Ferrer Isidre, Mohan Pooja, Chen Helen, Castellsague Joan, Gómez-Baldó Laia, Carmona Marga, García Nadia, Aguilar Helena, Jiang Jihong, Skowron Margaretha, Nellist Mark, Ampuero Israel, Russi Antonio, Lázaro Conxi, Maxwell Christopher A, Pujana Miguel Angel
Institute of Neuropathology, University Hospital Bellvitge, University of Barcelona, Bellvitge Institute for Biomedical Research (IDIBELL), CIBERNED, L'Hospitalet del Llobregat, Barcelona, Catalonia, Spain.
J Pathol. 2014 Jul;233(3):247-57. doi: 10.1002/path.4343. Epub 2014 Apr 29.
Most patients with tuberous sclerosis complex (TSC) develop cortical tubers that cause severe neurological disabilities. It has been suggested that defects in neuronal differentiation and/or migration underlie the appearance of tubers. However, the precise molecular alterations remain largely unknown. Here, by combining cytological and immunohistochemical analyses of tubers from nine TSC patients (four of them diagnosed with TSC2 germline mutations), we show that alteration of microtubule biology through ROCK2 signalling contributes to TSC neuropathology. All tubers showed a larger number of binucleated neurons than expected relative to control cortex. An excess of normal and altered cytokinetic figures was also commonly observed. Analysis of centrosomal markers suggested increased microtubule nucleation capacity, which was supported by the analysis of an expression dataset from cortical tubers and control cortex, and subsequently linked to under-expression of Rho-associated coiled-coil containing kinase 2 (ROCK2). Thus, augmented microtubule nucleation capacity was observed in mouse embryonic fibroblasts and human fibroblasts deficient in the Tsc2/TSC2 gene product, tuberin. Consistent with ROCK2 under-expression, microtubule acetylation was found to be increased with tuberin deficiency; this alteration was abrogated by rapamycin treatment and mimicked by HDAC6 inhibition. Together, the results of this study support the hypothesis that loss of TSC2 expression can alter microtubule organization and dynamics, which, in turn, deregulate cell division and potentially impair neuronal differentiation.
大多数结节性硬化症(TSC)患者会出现导致严重神经功能障碍的皮质结节。有人提出,神经元分化和/或迁移缺陷是结节出现的基础。然而,确切的分子改变在很大程度上仍然未知。在这里,通过对9名TSC患者(其中4名被诊断为TSC2种系突变)的结节进行细胞学和免疫组织化学分析,我们发现通过ROCK2信号通路改变微管生物学特性会导致TSC神经病理学改变。相对于对照皮质,所有结节显示出比预期更多的双核神经元。通常还观察到过量的正常和改变的细胞动力学形态。中心体标志物分析表明微管成核能力增加,这得到了来自皮质结节和对照皮质的表达数据集分析的支持,随后与含Rho相关卷曲螺旋的激酶2(ROCK2)的表达不足相关。因此,在缺乏Tsc2/TSC2基因产物结节蛋白的小鼠胚胎成纤维细胞和人成纤维细胞中观察到微管成核能力增强。与ROCK2表达不足一致,发现结节蛋白缺乏时微管乙酰化增加;这种改变被雷帕霉素治疗消除,并被HDAC6抑制模拟。总之这项研究结果支持这样的假设,即TSC2表达缺失会改变微管组织和动力学,进而失调细胞分裂并可能损害神经元分化。