4.3 Article

Somatostatin affects GnRH neuronal development and migration and stimulates olfactory-related fiber fasciculation

Journal

DEVELOPMENTAL NEUROBIOLOGY
Volume -, Issue -, Pages -

Publisher

WILEY
DOI: 10.1002/dneu.22931

Keywords

GnRH neurons; neuronal migration; olfactory placode; olfactory-related fibers; siRNA; somatostatin

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The expression of somatostatin (SST) in the olfactory epithelium and nerves of chick embryos during embryonic days 5-8 suggests its involvement in the development and migration of GnRH neurons. Suppression of SST mRNA in chick embryos reduced the number of GnRH neurons in the nasal region without affecting their entry into the forebrain. SST treatment increased the number and migration distance of GnRH neurons in OP explant cultures, and SST antagonist blocked these effects. Furthermore, SST was found to facilitate the fasciculation of olfactory-related fibers.
Transient expression of somatostatin (SST) has been observed in the olfactory epithelium (OE) and nerves of chick embryos. Intense expression of SST in these regions on embryonic days (E) 5-8 coincides with the migration of neurons producing gonadotropin-releasing hormone (GnRH) from the OE to the forebrain (FB), suggesting that SST plays a role in the development of GnRH neurons. Using in ovo electroporation of small interfering RNA, we found that the suppression of SST mRNA in the olfactory placode (OP) of E3.5 chick embryos significantly reduced the number of GnRH and Islet-1-immunoreactive neurons in the nasal region without affecting the entry of GnRH neurons into the FB at E5.5-6. SST knockdown did not lead to changes in the number of apoptotic, proliferating, or HuC/D-positive neuronal cells in the OE; therefore, it is possible that SST is involved in the neurogenesis/differentiation of GnRH neurons and OP-derived GnRH-negative migratory neurons. In whole OP explant cultures, we also found that SST or its analog octreotide treatment significantly increased the number of migratory GnRH neurons and the migratory distance from the explants. The co-application of an SST antagonist blocked the octreotide-induced increase in the number of GnRH neurons. Furthermore, the fasciculation of polysialylated neural cell adhesion molecule-immunoreactive fibers emerging from the explants was dependent on octreotide. Taken together, our results provide evidence that SST exerts facilitatory effects on the development of neurons expressing GnRH or Islet-1 and on GnRH neuronal migration, in addition to olfactory-related fiber fasciculation.

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