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基于四面体框架核酸的微小RNA-155递送通过调节巨噬细胞极化抑制脉络膜新生血管形成。

Tetrahedral framework nucleic acids-based delivery of microRNA-155 inhibits choroidal neovascularization by regulating the polarization of macrophages.

作者信息

Qin Xin, Xiao Lirong, Li Ni, Hou Chen, Li Wenman, Li Jiajie, Yan Naihong, Lin Yunfeng

机构信息

State Key Laboratory of Oral Diseases, National Clinical Research Center for Oral Diseases, West China Hospital of Stomatology, Sichuan University, Chengdu, 610041, China.

Research Laboratory of Ophthalmology, West China Hospital, Sichuan University, Chengdu, 610041, China.

出版信息

Bioact Mater. 2021 Dec 18;14:134-144. doi: 10.1016/j.bioactmat.2021.11.031. eCollection 2022 Aug.

Abstract

Choroidal neovascularization (CNV) is a common pathological feature of various eye diseases and an important cause of visual impairment in middle-aged and elderly patients. In previous studies, tetrahedral framework nucleic acids (tFNAs) showed good carrier performance. In this experiment, we developed microRNA-155-equipped tFNAs (T-155) and explored its biological effects on CNV. Based on the results of in-vitro experiments, T-155 could regulate macrophages into the antiangiogenic M1 type. Then, we injected T-155 into the vitreous of laser-induced CNV model mice and found that T-155 significantly reduced the size and area of CNV, inhibited blood vessel leakage. In summary, we prove that T-155 could regulate the inflammatory process of CNV by polarizing macrophages, thereby improving the symptoms of CNV. Thus, T-155 might become a new DNA-based drug with great potential for treating CNV.

摘要

脉络膜新生血管(CNV)是多种眼部疾病的常见病理特征,也是中老年患者视力损害的重要原因。在以往的研究中,四面体框架核酸(tFNA)表现出良好的载体性能。在本实验中,我们开发了配备微小RNA-155的tFNA(T-155),并探讨了其对CNV的生物学作用。基于体外实验结果,T-155可将巨噬细胞调节为抗血管生成的M1型。然后,我们将T-155注射到激光诱导的CNV模型小鼠的玻璃体中,发现T-155显著减小了CNV的大小和面积,抑制了血管渗漏。综上所述,我们证明T-155可通过使巨噬细胞极化来调节CNV的炎症过程,从而改善CNV的症状。因此,T-155可能成为一种具有巨大治疗CNV潜力的新型DNA药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e1bb/8892086/25e278fb26a0/ga1.jpg

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