Neural Stem Cells in the Adult Olfactory Bulb Core Generate Mature Neurons in Vivo

Author:

Defteralı Çağla12,Moreno-Estellés Mireia34,Crespo Carlos5,Díaz-Guerra Eva12,Díaz-Moreno María3,Vergaño-Vera Eva12,Nieto-Estévez Vanesa12,Hurtado-Chong Anahí12,Consiglio Antonella67,Mira Helena34,Vicario Carlos12ORCID

Affiliation:

1. Instituto Cajal-Consejo Superior de Investigaciones Científicas (CSIC), Madrid, Spain

2. CIBERNED-Instituto de Salud Carlos III (ISCIII), Madrid, Spain

3. Unidad de Neurobiología Molecular  Área de Biología Celular y del Desarrollo, CNM-ISCIII, Majadahonda, Spain

4. Instituto de Biomedicina de Valencia-CSIC (IBV-CSIC), Valencia, Spain

5. Departamento de Biología Celular  Estructura de Investigación Interdisciplinar en Biotecnología y Biomedicina (BIOTECMED), Universitat de Valencia, Valencia, Spain

6. Institute of Biomedicine, Department of Pathology and Experimental Therapeutics  Bellvitge University Hospital-IDIBELL, Barcelona, Spain

7. Department of Molecular and Translational Medicine  University of Brescia, Brescia, Italy

Abstract

Abstract Although previous studies suggest that neural stem cells (NSCs) exist in the adult olfactory bulb (OB), their location, identity, and capacity to generate mature neurons in vivo has been little explored. Here, we injected enhanced green fluorescent protein (EGFP)-expressing retroviral particles into the OB core of adult mice to label dividing cells and to track the differentiation/maturation of any neurons they might generate. EGFP-labeled cells initially expressed adult NSC markers on days 1 to 3 postinjection (dpi), including Nestin, GLAST, Sox2, Prominin-1, and GFAP. EGFP+-doublecortin (DCX) cells with a migratory morphology were also detected and their abundance increased over a 7-day period. Furthermore, EGFP-labeled cells progressively became NeuN+ neurons, they acquired neuronal morphologies, and they became immunoreactive for OB neuron subtype markers, the most abundant representing calretinin expressing interneurons. OB-NSCs also generated glial cells, suggesting they could be multipotent in vivo. Significantly, the newly generated neurons established and received synaptic contacts, and they expressed presynaptic proteins and the transcription factor pCREB. By contrast, when the retroviral particles were injected into the subventricular zone (SVZ), nearly all (98%) EGFP+-cells were postmitotic when they reached the OB core, implying that the vast majority of proliferating cells present in the OB are not derived from the SVZ. Furthermore, we detected slowly dividing label-retaining cells in this region that could correspond to the population of resident NSCs. This is the first time NSCs located in the adult OB core have been shown to generate neurons that incorporate into OB circuits in vivo.

Funder

Comunidad de Madrid

Consejo Superior de Investigaciones Científicas

Generalitat Valenciana

Instituto de Salud Carlos III

Secretaría de Estado de Investigación, Desarrollo e Innovación

Publisher

Oxford University Press (OUP)

Subject

Cell Biology,Developmental Biology,Molecular Medicine

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