Bcl11b/Ctip2 Controls the Differentiation of Vomeronasal Sensory Neurons in Mice

• Published in: The Journal of neuroscience Vol. 31; no. 28; pp. 10159 - 10173
• Main Authors: Enomoto, T., Ohmoto, M., Iwata, T., Uno, A., Saitou, M., Yamaguchi, T., Kominami, R., Matsumoto, I., Hirota, J.
• Format: Journal Article
• Language: English
• Published: United States Society for Neuroscience 13.07.2011
• Subjects: Animals; Cell Differentiation - physiology; gamma-Aminobutyric Acid - metabolism; Interneurons - metabolism; Mice; Mice, Knockout; Olfactory Bulb - cytology; Olfactory Bulb - metabolism; Repressor Proteins - metabolism; Sensory Receptor Cells - metabolism; Tumor Suppressor Proteins - metabolism; Vomeronasal Organ - cytology; Vomeronasal Organ - metabolism
• ISSN: 0270-6474; 1529-2401; 1529-2401
• DOI: 10.1523/JNEUROSCI.1245-11.2011

The transcription factor Bcl11b/Ctip2 plays critical roles in the development of several systems and organs, including the immune system, CNS, skin, and teeth. Here, we show that Bcl11b/Ctip2 is highly expressed in the developing vomeronasal system in mice and is required for its proper development. Bcl11b/Ctip2 is expressed in postmitotic vomeronasal sensory neurons (VSNs) in the vomeronasal epithelium (VNE) as well as projection neurons and GABAergic interneurons in the accessory olfactory bulb (AOB). In the absence of Bcl11b, these neurons are born in the correct number, but VSNs selectively die by apoptosis. The critical role of Bcl11b in vomeronasal system development is demonstrated by the abnormal phenotypes of Bcl11b-deficient mice: disorganization of layer formation of the AOB, impaired axonal projections of VSNs, a significant reduction in the expression of vomeronasal receptor genes, and defective mature differentiation of VSNs. VSNs can be classified into two major types of neurons, vomeronasal 1 receptor (V1r)/Gα(i2)-positive and vomeronasal 2 receptor (V2r)/Gα(o)-positive VSNs. We found that all Gα(i2)-positive cells coexpressed Gα(o) during embryogenesis. This coexpression is also observed in newly differentiated neurons in the adult VNE. Interestingly, loss of Bcl11b function resulted in an increased number of V1r/Gα(i2)-type VSNs and a decreased number of V2r/Gα(o)-type VSNs, suggesting that Bcl11b regulates the fate choice between these two VSN types. These results indicate that Bcl11b/Ctip2 is an essential regulator of the differentiation and dichotomy of VSNs.