Regulation of vascular smooth muscle cell autophagy by DNA nanotube-conjugated mTOR siRNA.

Abstract:

:The efficient delivery of short interfering RNA (siRNA) is an enormous challenge in the field of gene therapy. Herein, we report a delivery nanosystem based on programmed DNA self-assembly mammalian target of rapamycin (mTOR) siRNA-loaded DNA nanotubes (DNA-NTs). We demonstrate that these siRNA-DNA-NTs can be effectively transfected into pulmonary arterial smooth muscle cells (PASMCs) via endocytosis; and that the loaded mTOR siRNA can induce obvious autophagy and inhibit cell growth under both normal and hypoxic conditions. Moreover, we found that mTOR siRNA can control the autophagy and proliferation of PASMCs under hypoxic condition, suggesting a potential therapeutic application for mTOR siRNA in diseases involving abnormal autophagy in PASMCs.

journal_name

Biomaterials

journal_title

Biomaterials

authors

You Z,Qian H,Wang C,He B,Yan J,Mao C,Wang G

doi

10.1016/j.biomaterials.2015.07.015

subject

Has Abstract

pub_date

2015-10-01 00:00:00

pages

137-50

eissn

0142-9612

issn

1878-5905

pii

S0142-9612(15)00591-8

journal_volume

67

pub_type

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