4.8 Article

Ultrasound-Targeted Microbubble Destruction Mediates Gene Transfection for Beta-Cell Regeneration and Glucose Regulation

期刊

SMALL
卷 17, 期 31, 页码 -

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/smll.202008177

关键词

cell metabolism; diabetes; gene transfection; microbubbles; ultrasound

资金

  1. National Key RAMP
  2. D Program of China [2018YFC0115900]
  3. National Natural Science Foundation of China [82030048, 81527803, 81901871, 82001818]
  4. Zhejiang Science and Technology Project [2019C03077, Y16H180019]
  5. Natural Science Foundation of Zhejiang Province [Y16H180019, LQ21H180007]
  6. Natural Science Foundation of Guangdong Province [2016A030311054]
  7. Shanghai Rising-Star Program [19QA1404800]
  8. Innovation Research Plan by the Shanghai Municipal Education Commission [ZXWF082101]
  9. Second Affiliated Hospital of Zhejiang University [2019002]

向作者/读者索取更多资源

The study demonstrated successful gene delivery of GLP-1 in macaques using UTMD, leading to enhanced GLP-1 expression and improvement in pancreatic beta cell regeneration and plasma glucose regulation. This approach shows promising alternatives for treating type 2 diabetes.
Ultrasound-targeted microbubble destruction (UTMD) mediates gene transfection with high biosafety and thus has been promising toward treatment of type 1 diabetes. However, the potential application of UTMD in type 2 diabetes (T2D) is still limited, due to the lack of systematic design and dynamic monitoring. Herein, an efficient gene delivery system is constructed by plasmid deoxyribonucleic acid (DNA) encoding glucagon-like peptide 1 (GLP-1) in ultrasound-induced microbubbles, toward treatment of T2D in macaque. The as designed UTMD afforded enhancement of cell membrane penetration and GLP-1 expression in macaque, which is characterized by ultrasound-guided biopsy to monitor the dynamic process of islet cells for 6 months. Also, improvement of pancreatic beta cell regeneration, and regulation of plasma glucose in macaque with T2D is achieved. The approach would serve as promising alternatives for the treatment of T2D.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.8
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据