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pH 触发的金纳米颗粒聚集用于增强肺纤维化治疗中干细胞的标记和长期 CT 成像追踪。

pH-Triggered Aggregation of Gold Nanoparticles for Enhanced Labeling and Long-Term CT Imaging Tracking of Stem Cells in Pulmonary Fibrosis Treatment.

机构信息

CAS Key Laboratory of Nano-Bio Interface, Division of Nanobiomedicine, Suzhou Institute of Nano-Tech and Nano-bionics, Chinese Academy of Sciences, Suzhou, 215123, China.

School of Nano-Tech and Nano-Bionics, University of Science and Technology of China, Hefei, 230026, China.

出版信息

Small. 2021 Aug;17(33):e2101861. doi: 10.1002/smll.202101861. Epub 2021 Jul 8.

Abstract

Gold nanoparticles (AuNPs) pose a great challenge in the development of nanotracers that can self-adaptively alter their properties in response to certain cellular environments for long-term stem cell tracking. Herein, pH-sensitive Au nanotracers (CPP-PSD@Au) are fabricated by sequential coupling of AuNPs with sulfonamide-based polymer (PSD) and cell-penetrating peptide (CPP), which can be efficiently internalized by mesenchymal stem cells (MSCs) and undergo pH-induced self-assembly in endosomes, facilitating long-term computed tomography (CT) imaging tracking MSCs in a murine model of idiopathic pulmonary fibrosis (IPF). Using the CPP-PSD@Au, the transplanted MSCs for the first time can be monitored with CT imaging for up to 35 days after transplantation into the lung of IPF mice, clearly elucidating the migration process of MSCs in vivo. Moreover, we preliminarily explored the mechanism of the CPP-PSD@Au labeled MSCs in the alleviation of IPF, including recovery of alveolar integrity, decrease of collagen deposition, as well as down-regulation of relevant cytokine level. This work facilitates our understanding of the behavior and effect of MSCs in the therapy of IPF, thereby providing an important insight into the stem cell-based treatment of lung diseases.

摘要

金纳米颗粒 (AuNPs) 对纳米示踪剂的发展构成了巨大挑战,这些示踪剂能够自适应地改变其性质,以响应特定的细胞环境,从而实现长期的干细胞跟踪。在此,通过依次将金纳米颗粒与基于磺酰胺的聚合物 (PSD) 和细胞穿透肽 (CPP) 偶联,制备了 pH 敏感的 Au 纳米示踪剂 (CPP-PSD@Au),它可以被间充质干细胞 (MSCs) 高效内化,并在内涵体中发生 pH 诱导的自组装,有利于在特发性肺纤维化 (IPF) 小鼠模型中进行长期计算机断层扫描 (CT) 成像跟踪 MSC。使用 CPP-PSD@Au,首次可以通过 CT 成像监测移植到 IPF 小鼠肺部后的 MSC 长达 35 天,清楚地阐明了 MSC 在体内的迁移过程。此外,我们初步探讨了 CPP-PSD@Au 标记的 MSC 减轻 IPF 的机制,包括恢复肺泡完整性、减少胶原沉积以及下调相关细胞因子水平。这项工作有助于我们了解 MSC 在 IPF 治疗中的行为和作用,从而为基于干细胞的肺部疾病治疗提供了重要的见解。

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