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骨髓增生异常综合征患者外周血单个核细胞蛋白质组变化

Peripheral blood mononuclear cell proteome changes in patients with myelodysplastic syndrome.

作者信息

Pecankova Klara, Majek Pavel, Cermak Jaroslav, Dyr Jan E

机构信息

Institute of Hematology and Blood Transfusion, U Nemocnice 1, 128 20 Prague 2, Czech Republic.

出版信息

Biomed Res Int. 2015;2015:872983. doi: 10.1155/2015/872983. Epub 2015 Apr 16.

Abstract

Our aim was to search for proteome changes in peripheral blood mononuclear cells (PBMCs) of MDS patients with refractory cytopenia with multilineage dysplasia. PBMCs were isolated from a total of 12 blood samples using a Histopaque-1077 solution. The proteins were fractioned, separated by 2D SDS-PAGE (pI 4-7), and double-stained. The proteomes were compared and statistically processed with Progenesis SameSpots; then proteins were identified by nano-LC-MS/MS. Protein functional association and expression profiles were analyzed using the EnrichNet application and Progenesis SameSpots hierarchical clustering software, respectively. By comparing the cytosolic, membrane, and nuclear fractions of the two groups, 178 significantly (P < 0.05, ANOVA) differing spots were found, corresponding to 139 unique proteins. Data mining of the Reactome and KEGG databases using EnrichNet highlighted the possible involvement of the identified protein alterations in apoptosis, proteasome protein degradation, heat shock protein action, and signal transduction. Western blot analysis revealed underexpression of vinculin and advanced fragmentation of fermitin-3 in MDS patients. To the best of our knowledge, this is the first time that proteome changes have been identified in the mononuclear cells of MDS patients. Vinculin and fermitin-3, the proteins involved in cell adhesion and integrin signaling, have been shown to be dysregulated in MDS.

摘要

我们的目的是寻找伴有多系发育异常的难治性血细胞减少的骨髓增生异常综合征(MDS)患者外周血单个核细胞(PBMCs)中的蛋白质组变化。使用Histopaque - 1077溶液从总共12份血液样本中分离出PBMCs。对蛋白质进行分级分离,通过二维SDS - PAGE(pH值4 - 7)进行分离并进行双重染色。使用Progenesis SameSpots软件对蛋白质组进行比较和统计处理;然后通过纳升液相色谱 - 串联质谱(nano - LC - MS/MS)鉴定蛋白质。分别使用EnrichNet应用程序和Progenesis SameSpots层次聚类软件分析蛋白质功能关联和表达谱。通过比较两组的胞质、膜和核部分,发现了178个差异显著(P < 0.05,方差分析)的斑点,对应139种独特蛋白质。使用EnrichNet对Reactome和KEGG数据库进行数据挖掘,突出了已鉴定的蛋白质改变可能参与细胞凋亡、蛋白酶体蛋白降解、热休克蛋白作用和信号转导。蛋白质印迹分析显示MDS患者中纽蛋白表达不足以及fermitin - 3高度碎片化。据我们所知,这是首次在MDS患者的单核细胞中鉴定出蛋白质组变化。纽蛋白和fermitin - 3这两种参与细胞黏附和整合素信号传导的蛋白质,在MDS中已被证明存在失调。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/674c/4415457/0d33557a9813/BMRI2015-872983.001.jpg

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