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1.
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  • •Matrisome content significantly changes with development and perlecan knockdown.
  • •Chondrocytes respond to perlecan deficiency by increasing bulk matrisome secretion.
  • •Decreased stiffness may be explained by atypical glycosaminoglycan deposition.
  • •Elevated COL10A1 expression and chondrocyte hypertrophy indicate early ossification.
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2.
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  • •Proteomes measured from human heart biopsies collected in-vivo covers >7000 cardiac proteins and highlight hundreds of chamber-specific molecular signatures that meaningfully reflect the specialized functions of the respective chambers.
  • •Protein quantification from freshly collected biopsies is preferential to necropsy samples because of unspecific post-mortem protein degradation in the latter.
  • •Increased abundances of proteins associated with sustained atrial fibrillation are not a sufficient condition to generate the disease state.
  • •Protein abundance differences between atria and ventricle primarily originate at the level of gene regulation and reflect a functional need.
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3.
摘要细胞外基质(extracellular matrix,ECM)重塑是癌细胞迁移的关键步骤.本研究基于乳腺癌组织的基因表达谱数据,采用系统生物学方法推测乳腺癌转移中Runx2对细胞外基质重塑的调节机制.采用相关性分析程序分析49例乳腺原发癌和15例淋巴结转移癌组织的基因表达谱数据,筛选与Runx2呈相关性表达的基因,结果得到与ECM重塑相关的候选基因52个,包括ECM成分11个,ECM降解酶及其抑制剂8个,细胞信号分子33个.利用转录调节因子结合序列数据库搜索候选基因启动子区的Runx2结合模序,筛选其中Runx2转录调控的ECM重塑相关基因,并判断可能调节Runx2的上游信号分子;文献检索实验证实的与Runx2有相互调节关系的基因,并基于Runx2上游调控信号分子和下游转录调节基因的分析,构建得到以Runx2为中心的ECM重塑的生物学调控网络.WNT和TGF/BMPs是启动Runx2表达的主要信号通路,Runx2通过转录调节ECM组分、ECM降解酶及其抑制剂和信号分子调节ECM重塑,促进癌细胞完成转移的生物学过程.  相似文献   

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