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[Abstract Title]. - Society for Neuroscience

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Program#/Poster#: 231.6/B19<br />

Topic: A.04.i. Dendritic growth and branching<br />

Support: NIH Grant DC000210<br />

NIH Grant DC006972<br />

NIH Grant DC006291<br />

<strong>Title</strong>: Role of TrkB in dendritic development of mitral cells in mouse olfactory bulb<br />

Authors: *F. IMAMURA, C. GREER;<br />

Dept. Neurosurg., Yale Univ,Sch Med., New Haven, CT<br />

<strong>Abstract</strong>: Mature mitral and tufted cells in the mammalian olfactory bulb (OB) have a single<br />

primary dendrite that arborizes within a single glomerulus. Here, we focused on factors<br />

regulating the development of mitral/tufted cell dendritic arbors within a glomerulus, and test the<br />

hypothesis that the neurotrophins are important determinants of this mechanism. First, we<br />

visualized the development of glomerular tufts of mitral cells in mice using intracellular lucifer<br />

yellow injections. We found that dendritic tufts in a glomerulus significantly increase their total<br />

length and number of branching points during early postnatal days, especially from postnatal day<br />

(P) 3 to 10. Second, using immunohistochemical analyses, we found that the full-length TrkB<br />

(TrkB.FL) was expressed by thick dendritic trunks of mitral/tufted cells, while the truncated<br />

iso<strong>for</strong>m of TrkB (TrkB.T1) is localized at the tip of mitral/tufted cell dendrites including<br />

dendritic tips in the glomerular tuft. Interestingly, the TrkB.T1 expression in glomeruli<br />

colocalized with growth cone marker CDA 1, and was high during early postnatal days but<br />

disappeared by P10. There<strong>for</strong>e, this suggested that the TrkB.T1 was expressed in dendritic<br />

growth cones when dendrites arborize in glomeruli. Third, to examine the role of TrkB in<br />

dendritic development, we cultured mitral/tufted cells and treated them with neurotrophins:<br />

BDNF, NT-3, and NT-4. In cultured mitral/tufted cells at 1 day in vitro (DIV), localization of the<br />

TrkB.T1 at the tip of neurites was observed, while the TrkB.FL was seen in whole neurites.<br />

When treated with TrkB ligands, BDNF or NT-4, from 0 to 4 DIV, mitral/tufted cells<br />

significantly increased the number of primary neurites and branching points, as well as their total<br />

neurite length compared with untreated controls. NT-3 treatment did not have a significant<br />

effect. Our findings strongly suggest that the TrkB.T1 expression during dendritic development<br />

plays a significant role in the elaboration of mitral/tufted cell glomerular dendritic arbors,<br />

consistent with our working hypothesis that neurotrophins are determinants of olfactory bulb<br />

circuitry.<br />

Disclosures: F. Imamura, None; C. Greer, None.<br />

Poster

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