Experimental Clinical Chemistry, Department of Laboratory Medicine, Lund University, Wallenberg Laboratory, Skåne University Hospital, 20502 Malmö, Sweden.
Mol Oncol. 2013 Jun;7(3):693-703. doi: 10.1016/j.molonc.2013.02.020. Epub 2013 Mar 19.
The suppressor of cytokine signaling 2 (SOCS2) is a member of the SOCS family of E3 ubiquitin ligases. SOCS2 is known to regulate signal transduction by cytokine receptors and receptor tyrosine kinases. The receptor tyrosine kinase FLT3 is of importance for proliferation, survival and differentiation of hematopoietic cells and is frequently mutated in acute myeloid leukemia. We observed that SOCS2 associates with activated FLT3 through phosphotyrosine residues 589 and 919, and co-localizes with FLT3 in the cell membrane. SOCS2 increases FLT3 ubiquitination and accelerates receptor degradation in proteasomes. SOCS2 negatively regulates FLT3 signaling by blocking activation of Erk 1/2 and STAT5. Furthermore, SOCS2 expression leads to a decrease in FLT3-ITD-mediated cell proliferation and colony formation. Thus, we suggest that SOCS2 associates with activated FLT3 and negatively regulates the FLT3 signaling pathways.
细胞因子信号转导抑制因子 2(SOCS2)是 E3 泛素连接酶 SOCS 家族的一员。SOCS2 已知可调节细胞因子受体和受体酪氨酸激酶的信号转导。受体酪氨酸激酶 FLT3 对造血细胞的增殖、存活和分化很重要,并且在急性髓系白血病中经常发生突变。我们观察到 SOCS2 通过磷酸酪氨酸残基 589 和 919 与激活的 FLT3 结合,并与 FLT3 在细胞膜中共定位。SOCS2 增加 FLT3 的泛素化并加速蛋白酶体中的受体降解。SOCS2 通过阻断 Erk 1/2 和 STAT5 的激活来负调控 FLT3 信号。此外,SOCS2 的表达导致 FLT3-ITD 介导的细胞增殖和集落形成减少。因此,我们认为 SOCS2 与激活的 FLT3 结合并负调控 FLT3 信号通路。