4.7 Article

5T4 Glycoprotein Regulates the Sensory Input-Dependent Development of a Specific Subtype of Newborn Interneurons in the Mouse Olfactory Bulb

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JOURNAL OF NEUROSCIENCE
卷 32, 期 6, 页码 2217-2226

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SOC NEUROSCIENCE
DOI: 10.1523/JNEUROSCI.5907-11.2012

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资金

  1. Ministry of Education, Culture, Sports, Science and Technology (MEXT), Japan
  2. Naito
  3. Novartis
  4. Terumo
  5. Applied Enzymology
  6. Urakami
  7. Mishimakaiun Memorial Foundation
  8. Uehara Memorial Foundation
  9. Daiwa Housing Group
  10. MEXT
  11. Kao Foundation for Arts and Sciences, Japan
  12. Sumitomo
  13. Mochida Memorial
  14. Life Science
  15. Cosmetology
  16. Takeda Science Promotion Foundation, Japan
  17. Uehara Memorial and Inamori Foundations, Japan
  18. Cancer Research UK [C480/A12328]
  19. Grants-in-Aid for Scientific Research [22700409, 23122516, 22700341, 24650170] Funding Source: KAKEN

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Sensory input has been shown to regulate development in a variety of species and in various structures, including the retina, cortex, and olfactory bulb (OB). Within the mammalian OB specifically, the development of dendrites in mitral/tufted cells is well known to be odor-evoked activity dependent. However, little is known about the developmental role of sensory input in the other major OB population of the GABAgenic interneurons, such as granule cells and periglomerular cells. Here, we identified, with DNA microarray and in situ hybridization screenings, a trophoblast glycoprotein gene, 5T4, whose expression in a specific subtype of OB interneurons is dependent on sensory input. 5T4 is a type I membrane protein, whose extracellular domain contains seven leucine-rich repeats (LRR) flanked by characteristic LRR-N-flanking and C-flanking regions, and a cytoplasmic domain. 5T4 overexpression in the newborn OB interneurons facilitated their dendritic arborization even under the sensory input-deprived condition. By contrast, both 5T4 knockdown with RNAi and 5T4 knockout with mice resulted in a significant reduction in the dendritic arborization of 5T4(+) granule cells. Further, we identified the amino acid sequence in the 5T4 cytoplasmic domain that is necessary and sufficient for the sensory input-dependent dendritic shaping of specific neuronal subtypes in the OB. Thus, these results demonstrate that 5T4 glycoprotein contributes in the regulation of activity-dependent dendritic development of interneurons and the formation of functional neural circuitry in the OB.

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