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Activated human platelets release connective tissue growth factor.

机译:活化的人血小板释放结缔组织生长因子。

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摘要

Connective tissue growth factor (CTGF) is overexpressed in wound healing, fibrosis and advanced atherosclerotic lesions. Platelets adhere to CTGF, suggesting that this protein may be involved in the formation of platelet-rich thrombi at the sites of tissue injury or atherosclerotic plaque rupture. Since platelets contain a wide array of biologically active proteins, we investigated the presence, localization and release of CTGF from these cells. For this purpose, human platelets from healthy donors were washed and stimulated with thrombin or ADP. Following incubation, proteins from unstimulated and stimulated cell lysates and the supernatants were analysed by Western blotting. The experiments showed that unstimulated platelets contain considerable amounts of CTGF, whereas no CTGF was detectable in platelet-poor plasma. To elucidate the origin of CTGF in platelets, we performed immunohistochemical analysis of human bone marrow sections. The analysis showed that although CTGF protein is widely expressed in bone marrow cells, it is not expressed by platelet-producing megakaryocytes, suggesting that CTGF presence in platelets is a result of endocytosis from extracellular environment in bone marrow. Agonist-stimulation of platelets resulted in a significant release of CTGF from the storage granules, with thrombin at 0.1 U/mL being a more potent activator than ADP at 20 micro mol/L.The agonist-dependent CTGF secretion was significantly inhibited by aspirin. In conclusion, CTGF is stored in normal human platelets, and can be released upon platelet activation. Aspirin treatment prevents CTGF release, suggesting that clinical benefits of this drug may involve the inhibition of CTGF secretion.
机译:结缔组织生长因子(CTGF)在伤口愈合,纤维化和晚期动脉粥样硬化病变中过表达。血小板粘附于CTGF,表明该蛋白可能与组织损伤或动脉粥样硬化斑块破裂处富含血小板的血栓形成有关。由于血小板包含多种生物活性蛋白,因此我们研究了CTGF从这些细胞中的存在,定位和释放。为此,将来自健康供体的人血小板洗涤并用凝血酶或ADP刺激。孵育后,通过蛋白质印迹分析未刺激和刺激的细胞裂解液和上清液中的蛋白质。实验表明,未刺激的血小板含有大量的CTGF,而在贫血小板的血浆中未检测到CTGF。为了阐明CTGF在血小板中的起源,我们对人体骨髓切片进行了免疫组织化学分析。分析显示,尽管CTGF蛋白在骨髓细胞中广泛表达,但血小板生成的巨核细胞却不表达CTGF蛋白,这表明血小板中CTGF的存在是骨髓细胞外环境内吞作用的结果。激动剂刺激血小板导致CTGF从储存颗粒中大量释放,0.1 U / mL的凝血酶比20μmol/ L的ADP更有效。活化剂依赖性CTGF的分泌被阿司匹林抑制。总之,CTGF被储存在正常的人类血小板中,并且可以在血小板活化后释放。阿司匹林治疗可防止CTGF释放,表明该药的临床益处可能涉及抑制CTGF分泌。

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