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源自背根神经节的成纤维细胞生长因子(FGF)和骨形态发生蛋白(BMP)调节墨西哥钝口螈肢体再生中的芽基诱导。

FGF and BMP derived from dorsal root ganglia regulate blastema induction in limb regeneration in Ambystoma mexicanum.

作者信息

Satoh Akira, Makanae Aki, Nishimoto Yurie, Mitogawa Kazumasa

机构信息

Okayama University, Research Core for Interdisciplinary Sciences (RCIS), 3-1-1 Tsushimanaka, Kita-ku, Okayama 700-8530, Japan.

Okayama University, Research Core for Interdisciplinary Sciences (RCIS), 3-1-1 Tsushimanaka, Kita-ku, Okayama 700-8530, Japan.

出版信息

Dev Biol. 2016 Sep 1;417(1):114-25. doi: 10.1016/j.ydbio.2016.07.005. Epub 2016 Jul 16.

Abstract

Urodele amphibians have a remarkable organ regeneration ability that is regulated by neural inputs. The identification of these neural inputs has been a challenge. Recently, Fibroblast growth factor (Fgf) and Bone morphogenic protein (Bmp) were shown to substitute for nerve functions in limb and tail regeneration in urodele amphibians. However, direct evidence of Fgf and Bmp being secreted from nerve endings and regulating regeneration has not yet been shown. Thus, it remained uncertain whether they were the nerve factors responsible for successful limb regeneration. To gather experimental evidence, the technical difficulties involved in the usage of axolotls had to be overcome. We achieved this by modifying the electroporation method. When Fgf8-AcGFP or Bmp7-AcGFP was electroporated into the axolotl dorsal root ganglia (DRG), GFP signals were detectable in the regenerating limb region. This suggested that Fgf8 and Bmp7 synthesized in neural cells in the DRG were delivered to the limbs through the long axons. Further knockdown experiments with double-stranded RNA interference resulted in impaired limb regeneration ability. These results strongly suggest that Fgf and Bmp are the major neural inputs that control the organ regeneration ability.

摘要

有尾两栖动物具有由神经输入调节的显著器官再生能力。识别这些神经输入一直是一项挑战。最近,成纤维细胞生长因子(Fgf)和骨形态发生蛋白(Bmp)被证明可在有尾两栖动物的肢体和尾巴再生中替代神经功能。然而,Fgf和Bmp从神经末梢分泌并调节再生的直接证据尚未得到证实。因此,它们是否是导致肢体成功再生的神经因子仍不确定。为了收集实验证据,必须克服使用美西螈所涉及的技术难题。我们通过改进电穿孔方法实现了这一点。当将Fgf8-AcGFP或Bmp7-AcGFP电穿孔到美西螈背根神经节(DRG)中时,在再生肢体区域可检测到绿色荧光蛋白(GFP)信号。这表明在DRG神经细胞中合成的Fgf8和Bmp7通过长轴突被输送到肢体。进一步使用双链RNA干扰进行的敲低实验导致肢体再生能力受损。这些结果有力地表明,Fgf和Bmp是控制器官再生能力的主要神经输入。

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