Banerjee Sunayana B, Rajendran Rajeev, Dias Brian G, Ladiwala Uma, Tole Shubha, Vaidya Vidita A
Department of Biological Sciences, Tata Institute of Fundamental Research, Mumbai 400005, India.
Eur J Neurosci. 2005 Oct;22(7):1570-80. doi: 10.1111/j.1460-9568.2005.04317.x.
Electroconvulsive seizure (ECS) induces structural remodelling in the adult mammalian brain, including an increase in adult hippocampal neurogenesis. The molecular mechanisms that underlie this increase in the proliferation of adult hippocampal progenitors are at present not well understood. We hypothesized that ECS may recruit the Sonic hedgehog (Shh) pathway to mediate its effects on adult hippocampal neurogenesis, as Shh is known to enhance the proliferation of neuronal progenitors and is expressed in the adult basal forebrain, a region that sends robust projections to the hippocampus. Here we demonstrate that the ECS-induced increase in proliferation of adult hippocampal progenitors was completely blocked in animals treated with cyclopamine, a pharmacological inhibitor of Shh signalling. Our results suggest that both acute and chronic ECS enhance Shh signalling in the adult hippocampus, as we observed a robust upregulation of Patched (Ptc) mRNA, a component of the Shh receptor complex and a downstream transcriptional target of Shh signalling. This increase was rapid and restricted to the dentate gyrus, where the adult hippocampal progenitors reside. In addition, both acute and chronic ECS decreased Smoothened (Smo) mRNA, the other component of the Shh receptor complex, selectively within the dentate gyrus. However, ECS did not appear to influence Shh expression within the basal forebrain, the site from which it has been suggested to be anterogradely transported to the hippocampus. Together, our findings demonstrate that ECS regulates the Shh signalling cascade and indicate that the Shh pathway may be an important mechanism through which ECS enhances adult hippocampal neurogenesis.
电惊厥发作(ECS)可诱导成年哺乳动物大脑发生结构重塑,包括成年海马神经发生增加。目前,成年海马祖细胞增殖增加背后的分子机制尚不清楚。我们推测,ECS可能通过招募音猬因子(Shh)信号通路来介导其对成年海马神经发生的影响,因为已知Shh可增强神经元祖细胞的增殖,且在成年基底前脑表达,该区域向海马发出大量投射。在此,我们证明,在用环杷明(一种Shh信号通路的药理学抑制剂)处理的动物中,ECS诱导的成年海马祖细胞增殖增加被完全阻断。我们的结果表明,急性和慢性ECS均可增强成年海马中的Shh信号通路,因为我们观察到Shh受体复合物的一个组分及Shh信号通路的下游转录靶点——patched(Ptc)mRNA显著上调。这种增加迅速且局限于成年海马祖细胞所在的齿状回。此外,急性和慢性ECS均选择性地降低了齿状回内Shh受体复合物的另一个组分—— smoothened(Smo)mRNA的水平。然而,ECS似乎并未影响基底前脑内Shh的表达,而此前有观点认为Shh是从基底前脑顺行运输至海马的。总之,我们的研究结果表明ECS可调节Shh信号级联反应,并提示Shh信号通路可能是ECS增强成年海马神经发生的重要机制。