Preferential delivery of lipid-ligand conjugated DNA/RNA heteroduplex oligonucleotide to ischemic brain in hyperacute stage

共轭体系 配体(生物化学) DNA 寡核苷酸 异源双工 阶段(地层学) 受体 生物 基因 核糖核酸 化学 分子生物学 生物化学 古生物学 有机化学 聚合物
作者
Fuying Li,Keiko Ichinose,Satoru Ishibashi,Satoshi Yamamoto,Eri Iwasawa,Motohiro Suzuki,Kie Yoshida-Tanaka,Koshiro Yoshioka,Tetsuya Nagata,Hideki Hirabayashi,Kaoru Mogushi,Takanori Yokota
出处
期刊:Molecular Therapy [Elsevier BV]
卷期号:31 (4): 1106-1122
标识
DOI:10.1016/j.ymthe.2023.01.016
摘要

Antisense oligonucleotide (ASO) is a major tool used for silencing pathogenic genes. For stroke in the hyperacute stage, however, the ability of ASO to regulate genes is limited by its poor delivery to the ischemic brain owing to sudden occlusion of the supplying artery. Here we show that, in a mouse model of permanent ischemic stroke, lipid-ligand conjugated DNA/RNA heteroduplex oligonucleotide (lipid-HDO) was unexpectedly delivered 9.6 times more efficiently to the ischemic area of the brain than to the contralateral non-ischemic brain and achieved robust gene knockdown and change of stroke phenotype, despite a 90% decrease in cerebral blood flow in the 3 h after occlusion. This delivery to neurons was mediated via receptor-mediated transcytosis by lipoprotein receptors in brain endothelial cells, the expression of which was significantly upregulated after ischemia. This study provides proof-of-concept that lipid-HDO is a promising gene-silencing technology for stroke treatment in the hyperacute stage. Antisense oligonucleotide (ASO) is a major tool used for silencing pathogenic genes. For stroke in the hyperacute stage, however, the ability of ASO to regulate genes is limited by its poor delivery to the ischemic brain owing to sudden occlusion of the supplying artery. Here we show that, in a mouse model of permanent ischemic stroke, lipid-ligand conjugated DNA/RNA heteroduplex oligonucleotide (lipid-HDO) was unexpectedly delivered 9.6 times more efficiently to the ischemic area of the brain than to the contralateral non-ischemic brain and achieved robust gene knockdown and change of stroke phenotype, despite a 90% decrease in cerebral blood flow in the 3 h after occlusion. This delivery to neurons was mediated via receptor-mediated transcytosis by lipoprotein receptors in brain endothelial cells, the expression of which was significantly upregulated after ischemia. This study provides proof-of-concept that lipid-HDO is a promising gene-silencing technology for stroke treatment in the hyperacute stage.

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
论文多多完成签到,获得积分10
3秒前
包容笑珊发布了新的文献求助10
9秒前
zyc完成签到 ,获得积分10
11秒前
神可馨完成签到 ,获得积分10
11秒前
hefang完成签到,获得积分10
14秒前
pluto应助小字采纳,获得10
14秒前
粗犷的月饼完成签到 ,获得积分10
15秒前
我想毕业完成签到,获得积分10
16秒前
棈棦完成签到 ,获得积分10
19秒前
乐乐呀完成签到 ,获得积分10
20秒前
suliang完成签到,获得积分10
21秒前
22秒前
Licifer完成签到,获得积分10
23秒前
23秒前
印第安老斑鸠应助Xiaoxiao采纳,获得10
24秒前
坦率的丹云完成签到,获得积分10
26秒前
SCI完成签到 ,获得积分10
28秒前
云深不知处完成签到,获得积分10
28秒前
sirhai发布了新的文献求助10
29秒前
Lsy完成签到,获得积分10
30秒前
Orange应助Hodlumm采纳,获得10
32秒前
32秒前
33秒前
ccccchen完成签到,获得积分10
34秒前
wy0409完成签到,获得积分10
36秒前
壮观的菠萝完成签到,获得积分10
36秒前
Selonfer完成签到,获得积分10
38秒前
小马甲应助ZHANG采纳,获得10
39秒前
sdfwsdfsd完成签到,获得积分10
39秒前
蓝天发布了新的文献求助10
39秒前
xx发布了新的文献求助10
40秒前
今晚打老虎完成签到,获得积分10
41秒前
小鬼完成签到 ,获得积分10
41秒前
liujunhong完成签到,获得积分10
44秒前
pluto应助小字采纳,获得10
44秒前
854fycchjh完成签到,获得积分10
45秒前
爱就跟我走完成签到,获得积分10
45秒前
45秒前
田様应助LZ采纳,获得10
46秒前
久伴久爱完成签到 ,获得积分10
46秒前
高分求助中
液晶指向矢仿真分析数据集 8888
Invited Discussant 63O and 64O 1000
Ideology and Meaning-Making under the Putin Regime 750
Planetary Tectonism Across the Solar System 500
Petrology and Plate Tectonics 500
Writing Systems 500
A Handbook of User Experience Research & Design in Libraries 400
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 计算机科学 化学工程 生物化学 物理 内科学 复合材料 催化作用 光电子学 物理化学 电极 细胞生物学 基因 遗传学
热门帖子
关注 科研通微信公众号,转发送积分 6876614
求助须知:如何正确求助?哪些是违规求助? 8577318
关于积分的说明 18226193
捐赠科研通 6256289
什么是DOI,文献DOI怎么找? 3053561
关于科研通互助平台的介绍 2061576
邀请新用户注册赠送积分活动 2031283