Lesma Elena, Sirchia Silvia Maria, Ancona Silvia, Carelli Stephana, Bosari Silvano, Ghelma Filippo, Montanari Emanuele, Di Giulio Anna Maria, Gorio Alfredo
Laboratory of Pharmacology, Dept. of Medicine, Surgery, and Dentistry, Via A. di Rudinì 8, 20142 Milano, Italy.
Am J Pathol. 2009 Jun;174(6):2150-9. doi: 10.2353/ajpath.2009.080799. Epub 2009 May 14.
Tuberous sclerosis complex (TSC) is an autosomal-dominant disease that is caused by mutations in either the TSC1 or TSC2 gene. Smooth muscle-like cells (ASMs) were isolated from an angiomyolipoma of a patient with TSC. These cells lacked tuberin, were labeled by both HMB45 and CD44v6 antibodies, and had constitutive S6 phosphorylation. The cells bear a germline TSC2 intron 8-exon 9 junction mutation, but DNA analysis and polymerase chain reaction amplification failed to demonstrate loss of heterozygosity. Testing for an epigenetic alteration, we detected methylation of the TSC2 promoter. Its biological relevance was confirmed by tuberin expression and a reduction in HMB45 labeling and S6 constitutive phosphorylation after exposure to the chromatin-remodeling agents, trichostatin A and 5-azacytidine. These cells were named TSC2(-/meth) ASMs. Their proliferation required epidermal growth factor in the medium as previously described for TSC2(-/-) ASMs. Blockade of epidermal growth factor with monoclonal antibodies caused the death of TSC2(-/meth) ASMs. In addition, rapamycin effectively blocked the proliferation of these cells. Our data show for the first time that methylation of the TSC2 promoter might cause a complete loss of tuberin in TSC2 cells, and that the pathogenesis of angiomyolipomas might also originate from epigenetic defects in smooth muscle cells. Additionally, the effect of chromatin-remodeling agents in these cells suggests a further avenue for the treatment of TSC as well as lymphangioleiomyomatosis.
结节性硬化症(TSC)是一种常染色体显性疾病,由TSC1或TSC2基因的突变引起。从一名TSC患者的血管平滑肌脂肪瘤中分离出平滑肌样细胞(ASMs)。这些细胞缺乏结节蛋白,被HMB45和CD44v6抗体标记,并且具有组成型S6磷酸化。这些细胞携带种系TSC2内含子8 - 外显子9连接突变,但DNA分析和聚合酶链反应扩增未能显示杂合性缺失。在检测表观遗传改变时,我们检测到TSC2启动子的甲基化。在暴露于染色质重塑剂曲古抑菌素A和5 - 氮杂胞苷后,通过结节蛋白表达、HMB45标记减少和S6组成型磷酸化减少证实了其生物学相关性。这些细胞被命名为TSC2( - /甲基化)ASMs。如先前对TSC2( - / - )ASMs所描述的那样,它们的增殖需要培养基中的表皮生长因子。用单克隆抗体阻断表皮生长因子会导致TSC2( - /甲基化)ASMs死亡。此外,雷帕霉素有效地阻断了这些细胞的增殖。我们的数据首次表明,TSC2启动子的甲基化可能导致TSC2细胞中结节蛋白完全缺失,并且血管平滑肌脂肪瘤的发病机制也可能源于平滑肌细胞中的表观遗传缺陷。此外,染色质重塑剂在这些细胞中的作用为治疗TSC以及淋巴管平滑肌瘤病提供了另一条途径。