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Comparative serum proteome expression of osteonecrosis of the femoral head in adults.

机译:成人股骨头坏死的血清蛋白质组比较表达。

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Osteonecrosis of the femoral head (ONFH) is a skeletal disorder characterized by ischemic deterioration, bone marrow edema and eventually femoral head collapse. The systemic regulation of ONFH in adult patients has not been examined. Serum proteomic is an innovative tool that potentially detects simultaneous expressions of serum proteins in pathological contexts. We compared the serum proteome profiles of 11 adult patients with ONFH (3 females and 8 males) and 11 healthy volunteers (3 females and 8 males). The proteins in the aliquots of sera were subjected to isoelectric focusing, two-dimensional gel electrophoresis and silver staining. The protein spots were matched and quantified using an imaging analysis system. The differentially expressed protein spots were subjected to in-gel trypsin digestion. The peptide mass fingerprints were identified by matrix-assisted laser desorption ionization time-of-flight mass spectrometry (MALDI-TOF/TOF) and a bioinformation search. We found that ONFH patients showed significantly higher abundances of kininogen 1 variant, complement factor C3 precursor, and complement factor H and lower levels of antithrombin III chain B, apolipoprotein A--IV precursor, and gelsolin isoform alpha precursor. These proteins of interest were reported to modulate thrombotic/fibrinolytic reactions, oxidative stress, vessel injury, tissue necrosis or cell apoptosis in several tissue types under pathological contexts. Taken together, the occurrence of ONFH was associated with various serum protein expressions. Our high--throughput serum proteomic findings indicated that multiple pathological reactions presumably occurred in ONFH.
机译:股骨头坏死(ONFH)是一种骨骼疾病,其特征在于缺血性恶化,骨髓水肿和最终股骨头塌陷。成年患者ONFH的全身调节尚未检查。血清蛋白质组学是一种创新工具,可以在病理情况下检测血清蛋白的同时表达。我们比较了11例成人ONFH患者(3名女性和8名男性)和11名健康志愿者(3名女性和8名男性)的血清蛋白质组学特征。将等份血清中的蛋白质进行等电聚焦,二维凝胶电泳和银染。使用成像分析系统对蛋白质斑点进行匹配和定量。对差异表达的蛋白斑点进行凝胶内胰蛋白酶消化。通过基质辅助激光解吸电离飞行时间质谱(MALDI-TOF / TOF)和生物信息搜索来鉴定肽质量指纹。我们发现ONFH患者显示激肽原1变体,补体因子C3前体和补体因子H的丰度显着较高,抗凝血酶III链B,载脂蛋白A-IV的前体和凝溶胶蛋白同工型的α的前体水平较低。据报道,这些感兴趣的蛋白质在病理情况下可调节多种组织类型中的血栓/纤维蛋白溶解反应,氧化应激,血管损伤,组织坏死或细胞凋亡。两者合计,ONFH的发生与各种血清蛋白表达有关。我们的高通量血清蛋白质组学发现表明,在ONFH中可能发生了多种病理反应。

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