Bonfiglio Juan J, Inda Carolina, Senin Sergio, Maccarrone Giuseppina, Refojo Damián, Giacomini Damiana, Turck Christoph W, Holsboer Florian, Arzt Eduardo, Silberstein Susana
Instituto de Investigación en Biomedicina de Buenos Aires (IBioBA), CONICET, Partner Institute of the Max Planck Society, Godoy Cruz 2390, C1425FQA Buenos Aires, Argentina.
Mol Endocrinol. 2013 Mar;27(3):491-510. doi: 10.1210/me.2012-1359. Epub 2013 Jan 31.
CRH is a key regulator of neuroendocrine, autonomic, and behavioral response to stress. CRH-stimulated CRH receptor 1 (CRHR1) activates ERK1/2 depending on intracellular context. In a previous work, we demonstrated that CRH activates ERK1/2 in limbic areas of the mouse brain (hippocampus and basolateral amygdala). ERK1/2 is an essential mediator of hippocampal physiological processes including emotional behavior, synaptic plasticity, learning, and memory. To elucidate the molecular mechanisms by which CRH activates ERK1/2 in hippocampal neurons, we used the mouse hippocampal cell line HT22. We document for the first time that ERK1/2 activation in response to CRH is biphasic, involving a first cAMP- and B-Raf-dependent early phase and a second phase that critically depends on CRHR1 internalization and β-arrestin2. By means of mass-spectrometry-based screening, we identified B-Raf-associated proteins that coimmunoprecipitate with endogenous B-Raf after CRHR1 activation. Using molecular and pharmacological tools, the functional impact of selected B-Raf partners in CRH-dependent ERK1/2 activation was dissected. These results indicate that 14-3-3 proteins, protein kinase A, and Rap1, are essential for early CRH-induced ERK1/2 activation, whereas dynamin and vimentin are required for the CRHR1 internalization-dependent phase. Both phases of ERK1/2 activation depend on calcium influx and are affected by calcium/calmodulin-dependent protein kinase II inactivation. Thus, this report describes the dynamics and biphasic nature of ERK1/2 activation downstream neuronal CRHR1 and identifies several new critical components of the CRHR1 signaling machinery that selectively controls the early and late phases of ERK1/2 activation, thus providing new potential therapeutic targets for stress-related disorders.
促肾上腺皮质激素释放激素(CRH)是对应激的神经内分泌、自主神经和行为反应的关键调节因子。CRH刺激的促肾上腺皮质激素释放激素受体1(CRHR1)根据细胞内环境激活细胞外调节蛋白激酶1/2(ERK1/2)。在之前的一项研究中,我们证明CRH可激活小鼠脑海马和基底外侧杏仁核等边缘区域的ERK1/2。ERK1/2是海马生理过程(包括情绪行为、突触可塑性、学习和记忆)的重要介导因子。为阐明CRH在海马神经元中激活ERK1/2的分子机制,我们使用了小鼠海马细胞系HT22。我们首次证明,CRH诱导的ERK1/2激活是双相的,包括第一个依赖于环磷酸腺苷(cAMP)和B-Raf的早期阶段以及第二个关键依赖于CRHR1内化和β-抑制蛋白2的阶段。通过基于质谱的筛选,我们鉴定了CRHR1激活后与内源性B-Raf共免疫沉淀的B-Raf相关蛋白。使用分子和药理学工具,剖析了所选B-Raf伴侣在CRH依赖性ERK1/2激活中的功能影响。这些结果表明,14-3-3蛋白、蛋白激酶A和Rap1对早期CRH诱导的ERK1/2激活至关重要,而发动蛋白和波形蛋白是CRHR1内化依赖性阶段所必需的。ERK1/2激活的两个阶段均依赖于钙内流,并受钙/钙调蛋白依赖性蛋白激酶II失活的影响。因此,本报告描述了神经元CRHR1下游ERK1/2激活的动态变化和双相性质,并鉴定了CRHR1信号传导机制中的几个新的关键成分,这些成分选择性地控制ERK1/2激活的早期和晚期阶段,从而为应激相关疾病提供了新的潜在治疗靶点。