Ni Yawen, Yu Jingyou, Xu Jin-Ping, Meng Xiao-Lin
State Key Laboratory of Virology, College of Life Sciences, Wuhan University, Wuhan, 430072, Hubei, People's Republic of China.
Endocrine. 2014 May;46(1):138-47. doi: 10.1007/s12020-013-0039-3. Epub 2013 Sep 5.
In this study, we utilized the HIV protein Tat protein transduction domain (Tat-PTD) to enhance the intestinal absorption of recombinant human growth hormone (rhGH) delivered by oral administration. Insulin-like growth factor 1 (IGF-1), the key factor in the GH signal transduction pathway, was differentially affected at the mRNA level by various concentrations of rhGH. At high rhGH concentrations (500 ng/ml), IGF-1 was downregulated, while low concentrations (5 ng/ml) caused IGF-1 upregulation. The addition of Tat-PTD had a significant facilitating effect on rhGH. Frozen tissue sections visualized with fluorescence microscopy, cultured cells visualized by confocal microscopy and flow cytometry all confirmed that rhGH fused to Tat-PTD demonstrated more intracellular fluorescent signal when compared to rhGH alone. ELISA showed that after 2 h of incubation, Tat-rhGH levels in the rat intestinal cavity were 1.38-fold higher than rhGH. These data indicated that Tat-PTD effectively improved the internalization of rhGH and enhance the signal transduction of rhGH, possibly laying a solid foundation for the novel oral administration of rhGH.
在本研究中,我们利用HIV蛋白反式激活因子蛋白转导域(Tat-PTD)来增强口服给药的重组人生长激素(rhGH)的肠道吸收。胰岛素样生长因子1(IGF-1)是生长激素信号转导途径中的关键因子,在mRNA水平上受到不同浓度rhGH的差异影响。在高浓度rhGH(500 ng/ml)时,IGF-1表达下调,而低浓度(5 ng/ml)则导致IGF-1表达上调。Tat-PTD的添加对rhGH有显著的促进作用。荧光显微镜观察的冷冻组织切片、共聚焦显微镜和流式细胞术观察的培养细胞均证实,与单独的rhGH相比,与Tat-PTD融合的rhGH表现出更多的细胞内荧光信号。ELISA显示,孵育2小时后,大鼠肠腔内Tat-rhGH水平比rhGH高1.38倍。这些数据表明,Tat-PTD有效地改善了rhGH的内化并增强了rhGH的信号转导,可能为rhGH新型口服给药奠定坚实基础。