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1.
Cell Mol Life Sci ; 77(18): 3597-3609, 2020 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-31758234

RESUMEN

The bHLH transcription factor Olig2 is required for sequential cell fate determination of both motor neurons and oligodendrocytes and for progenitor proliferation in the central nervous system. However, the role of Olig2 in peripheral sensory neurogenesis remains unknown. We report that Olig2 is transiently expressed in the newly differentiated olfactory sensory neurons (OSNs) and is down-regulated in the mature OSNs in mice from early gestation to adulthood. Genetic fate mapping demonstrates that Olig2-expressing cells solely give rise to OSNs in the peripheral olfactory system. Olig2 depletion does not affect the proliferation of peripheral olfactory progenitors and the fate determination of OSNs, sustentacular cells, and the olfactory ensheathing cells. However, the terminal differentiation and maturation of OSNs are compromised in either Olig2 single or Olig1/Olig2 double knockout mice, associated with significantly diminished expression of multiple OSN maturation and odorant signaling genes, including Omp, Gnal, Adcy3, and Olfr15. We further demonstrate that Olig2 binds to the E-box in the Omp promoter region to regulate its expression. Taken together, our results reveal a distinctly novel function of Olig2 in the periphery nervous system to regulate the terminal differentiation and maturation of olfactory sensory neurons.


Asunto(s)
Diferenciación Celular , Neuronas Receptoras Olfatorias/metabolismo , Factor de Transcripción 2 de los Oligodendrocitos/metabolismo , Animales , Factores de Transcripción con Motivo Hélice-Asa-Hélice Básico/deficiencia , Factores de Transcripción con Motivo Hélice-Asa-Hélice Básico/genética , Factores de Transcripción con Motivo Hélice-Asa-Hélice Básico/metabolismo , Linaje de la Célula , Proliferación Celular , Proteína Doblecortina , Embrión de Mamíferos/metabolismo , Embrión de Mamíferos/patología , Ratones , Ratones Transgénicos , Proteína Marcadora Olfativa/genética , Mucosa Olfatoria/citología , Mucosa Olfatoria/metabolismo , Factor de Transcripción 2 de los Oligodendrocitos/deficiencia , Factor de Transcripción 2 de los Oligodendrocitos/genética , Regiones Promotoras Genéticas , Factores de Transcripción SOXB1/deficiencia , Factores de Transcripción SOXB1/genética , Tubulina (Proteína)/genética , Tubulina (Proteína)/metabolismo
3.
J Cell Sci ; 124(Pt 9): 1553-63, 2011 May 01.
Artículo en Inglés | MEDLINE | ID: mdl-21486944

RESUMEN

The mammalian olfactory epithelium (OE) has a unique stem cell or progenitor niche, which is responsible for the constant peripheral neurogenesis throughout the lifespan of the animal. However, neither the signals that regulate the behavior of these cells nor the lineage properties of the OE stem cells are well understood. Multiple Wnt signaling components exhibit dynamic expression patterns in the developing OE. We generated Wnt signaling reporter TOPeGFP transgenic mice and found TOPeGFP activation predominantly in proliferating Sox2(+) OE basal cells during early postnatal development. FACS-isolated TOPeGFP(+) OE basal cells are required, but are not sufficient, for formation of spheres. Wnt3a significantly promotes the proliferation of the Sox2(+) OE sphere cells. Wnt-stimulated OE sphere cells maintain their multipotency and can differentiate into most types of neuronal and non-neuronal epithelial cells. Also, Wnt activators shift the production of differentiated cells toward olfactory sensory neurons. Moreover, TOPeGFP(+) cells are robustly increased in the adult OE after injury. In vivo administration of Wnt modulators significantly alters the regeneration potential. This study demonstrates the role of the canonical Wnt signaling pathway in the regulation of OE stem cells or progenitors during development and regeneration.


Asunto(s)
Diferenciación Celular/fisiología , Neurogénesis/fisiología , Mucosa Olfatoria/citología , Células Madre/citología , Animales , Apoptosis/genética , Apoptosis/fisiología , Diferenciación Celular/genética , Proliferación Celular , Células Cultivadas , Citometría de Flujo , Inmunohistoquímica , Hibridación in Situ , Ratones , Ratones Transgénicos , Neurogénesis/genética , Neuronas/citología , Neuronas/metabolismo , Reacción en Cadena de la Polimerasa de Transcriptasa Inversa , Factores de Transcripción SOXB1/genética , Factores de Transcripción SOXB1/metabolismo , Transducción de Señal/genética , Transducción de Señal/fisiología , Proteínas Wnt/genética , Proteínas Wnt/metabolismo , Proteína Wnt3 , Proteína Wnt3A
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