Star-shaped copolypeptide-mediated transfection of 3D organoids

IF 6.3 2区 化学 Q1 POLYMER SCIENCE European Polymer Journal Pub Date : 2025-04-15 DOI:10.1016/j.eurpolymj.2025.113932
Shiang-Ting Huang , Yu-Fon Chen , Yi-Cheng Chen , Jing-Ting Lin , Chao-Ling Yao , Jeng-Shiung Jan
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Abstract

While gene therapy offers hope for treating genetic disorders and cancer, efficient and targeted gene delivery continues to be a significant hurdle. This study introduces star-shaped block copolypeptides as novel gene carriers capable of directly transfecting entire cell clusters within three-dimensional (3D) organoid models. Star-shaped poly(L-lysine)-block-poly(L-alanine) (s-PLL-PLA) polypeptides with various arm numbers were synthesized and their potentiality as non-viral gene carriers was evaluated. Our experimental results revealed that the transfection efficiency of s-PLL-PLA/plasmid polyplexes rivaled that of the commercial standard, Lipofectamine 2000, also highlighting the importance of using 3D organoids to mimic the structure and function of native tissues. The s-PLL-PLA polypeptides exhibited amphiphilicity and steric hindrance imposed by the presence of rigid, hydrophobic PLA segment on the star architecture, rendering the improved biocompatibility and transfection efficiency due to the charge shielding and less dense packing with the plasmids. By targeting HSP90 AB1, an oncogene associated with aggressive cancer progression and poor patient outcomes, the s-PLL-PLA/short hairpin RNA (shRNA) polyplexes exhibited potent anticancer efficacy via the effective suppression of MDA-MB-231 breast cancer cell proliferation and then the induction of apoptosis. These findings strongly suggest that s-PLL-PLA polypeptides hold promise as effective non-viral gene delivery systems for inducing cancer cell apoptosis.

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星形共肽介导的三维类器官转染
虽然基因疗法为治疗遗传性疾病和癌症带来了希望,但有效和有针对性的基因传递仍然是一个重大障碍。该研究引入了星形嵌段共肽作为新型基因载体,能够直接转染三维(3D)类器官模型中的整个细胞簇。合成了不同臂数的星形聚(l -赖氨酸)-块聚(l -丙氨酸)(s-PLL-PLA)多肽,并评价了其作为非病毒基因载体的潜力。我们的实验结果显示,s-PLL-PLA/质粒多聚体的转染效率与商业标准Lipofectamine 2000相媲美,也强调了使用3D类器官模拟天然组织结构和功能的重要性。s-PLL-PLA多肽表现出两亲性和空间位阻,这是由于在星形结构上存在刚性的疏水性PLA片段,由于电荷屏蔽和与质粒的密度较小,从而提高了生物相容性和转染效率。通过靶向HSP90 AB1, s-PLL-PLA/短发夹RNA (shRNA)复合物通过有效抑制MDA-MB-231乳腺癌细胞增殖并诱导凋亡,显示出强大的抗癌功效。HSP90 AB1是一种与侵袭性癌症进展和不良患者预后相关的癌基因。这些发现强烈表明,s-PLL-PLA多肽有望成为诱导癌细胞凋亡的有效非病毒基因传递系统。
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来源期刊
European Polymer Journal
European Polymer Journal 化学-高分子科学
CiteScore
9.90
自引率
10.00%
发文量
691
审稿时长
23 days
期刊介绍: European Polymer Journal is dedicated to publishing work on fundamental and applied polymer chemistry and macromolecular materials. The journal covers all aspects of polymer synthesis, including polymerization mechanisms and chemical functional transformations, with a focus on novel polymers and the relationships between molecular structure and polymer properties. In addition, we welcome submissions on bio-based or renewable polymers, stimuli-responsive systems and polymer bio-hybrids. European Polymer Journal also publishes research on the biomedical application of polymers, including drug delivery and regenerative medicine. The main scope is covered but not limited to the following core research areas: Polymer synthesis and functionalization • Novel synthetic routes for polymerization, functional modification, controlled/living polymerization and precision polymers. Stimuli-responsive polymers • Including shape memory and self-healing polymers. Supramolecular polymers and self-assembly • Molecular recognition and higher order polymer structures. Renewable and sustainable polymers • Bio-based, biodegradable and anti-microbial polymers and polymeric bio-nanocomposites. Polymers at interfaces and surfaces • Chemistry and engineering of surfaces with biological relevance, including patterning, antifouling polymers and polymers for membrane applications. Biomedical applications and nanomedicine • Polymers for regenerative medicine, drug delivery molecular release and gene therapy The scope of European Polymer Journal no longer includes Polymer Physics.
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