Tang Jian, Niu Jing-Wen, Xu Dong-Hui, Li Zhi-Xing, Li Qi-Fu, Chen Jin-An
The Key Laboratory of Chinese Ministry of Education for Cell Biology and Tumor Cell Engineering, School of Life Sciences, Xiamen University, Xiamen, Fujian Province, China.
World J Gastroenterol. 2007 May 28;13(20):2791-7. doi: 10.3748/wjg.v13.i20.2791.
To investigate the association between the configurational and compositional changes of nuclear matrix and the differentiation of carcinoma cells.
Cells cultured with or without 5 x 10(-3) mmol/L of hexamethylene bisacetamide (HMBA) on Nickel grids were treated by selective extraction and prepared for whole mount observation under electron microscopy. The samples were examined under transmission electron microscope. Nuclear matrix proteins were selectively extracted and subjected to subcellular proteomics study. The protein expression patterns were analyzed by PDQuest software. Spots of differentially expressed nuclear matrix proteins were excised and subjected to in situ digestion with trypsin. The peptides were analyzed by matrix-assisted laser-desorption/ionization time of flight mass spectrometry (MALDI-TOF-MS). Data were submitted for database searching using Mascot tool (www.matrixscience.com).
The nuclear matrix (NM) and intermediate filament (IF) in SMMC-7721 hepatocarcinoma cells were found relatively sparse and arranged irregularly. The nuclear lamina was non-uniform, and two kinds of filaments were not tightly connected. After induction for differentiation by HMBA, the NM-IF filaments were concentrated and distributed uniformly. The heterogeneous population of filaments, including highly branched ultrathin filaments could also be seen in the regular meshwork. The connection between the two kinds of filaments and the relatively thin, condensed and sharply demarcated lamina composed of intermediate-sized filaments was relatively fastened. Meanwhile, 21 NM proteins changed remarkably during SMMC-7721 cell differentiation. Four proteins, i.e. mutant Pyst1, hypothetical protein, nucleophosmin 1, and LBP were downregulated, whereas four other proteins, eIF6, p44 subunit, beta-tubulin, and SIN3B were upregulated with the last one, SR2/ASF found only in the differentiated SMMC-7721 cells.
The induced differentiation of SMMC-7721 cells by HMBA is accompanied by the configurational changes of nuclear matrix-intermediate filament (NM-IF) system and the compositional changes of nuclear matrix protein expression. These changes may be important morphological or functional indications of the cancer cell reversion.
研究核基质的结构和组成变化与癌细胞分化之间的关联。
将在镍网上培养的细胞分为添加或不添加5×10⁻³ mmol/L六亚甲基双乙酰胺(HMBA)两组,经选择性抽提处理后,制备用于电子显微镜整装观察的样本。在透射电子显微镜下对样本进行检查。选择性抽提核基质蛋白并进行亚细胞蛋白质组学研究。用PDQuest软件分析蛋白质表达模式。切除差异表达的核基质蛋白斑点并用胰蛋白酶进行原位消化。通过基质辅助激光解吸/电离飞行时间质谱(MALDI-TOF-MS)分析肽段。使用Mascot工具(www.matrixscience.com)将数据提交至数据库进行检索。
发现SMMC-7721肝癌细胞中的核基质(NM)和中间丝(IF)相对稀疏且排列不规则。核纤层不均匀,两种丝连接不紧密。经HMBA诱导分化后,NM-IF丝浓缩且分布均匀。在规则的网络结构中还可见到包括高度分支的超薄丝在内的异质丝群体。两种丝之间的连接以及由中等大小丝组成的相对较薄、浓缩且界限清晰的核纤层连接相对紧密。同时,21种核基质蛋白在SMMC-7721细胞分化过程中发生显著变化。四种蛋白,即突变型Pyst1、假定蛋白、核磷蛋白1和LBP表达下调,而另外四种蛋白,即eIF6、p44亚基、β-微管蛋白和SIN3B表达上调,其中最后一种蛋白SR2/ASF仅在分化的SMMC-7721细胞中发现。
HMBA诱导SMMC-7721细胞分化伴随着核基质-中间丝(NM-IF)系统的结构变化以及核基质蛋白表达的组成变化。这些变化可能是癌细胞逆转的重要形态学或功能学指标。