The production of somatostatin interneurons in the olfactory bulb is regulated by the transcription factor sp8

PLoS One. 2013 Jul 23;8(7):e70049. doi: 10.1371/journal.pone.0070049. Print 2013.

Abstract

Somatostatin (Som), one of the most concentrated neuropeptides in the brain, is highly expressed in the olfactory bulb (OB). However, the temporal profile by which OB somatostatin-expressing (Som+) interneurons are produced and the molecular mechanisms controlling this profile are totally unknown. In the present study, we found that all the Som+ interneurons in the mouse external plexiform layer (EPL) and the rat glomerular layer (GL) express the transcription factor Sp8.Using the 5-bromo-2'-deoxyuridine (BrdU) birth dating method, combined with immunostaining, we showed that the generation of Som+ interneurons in the mouse and rat OB is confined to the later embryonic and earlier postnatal stages. Within the mouse OB, the production of Som+ interneurons is maximal during late embryogenesis and decreases after birth, whereas the generation of Som+ interneurons is low during embryogenesis and increases gradually after birth in the rat OB. Interestingly, genetic ablation of Sp8 by cre/loxP-based recombination severely reduces the number of Som+ interneurons in the EPL of the mouse OB. Taken together, these results suggest that Sp8 is required for the normal production of Som+ interneurons in the EPL of the mouse OB.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • DNA-Binding Proteins / biosynthesis*
  • Female
  • Immunohistochemistry
  • Interneurons / cytology*
  • Interneurons / metabolism*
  • Male
  • Mice
  • Olfactory Bulb / cytology*
  • Olfactory Bulb / embryology
  • Olfactory Bulb / metabolism*
  • Rats
  • Rats, Wistar
  • Somatostatin / biosynthesis*
  • Transcription Factors / biosynthesis*

Substances

  • DNA-Binding Proteins
  • Sp8 protein, mouse
  • Transcription Factors
  • Somatostatin

Grants and funding

This work was funded by the National Natural Science Foundation of China (30900425; 31121061; 30990261) and Shanghai Natural Science Foundation (13ZR1402700). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.