Gonadotropin-releasing hormone (GnRH) neurons are born in the nasal placode and migrate along olfactory and vomeronasal axons to reach the forebrain and settle in the hypothalamus, where they control reproduction. The molecular cues that guide their migration have not been fully identified, but are thought to control either cell movement directly or the patterning of their axonal substrates. Using genetically altered mouse models we show that the migration of GnRH neurons is directly modulated by Slit2 and Robo3, members of the axon guidance Slit ligand and Robo receptor families. Mice lacking Slit2 or Robo3 have a reduced number of GnRH neurons in the forebrain, but a normal complement of their supporting axons, pointing to a direct role for these molecules in GnRH neuron migration.

Slit2 and Robo3 modulate the migration of GnRH-secreting neurons / A. Cariboni, W.D. Andrews, F. Memi, A.R. Ypsilanti, P. Zelina, A. Chedotal, J.G. Parnavelas. - In: DEVELOPMENT. - ISSN 0950-1991. - 139:18(2012 Sep), pp. 3326-3331. [10.1242/dev.079418]

Slit2 and Robo3 modulate the migration of GnRH-secreting neurons

A. Cariboni
Primo
;
2012

Abstract

Gonadotropin-releasing hormone (GnRH) neurons are born in the nasal placode and migrate along olfactory and vomeronasal axons to reach the forebrain and settle in the hypothalamus, where they control reproduction. The molecular cues that guide their migration have not been fully identified, but are thought to control either cell movement directly or the patterning of their axonal substrates. Using genetically altered mouse models we show that the migration of GnRH neurons is directly modulated by Slit2 and Robo3, members of the axon guidance Slit ligand and Robo receptor families. Mice lacking Slit2 or Robo3 have a reduced number of GnRH neurons in the forebrain, but a normal complement of their supporting axons, pointing to a direct role for these molecules in GnRH neuron migration.
GnRH neuron; Neuronal migration; Reproduction; Robo3; Slit2
Settore BIO/13 - Biologia Applicata
set-2012
Article (author)
File in questo prodotto:
File Dimensione Formato  
3326.full.pdf

accesso aperto

Tipologia: Publisher's version/PDF
Dimensione 3.3 MB
Formato Adobe PDF
3.3 MB Adobe PDF Visualizza/Apri
Pubblicazioni consigliate

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/208643
Citazioni
  • ???jsp.display-item.citation.pmc??? 10
  • Scopus 23
  • ???jsp.display-item.citation.isi??? 23
social impact