Key Laboratory of Molecular Developmental Biology, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing 100080, China.
Biomaterials. 2011 Apr;32(12):3244-52. doi: 10.1016/j.biomaterials.2011.01.039.
Brain derived neurotrophic factor (BDNF) has been shown to ameliorate recovery after intracerebral hemorrhage (ICH). The injured brain tissue after ICH is surrounded by hematoma formed from hemorrhage. Fibrin is abundant in hematoma, which could be a binding target for BDNF. In this work, we have fused a fibrin-binding domain (FBD) to BDNF (FBD-BDNF), and results demonstrate that FBD-BDNF has specific binding ability to fibrin and is retained in hematoma. Using the rat ICH model induced by bacterial collagenase, injected FBD-BDNF has been concentrated and retained at the hematoma. FBD has facilitated BDNF to exert targeting neuroprotective effect to the injured brain tissue around the hematoma after ICH. FBD-BDNF has significantly reduced the hemotoma volume, reduced tissue loss, promoted neural regeneration, and improved the rat behavioral performance.
脑源性神经营养因子(BDNF)已被证明可以改善脑出血(ICH)后的恢复。ICH 后受损的脑组织被血肿形成的血液所包围。纤维蛋白在血肿中含量丰富,可能是 BDNF 的结合靶点。在这项工作中,我们将纤维蛋白结合结构域(FBD)融合到 BDNF 中(FBD-BDNF),结果表明 FBD-BDNF 对纤维蛋白具有特异性结合能力,并保留在血肿中。使用细菌胶原酶诱导的大鼠 ICH 模型,注射 FBD-BDNF 可被浓缩并保留在血肿中。FBD 促进了 BDNF 对 ICH 后血肿周围受损脑组织发挥靶向神经保护作用。FBD-BDNF 显著减少了血肿体积,减少了组织损失,促进了神经再生,并改善了大鼠的行为表现。