Department of Clinical Neurobiology, Heidelberg University Medical Center, 69120 Heidelberg, Germany; Department of Clinical Neurobiology/A230, German Center for Cancer Research (DKFZ), 69120 Heidelberg, Germany.
Neuron. 2013 Sep 18;79(6):1136-51. doi: 10.1016/j.neuron.2013.07.011. Epub 2013 Aug 29.
Neurogenesis underlies plastic changes in defined neuronal circuits in the postnatal and adult brain. Here we identify connective tissue growth factor (CTGF) as a critical factor in the mouse olfactory bulb (OB) in determining the efficiency of incorporation of postnatally born inhibitory neurons, thus gating the output of glomeruli, the first relay station of olfactory processing in the brain. In the OB, CTGF expression was restricted to prenatally born external tufted cells. CTGF enhanced the proapoptotic activity of glial-derived TGF-β2, decreasing the survival of periglomerular inhibitory neurons. Changes in CTGF expression levels in the OB led to modifications in local neuronal circuitry and olfactory behaviors. We show that the odorant-specific recruitment of distinct glomeruli resulted in enhanced local CTGF expression levels in the activated glomeruli. Collectively our data reveal a molecular mechanism controlling the survival of defined postnatally born neurons, thus adapting neuronal integration to the sensory experiences.
神经发生是出生后和成年大脑中特定神经元回路可塑性变化的基础。在这里,我们确定结缔组织生长因子 (CTGF) 是小鼠嗅球 (OB) 中的一个关键因素,决定了出生后抑制性神经元整合效率,从而控制了作为大脑中嗅觉处理第一中继站的肾小球的输出。在 OB 中,CTGF 的表达局限于出生前的外部丛状细胞。CTGF 增强了胶质衍生的 TGF-β2 的促凋亡活性,减少了周细胞抑制性神经元的存活。OB 中 CTGF 表达水平的变化导致局部神经元回路和嗅觉行为的改变。我们表明,不同肾小球的特定气味募集导致激活肾小球中局部 CTGF 表达水平的增强。总的来说,我们的数据揭示了一种控制特定出生后神经元存活的分子机制,从而使神经元整合适应感觉体验。