The Children's Cancer Hospital, The University of Texas M. D. Anderson Cancer Center, Houston, TX, USA.
Blood. 2011 Jan 13;117(2):719-26. doi: 10.1182/blood-2010-05-284869. Epub 2010 Oct 13.
Delta-like ligand 4 (DLL4) is essential for the formation of mature vasculature. However, the role of DLL4-Notch signaling in pericyte/vascular smooth muscle cell (vSMC) development is poorly understood. We sought to determine whether DLL4-Notch signaling is involved in pericyte/vSMC formation in vitro and during vasculogenesis in vivo using 2 Ewing sarcoma mouse models. Inhibition of DLL4 with the antibody YW152F inhibited pericyte/vSMC marker expression by bone marrow (BM) cells in vitro. Conversely, transfection of 10T1/2 cells with the active domains of Notch receptors led to increased expression of pericyte/vSMC markers. Furthermore, the blood vessels of Ewing sarcoma tumors from mice treated with YW152F had reduced numbers of BM-derived pericytes/vSMCs, fewer open lumens, and were less functional than the vessels in tumors of control-treated mice. Tumor growth was also inhibited. These data demonstrate a specific role for DLL4 in the formation of BM-derived pericytes/vSMCs and indicate that DLL4 may be a novel therapeutic target for the inhibition of vasculogenesis.
Delta-like ligand 4 (DLL4) 对于成熟血管的形成至关重要。然而,DLL4-Notch 信号在周细胞/血管平滑肌细胞 (vSMC) 发育中的作用尚不清楚。我们试图使用两种尤因肉瘤小鼠模型来确定 DLL4-Notch 信号是否参与体外周细胞/vSMC 形成和体内血管发生。用抗体 YW152F 抑制 DLL4 可抑制骨髓 (BM) 细胞体外的周细胞/vSMC 标志物表达。相反,转染 Notch 受体的活性结构域可导致周细胞/vSMC 标志物表达增加。此外,用 YW152F 治疗的小鼠的尤因肉瘤肿瘤中的血管中 BM 来源的周细胞/vSMC 数量减少,管腔开放较少,功能不如对照治疗小鼠的肿瘤中的血管。肿瘤生长也受到抑制。这些数据表明 DLL4 在 BM 来源的周细胞/vSMC 的形成中具有特定作用,并表明 DLL4 可能是抑制血管发生的新型治疗靶标。