Effective and Safe Gene Delivery to the Mouse Kidney <em>via</em> Slow Retrograde Renal Pelvis Injection of Adeno-Associated Virus Vectors

基因传递 肾盂 腺相关病毒 基因 病毒 医学 遗传增强 病毒学 生物 内科学 载体(分子生物学) 遗传学 重组DNA
作者
Hideyuki Hakui,Anusha Sairavi,Ranjan Das,Taisuke Furusho,Hiroyuki Nakai
出处
期刊:Journal of Visualized Experiments [MyJOVE]
卷期号: (222)
标识
DOI:10.3791/67716
摘要

The development of effective in vivo tools and methods for gene delivery to the kidney is crucial for advancing basic kidney research and gene therapy for kidney diseases. In addition, growing awareness of monogenic kidney diseases, driven by advanced genetic testing, underscores the potential of gene therapy to treat and even cure difficult-to-treat genetic kidney diseases. In this regard, adeno-associated virus (AAV) vectors have garnered increasing attention as a robust platform for in vivo gene delivery; however, the most effective and safest method for AAV vector-mediated gene delivery to each therapeutically relevant cell type in the kidney has not yet been fully established. Here, the method of slow retrograde renal pelvis (RP) injection of AAV vectors is detailed, and its high potential to transduce mouse kidneys is demonstrated when used with appropriately selected AAV capsids. Moreover, this method is shown to be effective not only with the standard cesium chloride ultracentrifugation-purified AAV (CsCl AAV) vectors but also with centrifugally ultrafiltered AAV (CU AAV) vector minipreps, which can be prepared rapidly and simply using techniques that do not require specialized AAV vector expertise. As an example, this study demonstrates slow RP injection of both CsCl and CU AAV-KP3 vectors results in robust transduction of proximal tubules in the mouse kidney with no apparent tissue damage, unlike previously reported hydrodynamic approaches that inevitably lead to tissue damage. Thus, this study highlights that slow retrograde RP injection of select AAV capsid-derived vectors is an effective and safe method for gene delivery to the kidney. This method will be applicable to a broad spectrum of kidney research, including gene therapy studies. The use of CU AAV vector minipreps will significantly increase throughput and improve the time and cost efficiency needed to generate preliminary data and obtain crucial insights.
最长约 10秒,即可获得该文献文件

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
yy完成签到,获得积分10
1秒前
RIkka完成签到,获得积分10
2秒前
LINJMX完成签到 ,获得积分10
2秒前
xyx2999完成签到,获得积分10
3秒前
sherry完成签到,获得积分10
3秒前
光亮的书文完成签到,获得积分10
3秒前
coconut完成签到,获得积分10
3秒前
小鹅0729完成签到,获得积分10
3秒前
小马想毕业完成签到,获得积分10
3秒前
leinuo077完成签到,获得积分10
4秒前
筱星完成签到,获得积分10
4秒前
小宝完成签到,获得积分10
5秒前
好运来完成签到,获得积分10
7秒前
Qingzhu完成签到,获得积分10
7秒前
AW完成签到,获得积分10
8秒前
窦誉应助徐子扬采纳,获得10
8秒前
俗丨完成签到,获得积分10
8秒前
小小完成签到 ,获得积分10
8秒前
洪小乖完成签到,获得积分10
8秒前
权秋尽完成签到,获得积分10
8秒前
kaka091完成签到,获得积分10
9秒前
秋归晚完成签到,获得积分10
9秒前
ZGY完成签到,获得积分10
9秒前
Jenny完成签到,获得积分10
9秒前
Oil完成签到,获得积分10
9秒前
周雪峰完成签到,获得积分10
10秒前
Qqiao完成签到 ,获得积分10
11秒前
忧伤的绍辉完成签到 ,获得积分10
11秒前
雨寒完成签到 ,获得积分10
11秒前
12秒前
Dewcy完成签到,获得积分20
12秒前
15秒前
思源应助MSY采纳,获得10
16秒前
科研乞丐完成签到,获得积分10
16秒前
维维逗奶完成签到,获得积分10
16秒前
liuchuck完成签到 ,获得积分10
16秒前
eagle14835完成签到,获得积分10
17秒前
碧蓝可乐完成签到,获得积分10
17秒前
一切顺利完成签到 ,获得积分10
17秒前
毛毛余完成签到 ,获得积分10
18秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
晶种分解过程与铝酸钠溶液混合强度关系的探讨 8888
Chemistry and Physics of Carbon Volume 18 800
The Organometallic Chemistry of the Transition Metals 800
Leading Academic-Practice Partnerships in Nursing and Healthcare: A Paradigm for Change 800
The formation of Australian attitudes towards China, 1918-1941 640
Signals, Systems, and Signal Processing 610
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 化学工程 生物化学 计算机科学 物理 内科学 复合材料 催化作用 物理化学 光电子学 电极 细胞生物学 基因 无机化学
热门帖子
关注 科研通微信公众号,转发送积分 6428221
求助须知:如何正确求助?哪些是违规求助? 8244874
关于积分的说明 17529122
捐赠科研通 5483812
什么是DOI,文献DOI怎么找? 2895256
邀请新用户注册赠送积分活动 1871443
关于科研通互助平台的介绍 1710701