The interfascicular trigeminal nucleus: A precerebellar nucleus in the mouse defined by retrograde neuronal tracing and genetic fate mapping. Issue 3 (17th December 2012)

• Record Type: Journal Article
• Authors: Fu, Yuhong; Tvrdik, Petr; Makki, Nadja; Machold, Robert; Paxinos, George; Watson, Charles
• Is Part Of: Journal of comparative neurology. Volume 521:Issue 3(2013:Feb. 15)
• Page Start: 697
• Page End: 708
• Publication Date: 2012-12-17
• Subjects: Comparative neurobiology -- Periodicals; Neurology -- Periodicals; 616
• DOI: 10.1002/cne.23200
• Languages: English
• ISSNs: 0021-9967

Abstract

<abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>We have found a previously unreported precerebellar nucleus located among the emerging fibers of the motor root of the trigeminal nerve in the mouse, which we have called the interfascicular trigeminal nucleus (IF5). This nucleus had previously been named the tensor tympani part of the motor trigeminal nucleus (5TT) in rodent brain atlases, because it was thought to be a subset of small motor neurons of the motor trigeminal nucleus innervating the tensor tympani muscle. However, following injection of retrograde tracer in the cerebellum, the labeled neurons in IF5 were found to be choline acetyltransferase (ChAT) negative, indicating that they are not motor neurons. The cells of IF5 are strongly labeled in mice from <italic>Wnt1</italic>Cre and <italic>Atoh1</italic> CreER lineage fate mapping, in common with the major precerebellar nuclei that arise from the rhombic lip and that issue mossy fibers. Analysis of sections from mouse <italic>Hoxa3</italic>, <italic>Hoxb1</italic>, and <italic>Egr2</italic> Cre labeled lineages shows that the neurons of IF5 arise from rhombomeres caudal to rhombomere 4, most likely from rhombomeres 6–8. We conclude that IF5 is a significant precerebellar nucleus in the mouse that shares developmental gene expression characteristics with mossy fiber precerebellar nuclei that arise from the caudal rhombic lip. J. Comp. Neurol. 521:697–708, 2013. © 2012 Wiley Periodicals, Inc.</p> </abstract>