LIFRβ plays a major role in neuronal identity determination and glial differentiation in the mouse facial nucleus

• Published in: Developmental biology 2008, Vol.313 (1), p.267-278
• Main Authors: Alfonsi, Fabienne, Filippi, Pierre, Salaun, Danièle, deLapeyrière, Odile, Durbec, Pascale
• Format: Article
• Language: English
• Subjects: Animals; Astrocyte; Astrocytes - cytology; Cell Differentiation; Cellular Biology; Cytokine; Embryo, Mammalian - metabolism; Facial Nerve - cytology; Facial nucleus; Gene Expression Regulation, Developmental; Hindbrain development; Life Sciences; lifrβ mutant mice; Mice; Motor neuron; Neuroglia - cytology; Neurons - cytology; Oligodendrocyte; Oligodendroglia - cytology; Rhombencephalon - cytology; Rhombencephalon - embryology
• ISSN: 0012-1606; 1095-564X
• DOI: 10.1016/j.ydbio.2007.10.020

In the hindbrain, generation of the facial nucleus involves complex developmental processes that will lead to the formation of a structure composed of motor neurons, astrocytes and oligodendrocytes. The implication of LIF-related cytokines in the development of this nucleus came to light with the analysis of mice mutant for the receptor of these cytokines, LIFRβ, which exhibit a massive loss of facial branchiomotor (fbm) neurons at birth and a severe decrease in GFAP expression, a marker of astrocytes. To uncover the cellular mechanisms regulated by LIFRβ during facial nucleus development, we first analyzed its expression pattern in the hindbrain. lifrβ is first expressed at E11.5 in the hindbrain neuroepithelium. The receptor is absent during the migration of fbm post-mitotic neurons but is strongly expressed when fbm neurons have reached rhombomere 6 at E12.5, and its expression is maintained until E18.5. From the analysis of lifrβ mutant embryos, we established that LIFRβ is necessary for fbm neurons’ identity determination. We also show that LIFRβ is implicated in astrocyte and oligodendrocyte differentiation, specifically within the facial nucleus.