Activated tyrosine kinase c‐Src‐responsive artificial gene carrier: in vitro and in vivo evaluation

Author:

Terada Keiko1,Asai Daisuke2ORCID,Kang Jeong‐Hun3ORCID,Mori Takeshi14,Katayama Yoshiki14567ORCID

Affiliation:

1. Graduate School of System Life Sciences Kyushu University 744 Moto-oka, Nishi-ku Fukuoka 819-0395 Japan

2. Laboratory of Microbiology Showa Pharmaceutical University 3-3165 Higashi-Tamagawagakuen Machida Tokyo 194-8543 Japan

3. National Cerebral and Cardiovascular Center Research Institute 6-1 Shinmachi, Kishibe Suita Osaka 564-8565 Japan

4. Department of Applied Chemistry Faculty of Engineering Kyushu University 744 Moto-oka, Nishi-ku Fukuoka 819-0395 Japan

5. Center for Future Chemistry Kyushu University 744 Moto-oka, Nishi-ku Fukuoka 819-0395 Japan

6. International Research Center for Molecular Systems Kyushu University

7. Department of Biomedical Engineering Chung Yuan Christian University

Abstract

AbstractThe proto‐oncogene c‐Src is a protein‐tyrosine kinase that is associated with increased risk of acute and chronic kidney diseases, cardiovascular diseases, neurological diseases, and cancers. The purpose of this study was to develop a gene delivery carrier responding to activated c‐Src and to evaluate its efficacy in vitro and in vivo. The polymeric gene carrier consists of a neutral main chain bearing a peptide substrate of c‐Src or negative control peptide. Complexes of the polymer containing c‐Src‐targeting peptides and DNA were phosphorylated in the presence of c‐Src, resulting in release of the DNA. Green fluorescent protein (GFP) expression was observed after microinjection of complexes of polymer containing c‐Src‐targeting peptides and GFP‐encoding DNA into A431 cells at the nitrogen/phosphate (N/P) ratio of 1.0. GFP was not expressed in cells microinjected with negative control polymer/DNA complex. Direct injection of complexes of polymer containing c‐Src‐targeting peptides and luciferase‐encoding DNA at N/P ratios of 1.0 and 2.0 into tumor‐bearing mice resulted in luciferase expression in A431 tumors but not in normal skin tissues. No luciferase expression was observed in A431 tumors or skin tissues after injection of control polymer/DNA complex. These results indicate that our gene delivery carrier enables activated c‐Src‐specific gene expression.

Publisher

Wiley

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3