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含有基因工程细菌的可注射微凝胶,用于通过程序性趋化因子表达进行结肠癌治疗。

Injectable microgels containing genetically engineered bacteria for colon cancer therapy through programmed Chemokine expression.

作者信息

Chen Yazhou, Cai Kehan, Zhao Hui, Li Wenshuai, Gao Xiaofang, Fu Yinzheng, Lee Kyubae, Li SiTian, Yao Shengjie, Chen Tao

机构信息

The First Affiliated Hospital of Zhengzhou University, Zhengzhou University, Zhengzhou, Henan, 450052, PR China.

Henan Institute of Advanced Technology, Zhengzhou University, Zhengzhou, Henan, 450003, PR China.

出版信息

Mater Today Bio. 2024 Nov 13;29:101337. doi: 10.1016/j.mtbio.2024.101337. eCollection 2024 Dec.

Abstract

Chemokines are emerging as important targets for cancer immunotherapy due to their role in regulating immune cell migration and activation within the tumor microenvironment. Effective delivery and sustained presence of chemokines at the tumor site is essential for recruiting and activating immune cells to exert anti-tumor effects. In this study, we report a genetically engineered bacterial cell factory designed for the continuous production of chemokine CCL21 in a controlled manner. To decrease the formation of infusion bodies (IBs) in bacteria, we used thioredoxin (Trx) as the fusion partner and cloned at N-terminal of the target protein. The commonly used promoters, pT7-LacO, pBV220, and pDawn, were employed to explore the influence of various inducers on the expression of CCL21 in bacteria. The engineered bacteria were finally encapsulated within spherical gelatin methacryloyl (GelMA) microgels, which not only maintained bacterial viability but also prolonged their retention in the intestines of mice. As a result, the sustained presence and localized production of CCL21 led to effective suppression of tumor growth.

摘要

趋化因子正成为癌症免疫治疗的重要靶点,因为它们在调节肿瘤微环境中免疫细胞的迁移和激活方面发挥着作用。趋化因子在肿瘤部位的有效递送和持续存在对于招募和激活免疫细胞以发挥抗肿瘤作用至关重要。在本研究中,我们报告了一种基因工程细菌细胞工厂,其设计用于以可控方式持续生产趋化因子CCL21。为了减少细菌中包涵体(IBs)的形成,我们使用硫氧还蛋白(Trx)作为融合伙伴,并将其克隆到靶蛋白的N端。使用常用的启动子pT7-LacO、pBV220和pDawn来探索各种诱导剂对细菌中CCL21表达的影响。最终,将工程菌封装在球形甲基丙烯酰化明胶(GelMA)微凝胶中,这不仅维持了细菌的活力,还延长了它们在小鼠肠道中的停留时间。结果,CCL21的持续存在和局部产生导致了对肿瘤生长的有效抑制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/825e/11609523/f1ddb9fde16d/ga1.jpg

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