Department of Clinical Laboratory Medicine, Southwest Hospital, Third Military Medical University (Army Medical University), 30 Gaotanyan, Shapingba, Chongqing 400038, China.
Department of General Surgery, Xinqiao Hospital, Army Medical University, Chongqing 400037, China.
ACS Nano. 2024 May 28;18(21):13950-13965. doi: 10.1021/acsnano.4c04147. Epub 2024 May 15.
Manipulating the expression of cellular genes through efficient CRISPR/Cas9 delivery is rapidly evolving into a desirable tumor therapeutics. The exposure of CRISPR/Cas9 to a complex external environment poses challenges for conventional delivery carriers in achieving responsive and accurate release. Here, we report a Trojan horse-like nanocapsule for the on-demand delivery of CRISPR/Cas9 in a microRNA-responsive manner, enabling precise tumor therapy. The nanocapsule comprises a nanoassembled, engineered DNAzyme shell encasing a Cas9/sgRNA complex core. The DNAzyme, functioning as a catalytic unit, undergoes a conformational change in the presence of tumor-associated microRNA, followed by activating a positive feedback-driven autonomous catabolic cycle of the nanocapsule shell. This catabolic cycle is accomplished through chain reactions of DNAzyme "cleavage-hybridization-cleavage", which ensures sensitivity in microRNA recognition and effective release of Cas9/sgRNA. Utilizing this Trojan horse-like nanocapsule, as low as 1.7 pM microRNA-21 can trigger the on-demand release of Cas9/sgRNA, enabling the specific editing of the protumorigenic microRNA coding gene. The resulting upregulation of tumor suppressor genes induces apoptosis in tumor cells, leading to significant inhibition of tumor growth by up to 75.94%. The Trojan horse-like nanocapsule, with superior programmability and biocompatibility, is anticipated to serve as a promising carrier for tailoring responsive gene editing systems, achieving enhanced antitumor specificity and efficacy.
通过高效的 CRISPR/Cas9 递送来操纵细胞基因的表达正在迅速发展成为一种理想的肿瘤治疗方法。CRISPR/Cas9 暴露于复杂的外部环境给传统的递送载体在实现响应性和准确释放方面带来了挑战。在这里,我们报告了一种类似于特洛伊木马的纳米胶囊,用于以 miRNA 响应的方式按需递送 CRISPR/Cas9,从而实现精确的肿瘤治疗。该纳米胶囊由纳米组装的工程 DNAzyme 壳封装 Cas9/sgRNA 复合物核心组成。DNAzyme 作为催化单元,在存在与肿瘤相关的 microRNA 时会发生构象变化,随后激活纳米胶囊壳的正反馈驱动的自主分解循环。这种分解循环是通过 DNAzyme“切割-杂交-切割”的链式反应来完成的,这确保了对 microRNA 识别的敏感性和 Cas9/sgRNA 的有效释放。利用这种类似于特洛伊木马的纳米胶囊,低至 1.7 pM 的 microRNA-21 即可触发 Cas9/sgRNA 的按需释放,从而能够特异性编辑致癌 microRNA 编码基因。由此引起的肿瘤抑制基因的上调诱导肿瘤细胞凋亡,导致肿瘤生长抑制高达 75.94%。这种类似于特洛伊木马的纳米胶囊具有优越的可编程性和生物相容性,有望成为定制响应性基因编辑系统的有前途的载体,从而提高抗肿瘤的特异性和疗效。