Sánchez-Arévalo Lobo Víctor Javier, Aceves Luquero Clara Isabel, Alvarez-Vallina Luis, Tipping Alex J, Viniegra Juan Guinea, Hernández Losa Javier, Parada Cobo Carlos, Galán Moya Eva María, Gayoso Cruz Jorge, Melo Junia V, Ramón y Cajal Santiago, Sánchez-Prieto Ricardo
Immunology Department, Hospital Universitario Puerta de Hierro, 28035 Madrid, Spain.
Biochem J. 2005 Apr 1;387(Pt 1):231-8. doi: 10.1042/BJ20040927.
The chimaeric protein Bcr/Abl, the hallmark of chronic myeloid leukaemia, has been connected with several signalling pathways, such as those involving protein kinase B/Akt, JNK (c-Jun N-terminal kinase) or ERKs (extracellular-signal-regulated kinases) 1 and 2. However, no data about the p38 MAPK (mitogen-activated protein kinase) have been reported. Here, we present evidence showing that Bcr/Abl is able to modulate this signalling pathway. Transient transfection experiments indicated that overexpression of Bcr/Abl in 293T cells is able to activate p38 MAPK or induce p73 stabilization, suggesting that c-Abl and Bcr/Abl share some biological substrates. Interestingly, the control exerted by Bcr/Abl on the p38 MAPK pathway was not only mediated by the tyrosine kinase activity of Bcr/Abl, as the use of STI571 demonstrated. In fact, Bcr alone was able to induce p38 MAPK activation specifically through MKK3 (MAP kinase kinase 3). Supporting these observations, chronic myeloid leukaemia-derived K562 cells or BaF 3 cells stably transfected with Bcr/Abl showed higher levels of phosphorylated p38 MAPK compared with Bcr/Abl-negative cells. While Bcr/Abl-negative cells activated p38 MAPK in response to Ara-C (1-beta-D-arabinofuranosylcytosine), Bcr/Abl-positive cells were unable to activate p38 MAPK, suggesting that the p38 MAPK pathway is not sensitive to Abl-dependent stimuli in Bcr/Abl-positive cells. Our results demonstrate that the involvement of Bcr/Abl in the p38 MAPK pathway is a key mechanism for explaining resistance to Ara-C, and could provide a clue for new therapeutic approaches based on the use of specific Abl inhibitors.
嵌合蛋白Bcr/Abl是慢性髓性白血病的标志,与多种信号通路相关,如涉及蛋白激酶B/Akt、JNK(c-Jun氨基末端激酶)或ERK(细胞外信号调节激酶)1和2的信号通路。然而,关于p38丝裂原活化蛋白激酶(p38 MAPK)的数据尚未见报道。在此,我们提供证据表明Bcr/Abl能够调节这一信号通路。瞬时转染实验表明,在293T细胞中过表达Bcr/Abl能够激活p38 MAPK或诱导p73稳定,这表明c-Abl和Bcr/Abl共享一些生物学底物。有趣的是,如使用STI571所证明的,Bcr/Abl对p38 MAPK通路的调控不仅由Bcr/Abl的酪氨酸激酶活性介导。事实上,单独的Bcr能够通过MKK3(丝裂原活化蛋白激酶激酶3)特异性诱导p38 MAPK活化。支持这些观察结果的是,稳定转染Bcr/Abl的慢性髓性白血病来源的K562细胞或BaF 3细胞与Bcr/Abl阴性细胞相比,显示出更高水平的磷酸化p38 MAPK。虽然Bcr/Abl阴性细胞在Ara-C(1-β-D-阿拉伯呋喃糖基胞嘧啶)刺激下激活p38 MAPK,但Bcr/Abl阳性细胞无法激活p38 MAPK,这表明p38 MAPK通路对Bcr/Abl阳性细胞中依赖Abl的刺激不敏感。我们的结果表明,Bcr/Abl参与p38 MAPK通路是解释对Ara-C耐药的关键机制,并可能为基于使用特异性Abl抑制剂的新治疗方法提供线索。