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肽功能化纳米乳剂作为循环肿瘤细胞分离和体外培养的一种有前景的工具。

Peptide-Functionalized Nanoemulsions as a Promising Tool for Isolation and Ex Vivo Culture of Circulating Tumor Cells.

作者信息

Carmona-Ule Nuria, Gal Noga, Abuín Redondo Carmen, De La Fuente Freire María, López López Rafael, Dávila-Ibáñez Ana Belén

机构信息

Roche-Chus Joint Unit, Translational Medical Oncology Group (Oncomet), Health Research Institute of Santiago de Compostela (IDIS), Hospital Gil Casares, 15706 Santiago de Compostela, Spain.

Interdisciplinary Nanoscience Center (iNANO), Aarhus University, 8000 Aarhus, Denmark.

出版信息

Bioengineering (Basel). 2022 Aug 10;9(8):380. doi: 10.3390/bioengineering9080380.

Abstract

Circulating Tumor Cells (CTCs) are shed from primary tumors and travel through the blood, generating metastases. CTCs represents a useful tool to understand the biology of metastasis in cancer disease. However, there is a lack of standardized protocols to isolate and culture them. In our previous work, we presented oil-in-water nanoemulsions (NEs) composed of lipids and fatty acids, which showed a benefit in supporting CTC cultures from metastatic breast cancer patients. Here, we present Peptide-Functionalized Nanoemulsions (Pept-NEs), with the aim of using them as a tool for CTC isolation and culture in situ. Therefore, NEs from our previous work were surface-decorated with the peptides Pep10 and GE11, which act as ligands towards the specific cell membrane proteins EpCAM and EGFR, respectively. We selected the best surface to deposit a layer of these Pept-NEs through a Quartz Crystal Microbalance with Dissipation Monitoring (QCM-D) method. Next, we validated the specific recognition of Pept-NEs for their protein targets EpCAM and EGFR by QCM-D and fluorescence microscopy. Finally, a layer of Pept-NEs was deposited in a culture well-plate, and cells were cultured on for 9 days in order to confirm the feasibility of the Pept-NEs as a cell growth support. This work presents peptide-functionalized nanoemulsions as a basis for the development of devices for the isolation and culture of CTCs in situ due to their ability to specifically interact with membrane proteins expressed in CTCs, and because cells are capable of growing on top of them.

摘要

循环肿瘤细胞(CTCs)从原发性肿瘤脱落,通过血液转移,从而形成转移灶。CTCs是了解癌症转移生物学的有用工具。然而,目前缺乏分离和培养CTCs的标准化方案。在我们之前的工作中,我们展示了由脂质和脂肪酸组成的水包油纳米乳液(NEs),其对支持转移性乳腺癌患者的CTCs培养有益。在此,我们展示肽功能化纳米乳液(Pept-NEs),旨在将其用作原位分离和培养CTCs的工具。因此,我们用肽Pep10和GE11对之前工作中的NEs进行表面修饰,它们分别作为针对特定细胞膜蛋白EpCAM和EGFR的配体。我们通过具有耗散监测功能的石英晶体微天平(QCM-D)方法选择了最佳表面来沉积一层这些Pept-NEs。接下来,我们通过QCM-D和荧光显微镜验证了Pept-NEs对其蛋白质靶点EpCAM和EGFR的特异性识别。最后,在培养孔板中沉积一层Pept-NEs,并在其上培养细胞9天,以确认Pept-NEs作为细胞生长支持物的可行性。这项工作展示了肽功能化纳米乳液,由于其能够与CTCs中表达的膜蛋白特异性相互作用,且细胞能够在其表面生长,因此可作为原位分离和培养CTCs的装置开发基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2242/9405120/abeb4393ff84/bioengineering-09-00380-g001.jpg

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