Adult neurogenesis and specific replacement of interneuron subtypes in the mouse main olfactory bulb
Autor: | Nathaniel N. Urban, Joshua A. Bagley, Greg LaRocca, Daniel A. Jimenez |
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Rok vydání: | 2007 |
Předmět: |
Calbindins
Tyrosine 3-Monooxygenase Interneuron Rostral migratory stream Subventricular zone Nerve Tissue Proteins S100 Calcium Binding Protein beta Subunit Biology lcsh:RC321-571 Mice 03 medical and health sciences Cellular and Molecular Neuroscience S100 Calcium Binding Protein G 0302 clinical medicine Neuroblast Cell Movement Interneurons medicine Animals Nerve Growth Factors lcsh:Neurosciences. Biological psychiatry. Neuropsychiatry Cellular Senescence gamma-Aminobutyric Acid 030304 developmental biology 0303 health sciences General Neuroscience Calcium-Binding Proteins S100 Proteins lcsh:QP351-495 Neurogenesis Nuclear Proteins Granule cell Olfactory Bulb Olfactory bulb DNA-Binding Proteins Mice Inbred C57BL Adult Stem Cells lcsh:Neurophysiology and neuropsychology medicine.anatomical_structure Bromodeoxyuridine Microscopy Fluorescence nervous system Calbindin 2 Calreticulin Neuroscience Biomarkers 030217 neurology & neurosurgery Research Article Adult stem cell |
Zdroj: | BMC Neuroscience, Vol 8, Iss 1, p 92 (2007) BMC Neuroscience |
ISSN: | 1471-2202 |
Popis: | Background New neurons are generated in the adult brain from stem cells found in the subventricular zone (SVZ). These cells proliferate in the SVZ, generating neuroblasts which then migrate to the main olfactory bulb (MOB), ending their migration in the glomerular layer (GLL) and the granule cell layer (GCL) of the MOB. Neuronal populations in these layers undergo turnover throughout life, but whether all neuronal subtypes found in these areas are replaced and when neurons begin to express subtype-specific markers is not known. Results Here we use BrdU injections and immunohistochemistry against (calretinin, calbindin, N-copein, tyrosine hydroxylase and GABA) and show that adult-generated neurons express markers of all major subtypes of neurons in the GLL and GCL. Moreover, the fractions of new neurons that express subtype-specific markers at 40 and 75 days post BrdU injection are very similar to the fractions of all neurons expressing these markers. We also show that many neurons in the glomerular layer do not express NeuN, but are readily and specifically labeled by the fluorescent nissl stain Neurotrace. Conclusion The expression of neuronal subtype-specific markers by new neurons in the GLL and GCL changes rapidly during the period from 14–40 days after BrdU injection before reaching adult levels. This period may represent a critical window for cell fate specification similar to that observed for neuronal survival. |
Databáze: | OpenAIRE |
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