed Sox6 (Sox6-cKO) in migrating somatostatin (Sst + ) interneurons and assessed the effects on their mature identity. In adolescent mice, five of eight molecular Sst + subtypes were nearly absent in the Sox6-cKO cortex without a reduction in cell number. Sox6-cKO cells displayed electrophysiological maturity and expressed genes enriched within the broad class of Sst + interneurons. Furthermore, we could infer subtype identity prior to cortical integration (embryonic day 18.5), suggesting that the loss in subtype was due to disrupted subtype maintenance. Conversely, Sox6 removal at postnatal day 7 did not disrupt marker expression in the mature cortex. Therefore, Sox6 is necessary during migration for maintenance of Sst + subtype identity, indicating that subtype maintenance requires active transcriptional programs.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S0896627323005809; http://dx.doi.org/10.1016/j.neuron.2023.07.018; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85170092559&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/37625400; https://linkinghub.elsevier.com/retrieve/pii/S0896627323005809; https://dx.doi.org/10.1016/j.neuron.2023.07.018
Elsevier BV
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