间充质干细胞
基因沉默
成骨细胞
GNAS复合轨迹
小干扰RNA
细胞生物学
转染
癌症研究
RNA干扰
骨质疏松症
生物
体外
细胞培养
内分泌学
核糖核酸
基因
遗传学
作者
Genc Basha,Andrew Gregory Cottle,Thavaneetharajah Pretheeban,Karen Y. T. Chan,Dominik Witzigmann,Robert N. Young,Fábio Rossi,Pieter R. Cullis
标识
DOI:10.1016/j.ymthe.2022.06.012
摘要
Approved drugs for the treatment of osteoporosis can prevent further bone loss but do not stimulate bone formation. Approaches that improve bone density in metabolic diseases are needed. Therapies that take advantage of the ability of mesenchymal stem cells (MSCs) to differentiate into various osteogenic lineages to treat bone disorders are of particular interest. Here we examine the ability of small interfering RNA (siRNA) to enhance osteoblast differentiation and bone formation by silencing the negative suppressor gene GNAS in bone MSCs. Using clinically validated lipid nanoparticle (LNP) siRNA delivery systems, we show that silencing the suppressor gene GNAS in vitro in MSCs leads to molecular and phenotypic changes similar to those seen in osteoblasts. Further, we demonstrate that these LNP-siRNAs can transfect a large proportion of mice MSCs in the compact bone following intravenous injection. Transfection of MSCs in various animal models led to silencing of GNAS and enhanced differentiation of MSCs into osteoblasts. These data demonstrate the potential for LNP delivery of siRNA to enhance the differentiation of MSCs into osteoblasts, and suggests that they are a promising approach for the treatment of osteoporosis and other bone diseases.
科研通智能强力驱动
Strongly Powered by AbleSci AI