Fruit exosome-like particles for therapeutic delivery of extracellular miRNAs

用于治疗性递送细胞外 miRNA 的水果外泌体样颗粒

• 批准号: 9060653
• 负责人: PEIXUAN GUO
• 金额: $ 7.5万
• 依托单位: UNIVERSITY OF LOUISVILLE
• 依托单位国家: 美国
• 财政年份: 2013
• 资助国家: 美国
• 起止时间: 2013-08-01 至 2018-07-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/9060653
• 关键词: Adverse effects; Animals; Antibodies; Biohazardous Substance; Biological Assay; Brain; Brain Neoplasms; Breast; Cells; Clinic; Clinical; Colon Carcinoma; Colonic Neoplasms; Curcumin; DNA; Data; Dendritic Cells; Development; Disease; Dose; Down-Regulation; Edible Plants; Encapsulated; Environment; Evaluation; Folic Acid; Fruit; Gene Expression; Goals; Grapefruit; Grapes; Health; Human; Immune response; Immunotherapy; In Vitro; Inflammatory; Intranasal Administration; Knock-in Mouse; Knock-out; Laboratories; Light; Lipids; Liposomes; Literature; Liver; MHC Class I Genes; Malignant Neoplasms; Mammalian Cell; Metastatic Neoplasm to the Liver; MicroRNAs; Modeling; Mus; Myelogenous; Myeloid Cells; NK Cell Activation; Neoplasm Metastasis; Non-Viral Vector; Nucleic Acids; Oral Administration; Paclitaxel; Pharmaceutical Preparations; Phenotype; Play; Prevention; Production; Proteins; Protocols documentation; Publishing; RNA; Research Personnel; Role; Safety; Science; Signal Transduction; Small Interfering RNA; Small RNA; Specificity; Suppressor-Effector T-Lymphocytes; System; Testing; Therapeutic; Therapeutic Agents; Tissues; Tomatoes; Toxic effect; Tumor Tissue; Viral Vector; aqueous; base; cancer cell; cancer therapy; cell type; chemotherapeutic agent; chemotherapy; cost; expression vector; extracellular; in vivo; intravenous administration; killings; large scale production; migration; mouse model; nanoparticle; nanosized; nanovector; neoplastic cell; overexpression; particle; prevent; receptor; targeted delivery; therapeutic miRNA; tool; trafficking; tumor; vector-induced

DESCRIPTION (provided by applicant): The overall goal of this proposal is to develop exosome-like nanoparticles as a delivery vehicle for targetable delivery of extracellular RNA (exRNA) primarily focusing on miRNAs which modulate gene expression and induce immune responses upon delivery in mouse tumor models. Development of exRNA-based therapeutics must overcome challenges including issues of delivery, potential off-target effects, safety, toxicity, the cost of large scale production, elimination of potential biohazards to the environmen and tissue specificity. Unlike the situation with artificially synthesized nanoparticles or liposomes, naturally derived nanoparticle-size exosomes are released from many different types of cells. miRNAs and RNAs can be encapsulated in naturally derived exosomes and the RNAs are stable, and a number of miRNAs can be naturally encapsulated simultaneously in these exosomes. Recently, data published by ours and other groups have demonstrated that mammalian exosomes can deliver poorly soluble agents, chemotherapeutic drugs, and siRNA in vivo. A limitation of this mode is the need for large-scale production of exosomes, and potential biosafety. Our preliminary data show that exosome-like nanoparticles can be isolated in large quantities from the tissue of edible plants, including grapes. We have demonstrated that exosome-like nanoparticles from grapes are composed of small RNAs, proteins, and lipids. An edible plant-derived nano-vector (EPNV) assembled from grape exosome-like derived lipids is capable of encapsulating siRNAs. Co-delivery of folic acid, with the chemotherapy drug paclitaxel by EPNVs results in an increased efficiency in tumor tissue targeting. Reducing the size of EPNVs by passing them through an appropriate pore size filter significantly enhances EPNV translocation to the brain and oral administration of the EPNVs results in their migration to the liver. Based on these preliminary data and the current literature, we propose to: (1) Determine whether an EPNV can deliver therapeutic miR17 via oral administration to target metastatic colon tumor in the liver, subsequently inducing NK cell activation to kill metastatic tumor cells; (2) Determine whether miR155 encapsulated in EPNV promotes differentiation of myeloid derived suppressor cells (MDSCs) into mature dendritic cells in mouse breast/brain tumor models; (3) Determine whether a therapeutic dose of miRNA17 or miRNA155 delivered by EPNV induces no side-effects in mouse tumor models; and (4) Determine whether EPNV can be produced in large scale amounts economically for use in clinical settings. Demonstration of using a EPNV-based delivery system loaded with a desired therapeutic extracellular RNA (exRNA) including microRNA to target to inflammatory cells and tumor cells in vivo would not only be a significant step forward in the treatment of cancer, but also provide a powerful tool for identifying the role and effects of each small RNA encapsulated in resident or circulating microvesicles on the recipient cells. We will accomplish this in our study by knock-out and knock-in strategies.

描述（由申请人提供）：本提案的总体目标是开发外泌体样纳米颗粒作为可靶向递送细胞外RNA （exRNA）的递送载体，主要关注在小鼠肿瘤模型中递送时调节基因表达和诱导免疫反应的mirna。开发基于exrna的疗法必须克服各种挑战，包括递送、潜在的脱靶效应、安全性、毒性、大规模生产的成本、消除对环境的潜在生物危害和组织特异性等问题。与人工合成纳米颗粒或脂质体的情况不同，天然衍生的纳米颗粒大小的外泌体可以从许多不同类型的细胞中释放出来。mirna和rna可以被包裹在天然衍生的外泌体中，并且rna是稳定的，并且许多mirna可以同时被自然地包裹在这些外泌体中。最近，我们和其他小组发表的数据表明，哺乳动物外泌体可以在体内递送难溶性药物、化疗药物和siRNA。这种模式的一个限制是需要大规模生产外泌体，以及潜在的生物安全性。我们的初步数据表明，类外泌体纳米颗粒可以从包括葡萄在内的可食用植物的组织中大量分离出来。我们已经证明来自葡萄的外泌体样纳米颗粒由小rna、蛋白质和脂质组成。由葡萄外泌体样衍生脂质组装而成的可食用植物源性纳米载体（EPNV）能够封装sirna。叶酸与化疗药物紫杉醇由EPNVs共同递送，可提高肿瘤组织靶向的效率。通过适当的孔径过滤器来减小EPNV的大小，可显著增强EPNV向大脑的转运，口服EPNV可导致其向肝脏的迁移。基于这些初步数据和现有文献，我们建议：(1)确定EPNV是否可以通过口服给药靶向肝脏转移性结肠肿瘤，随后诱导NK细胞活化，杀死转移性肿瘤细胞；(2)在小鼠乳腺/脑肿瘤模型中，确定EPNV包封的miR155是否促进髓源性抑制细胞（MDSCs）向成熟树突状细胞的分化；(3)确定EPNV给药治疗剂量的miRNA17或miRNA155在小鼠肿瘤模型中是否无副作用；(4)确定是否可以经济地大规模生产新冠病毒以供临床使用。使用基于epv的递送系统装载所需的治疗性细胞外RNA (exRNA)，包括microRNA，在体内靶向炎症细胞和肿瘤细胞，不仅是癌症治疗的重要一步，而且还提供了一个强大的工具