CTGF公司
信使核糖核酸
寡核苷酸
结缔组织
纤维化
生长因子
转化生长因子
细胞生物学
疤痕
转染
成纤维细胞
信号转导
生物
分子生物学
癌症研究
受体
病理
基因
医学
体外
遗传学
作者
Mengjia Zheng,Christian Wiraja,David Yeo,Hao Chang,Daniel Chin Shiuan Lio,Wei Shi,Kanyi Pu,Amy S. Paller,Chenjie Xu
出处
期刊:Small
[Wiley]
日期:2018-10-24
卷期号:14 (49)
被引量:12
标识
DOI:10.1002/smll.201802546
摘要
Early diagnosis and timely intervention are key for the successful treatment of skin diseases like abnormal scars. This study introduces a nucleic-acid-based probe (i.e., molecular sprinkler) for the diagnosis and spontaneous regulation of the abnormal expression of fibrosis-related mRNA in scar-derived skin fibroblasts. Using mRNA encoding connective tissue growth factor (CTGF) as the model gene, a probe with three oligonucleotides is constructed, including a recognition sequence complementary to the CTGF mRNA, a siRNA against transforming growth factor receptor I (TGFβRI) as the CTGF mRNA suppressor, and a connecting sequence. The probe can detect CTGF mRNA with a limit of 10 × 10-9 m and distinguishes scar fibroblasts from normal ones in both 2D and 3D environments. Two days after transfection, the siRNA released from the probe reduces the expression of TGFβRI and, consequently, decreases the cellular expression of CTGF mRNA (up to 70%). This dual-role probe presents opportunities to monitor the TGF- β signaling pathway, screen for drugs that target the CTGF pathway, and determine the role of inhibition of the CTGF pathway in therapeutic efficacy.
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