Dhillon Sandeep S, Belsham Denise D
Departments of Physiology, Obstetrics and Gynaecology and Medicine, University of Toronto, ON, Canada.
Regul Pept. 2011 Apr 11;167(2-3):192-200. doi: 10.1016/j.regpep.2011.01.005. Epub 2011 Jan 22.
Leptin acts as a key peripheral hormone in distinct neurons in the hypothalamus to modulate both reproductive function and energy homeostasis. The control of neuropeptide Y (NPY) secretion is an example of a process that can be differentially regulated by leptin. In order to further understand these distinct modulatory effects, we have used immortalized, neuronal hypothalamic cell lines expressing NPY, mHypoE-38 and mHypoE-46. We found that these cell lines express the endogenous leptin receptor, ObRb, and secrete detectable levels of NPY. We exposed the neurons to 100nM leptin for 1h and determined that the basal levels of NPY in the cell lines were differentially regulated: NPY secretion was inhibited in mHypoE-46 neurons, whereas NPY secretion was induced in the mHypoE-38 neurons. In order to determine the mechanisms involved in the divergent regulation of NPY release, we analyzed the activity of a number of signaling components using phospho-specific antibodies directed towards specific proteins in the MAP kinase, PI3K, and AMPK pathways, among others. We found that leptin activated a different combination of second messengers in each cell line. Importantly, we could link the regulation of NPY secretion to different signaling pathways, AMPK in the mHypoE-46 and both MAPK and PI3K in the mHypoE-38 neurons. This is the first demonstration that leptin can specifically regulate individual NPY neuron secretory responses through distinct signaling pathways.
瘦素作为一种关键的外周激素,作用于下丘脑的不同神经元,调节生殖功能和能量平衡。神经肽Y(NPY)分泌的控制就是一个可被瘦素差异性调节的过程实例。为了进一步了解这些不同的调节作用,我们使用了表达NPY的永生化下丘脑神经元细胞系mHypoE - 38和mHypoE - 46。我们发现这些细胞系表达内源性瘦素受体ObRb,并分泌可检测水平的NPY。我们将这些神经元暴露于100nM瘦素中1小时,确定细胞系中NPY的基础水平受到差异性调节:mHypoE - 46神经元中的NPY分泌受到抑制,而mHypoE - 38神经元中的NPY分泌则被诱导。为了确定参与NPY释放差异性调节的机制,我们使用针对MAP激酶、PI3K和AMPK等途径中特定蛋白质的磷酸化特异性抗体,分析了多种信号成分的活性。我们发现瘦素在每个细胞系中激活了不同组合的第二信使。重要的是,我们可以将NPY分泌的调节与不同的信号通路联系起来,mHypoE - 46中的AMPK以及mHypoE - 38神经元中的MAPK和PI3K。这是首次证明瘦素可通过不同的信号通路特异性调节单个NPY神经元的分泌反应。