4.7 Article

Morphological Diversity of Calretinin Interneurons Generated From Adult Mouse Olfactory Bulb Core Neural Stem Cells

期刊

出版社

FRONTIERS MEDIA SA
DOI: 10.3389/fcell.2022.932297

关键词

adult neurogenesis; calretinin neuron subtypes; morphology; olfactory bulb layers; 3D analysis; transcription factors

资金

  1. Spanish Ministerio de Economia y Competitividad and Ministerio de Ciencia e Innovacion (MICINN) [SAF 2013-4759R, SAF 2016-80419-R, PID 2019-109059RB-100, CIBERNED CB06/05/0065]
  2. Comunidad de Madrid [S2011/BMD-2336]
  3. CSIC Intramural program [201220E098, 201320E054]
  4. Spanish Ministerio de Economia y Competitividad and Ministerio de Ciencia e Innovacion (MINECO)

向作者/读者索取更多资源

This study found that neural stem cells in the olfactory bulb of adult mice can generate CalR(+) neurons, and these adult cells exhibit different morphologies when migrating to different layers of the olfactory bulb. The study also revealed that altering the expression of the transcription factor Tbr1 can affect the migration and morphology of these newly generated neurons.
Neural stem cells (NSCs) in the olfactory bulb (OB) core can generate mature interneurons in the adult mice brain. The vast majority of these adult generated cells express the calcium-binding protein Calretinin (CalR), and they migrate towards different OB layers. However, these cells have yet to be fully characterized and hence, to achieve this we injected retroviral particles expressing GFP into the OB core of adult animals and found that the CalR(+) neurons generated from NSCs mainly migrate to the granule cell layer (GCL) and glomerular layer (GL) in similar proportions. In addition, since morphology and function are closely related, we used three-dimensional imaging techniques to analyze the morphology of these adult born cells, describing new subtypes of CalR(+) interneurons based on their dendritic arborizations and projections, as well as their localization in the GCL or GL. We also show that the migration and morphology of these newly generated neurons can be altered by misexpressing the transcription factor Tbr1 in the OB core. Therefore, the morphology acquired by neurons located in a specific OB layer is the result of a combination of both extrinsic (e.g., layer allocation) and intrinsic mechanisms (e.g., transcription factors). Defining the cellular processes and molecular mechanisms that govern adult neurogenesis might help better understand brain circuit formation and plasticity, as well as eventually opening the way to develop strategies for brain repair.

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