基因沉默
炎症
癌症研究
背景(考古学)
细胞周期蛋白D1
细胞生物学
小干扰RNA
免疫学
生物
细胞周期
癌症
转染
细胞培养
基因
遗传学
古生物学
作者
Dan Peer,Eun Jeong Park,Yoshiyuki Morishita,Christopher V. Carman,Motomu Shimaoka
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:2008-02-01
卷期号:319 (5863): 627-630
被引量:475
标识
DOI:10.1126/science.1149859
摘要
Cyclin D1 (CyD1) is a pivotal cell cycle–regulatory molecule and a well-studied therapeutic target for cancer. Although CyD1 is also strongly up-regulated at sites of inflammation, its exact roles in this context remain uncharacterized. To address this question, we developed a strategy for selectively silencing CyD1 in leukocytes in vivo. Targeted stabilized nanoparticles (tsNPs) were loaded with CyD1–small interfering RNA (siRNA). Antibodies to β 7 integrin (β 7 I) were then used to target specific leukocyte subsets involved in gut inflammation. Systemic application of β 7 I-tsNPs silenced CyD1 in leukocytes and reversed experimentally induced colitis in mice by suppressing leukocyte proliferation and T helper cell 1 cytokine expression. This study reveals CyD1 to be a potential anti-inflammatory target, and suggests that the application of similar modes of targeting by siRNA may be feasible in other therapeutic settings.
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