4.6 Article

Crypto-rhombomeres of the mouse medulla oblongata, defined by molecular and morphological features

Journal

BRAIN STRUCTURE & FUNCTION
Volume 221, Issue 2, Pages 815-838

Publisher

SPRINGER HEIDELBERG
DOI: 10.1007/s00429-014-0938-y

Keywords

Rhombomeres; Medulla oblongata; Hox; Brain segmentation; Neuromeres; Sensory columns

Funding

  1. Fundacion Seneca of the Government of the Murcia Region [04548-GERM-06]
  2. Spanish Ministry of Science and Innovation [MICINN-BFU2008-04156]
  3. Fundacion Seneca
  4. NICHD

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The medulla oblongata is the caudal portion of the vertebrate hindbrain. It contains major ascending and descending fiber tracts as well as several motor and interneuron populations, including neural centers that regulate the visceral functions and the maintenance of bodily homeostasis. In the avian embryo, it has been proposed that the primordium of this region is subdivided into five segments or crypto-rhombomeres (r7-r11), which were defined according to either their parameric position relative to intersomitic boundaries (Cambronero and Puelles, in J Comp Neurol 427:522-545, 2000) or a stepped expression of Hox genes (Marin et al., in Dev Biol 323:230-247, 2008). In the present work, we examine the implied similar segmental organization of the mouse medulla oblongata. To this end, we analyze the expression pattern of Hox genes from groups 3 to 8, comparing them to the expression of given cytoarchitectonic and molecular markers, from mid-gestational to perinatal stages. As a result of this approach, we conclude that the mouse medulla oblongata is segmentally organized, similarly as in avian embryos. Longitudinal structures such as the nucleus of the solitary tract, the dorsal vagal motor nucleus, the hypoglossal motor nucleus, the descending trigeminal and vestibular columns, or the reticular formation appear subdivided into discrete segmental units. Additionally, our analysis identified an internal molecular organization of the migrated pontine nuclei that reflects a differential segmental origin of their neurons as assessed by Hox gene expression.

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