小发夹RNA
慢病毒
基因沉默
离体
成骨细胞
RNA干扰
体内
细胞生物学
基因传递
功能(生物学)
基因
生物
化学
体外
遗传增强
基因敲除
免疫学
遗传学
核糖核酸
人类免疫缺陷病毒(HIV)
病毒性疾病
作者
Marc N. Wein,Dallas C. Jones,Laurie H. Glimcher
标识
DOI:10.1007/978-1-59745-104-8_11
摘要
Osteoblasts are the sole cell responsible for bone formation in vivo (1). Although genetic techniques have been extremely valuable to study the functions of certain genes in these cells in vivo, this approach is time consuming and expensive. An alternative loss-of-function approach that has been validated in many mammalian systems is shRNA-mediated gene silencing. This chapter describes methodology designed to introduce shRNA constructs into primary murine osteoblasts ex vivo in order to quickly assess the function of genes in osteoblast differentiation and extra cellular matrix mineralization. Both the production of shRNA-expressing lentiviruses and the infection of calvarial osteoblasts with these lentiviruses are detailed.
科研通智能强力驱动
Strongly Powered by AbleSci AI