Rahimi Ghiasi Moosa, Rahimi Elnaz, Amirkhani Zohreh, Salehi Rasoul
Department of Genetics and Molecular Biology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran.
Adv Biomed Res. 2018 Aug 31;7:125. doi: 10.4103/abr.abr_114_18. eCollection 2018.
Grape exosome-like nanovesicles (GELNs) have the advantage of inherent biocompatibility and biodegradability, the potential to be used as oral delivery vehicles. The objective of this research was to evaluate the efficiency of Syrah GELN purification and their effects on the intestinal stem cells when orally administrated to the rats.
In this experimental study, Syrah GELN isolated by differential centrifugation and sucrose gradient ultracentrifugation method, then the concentration of protein, size, and zeta potential were measured as well as nanoparticles morphology. The stability of nanoparticles was investigated in the solution that mimicked the condition encountered in the stomach and intestine. To demonstrate transfection efficiency of intestinal stem cells, real-time PCR was carried out using rat leucine-rich repeat-containing G-protein-coupled receptor 5 (Lgr5)-specific primers on cDNA derived from total RNA extracted from the upper part of the small intestine of GELN-treated rats and their controls.
The mean size, zeta potential, and concentration of nanoparticles were 205.1 nm, -12.5 mV, and 250 μg/ml, respectively. The result of stability test demonstrated that Syrah GELN were resistant to the harsh environment of the stomach. Lgr5 gene expression was increased by tenfold in GELN-treated rats compared with the controls.
As intestinal stem cells are poorly accessible by common exogenous agents , oral delivery of GELNs provides a new approach to modulate the stem cell microenvironment for intestinal remodeling. This novel and effective method would help to overcome conditions such as inflammatory bowel disease, colorectal cancer, and applicable in regenerative medicine.
葡萄外泌体样纳米囊泡(GELNs)具有固有的生物相容性和生物降解性优势,有潜力用作口服给药载体。本研究的目的是评估西拉GELN的纯化效率及其口服给予大鼠后对肠道干细胞的影响。
在本实验研究中,通过差速离心和蔗糖梯度超速离心法分离西拉GELN,然后测量蛋白质浓度、大小、zeta电位以及纳米颗粒形态。在模拟胃和肠道环境的溶液中研究纳米颗粒的稳定性。为了证明肠道干细胞的转染效率,使用大鼠富含亮氨酸重复序列的G蛋白偶联受体5(Lgr5)特异性引物对从GELN处理大鼠及其对照的小肠上部提取的总RNA衍生的cDNA进行实时PCR。
纳米颗粒平均大小、zeta电位和浓度分别为205.1 nm、-12.5 mV和250 μg/ml。稳定性测试结果表明西拉GELN对胃部恶劣环境具有抗性。与对照组相比,GELN处理大鼠的Lgr5基因表达增加了10倍。
由于普通外源性物质难以接触到肠道干细胞,口服GELNs为调节干细胞微环境以进行肠道重塑提供了一种新方法。这种新颖且有效的方法将有助于克服诸如炎症性肠病、结直肠癌等病症,并适用于再生医学。