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Potentiated activation of VLA-4 and VLA-5 accelerates proplatelet-like formation

机译:VLA-4和VLA-5的增强激活可加速血小板样形成

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Fibronectin (FN) plays important roles in the proliferation, differentiation, and maintenance of megakaryocytic-lineage cells through FN receptors. However, substantial role of FN receptors and their functional assignment in proplatelet-like formation (PPF) of megakaryocytes are not yet fully understood. Herein, we investigated the effects of FN receptors on PPF using the CHRF-288 human megakaryoblastic cell line, which expresses VLA-4 and VLA-5 as FN receptors. FN and phorbol 12-myristate 13-acetate (PMA) were essential for inducing PPF in CHRF-288 cells. Blocking experiments using anti-β1-integrin monoclonal antibodies indicated that the adhesive interaction with FN via VLA-4 and VLA-5 were required for PPF. PPF induced by FN plus PMA was accelerated when CHRF-288 cells were enforced adhering to FN by TNIIIA2, a peptide derived from tenascin-C, which we recently found to induce β1-integrin activation. Adhesion to FN enhanced PMA-stimulated activation of extracellular signal-regulated protein kinase 1 (ERK1)/2 and enforced adhesion to FN via VLA-4 and VLA-5 by TNIIIA2-accelerated activation of ERK1/2 with FN plus PMA. However, c-Jun amino-terminal kinase 1 (JNK1), p38, and phosphoinositide-3 kinase (PI3K)/Akt were not stimulated by FN plus PMA, even with TNIIIA2. Thus, the enhanced activation of ERK1/2 by FN, PMA plus TNIIIA2 was responsible for acceleration of PPF with FN plus PMA.
机译:纤连蛋白(FN)通过FN受体在巨核细胞系细胞的增殖,分化和维持中起着重要作用。但是,尚未完全了解FN受体的实质作用及其在巨核细胞的血小板样形成(PPF)中的功能分配。本文中,我们使用表达VLA-4和VLA-5作为FN受体的CHRF-288人巨核细胞系研究了FN受体对PPF的影响。 FN和佛波醇12-肉豆蔻酸酯13-醋酸酯(PMA)对于诱导CHRF-288细胞中的PPF至关重要。使用抗β1-整合素单克隆抗体的阻断实验表明,PPF需要通过VLA-4和VLA-5与FN进行胶粘剂相互作用。当TNIIIA2(一种来自腱生蛋白-C的肽)促使CHRF-288细胞粘附于FN时,由FN加PMA诱导的PPF得以加速。对FN的粘附增强了PMA刺激的细胞外信号调节蛋白激酶1(ERK1)/ 2的激活,并通过TNIIIA2通过FN加PMA加速ERK1 / 2的激活,通过VLA-4和VLA-5增强了对FN的粘附。但是,FN加PMA甚至不会用TNIIIA2刺激c-Jun氨基末端激酶1(JNK1),p38和磷酸肌醇3激酶(PI3K)/ Akt。因此,FN,PMA和TNIIIA2对ERK1 / 2的增强激活是FN和PMA加速PPF的原因。

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