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蛋白质冠层在氟化纳米颗粒的细胞摄取中起关键作用,对F-MR成像具有更高的灵敏度。

Pivotal role of the protein corona in the cell uptake of fluorinated nanoparticles with increased sensitivity for F-MR imaging.

作者信息

Gatti Lodovico, Chirizzi Cristina, Rotta Giulia, Milesi Pietro, Sancho-Albero María, Sebastián Victor, Mondino Anna, Santamaría Jesús, Metrangolo Pierangelo, Chaabane Linda, Bombelli Francesca Baldelli

机构信息

Department of Chemistry, Materials and Chemical Engineering "Giulio Natta" Politecnico di Milano, 32 Milano 20131 Italy

Institute of Experimental Neurology (INSpe) and Experimental Imaging Center (CIS), IRCCS San Raffaele Scientific Institute Via Olgettina, 58 Milano 20132 Italy

出版信息

Nanoscale Adv. 2023 Jun 8;5(14):3749-3760. doi: 10.1039/d3na00229b. eCollection 2023 Jul 11.


DOI:10.1039/d3na00229b
PMID:37441254
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10334373/
Abstract

cell tracking by non-invasive imaging technologies is needed to accelerate the clinical translation of innovative cell-based therapies. In this regard, F-MRI has recently gained increased attention for unbiased localization of labeled cells over time. To push forward the use of F-MRI for cell tracking, the development of highly performant F-probes is required. PLGA-based NPs containing PERFECTA, a multibranched superfluorinated molecule with an optimal MRI profile thanks to its 36 magnetically equivalent fluorine atoms, are promising F-MRI probes. In this work we demonstrate the importance of the surface functionalization of these NPs in relation to their interaction with the biological environment, stressing the pivotal role of the formation of the protein corona (PC) in their cellular labelling efficacy. In particular, our studies showed that the formation of PC NPs strongly promotes the cellular internalization of these NPs in microglia cells. We advocate that the formation of PC NPs in the culture medium can be a key element to be used for the optimization of cell labelling with a considerable increase of the detection sensitivity by F-MRI.

摘要

为加速基于细胞的创新疗法的临床转化,需要通过非侵入性成像技术进行细胞追踪。在这方面,F - MRI最近因能随时间对标记细胞进行无偏定位而受到越来越多的关注。为推动F - MRI在细胞追踪中的应用,需要开发高性能的F - 探针。含有PERFECTA的基于聚乳酸 - 羟基乙酸共聚物(PLGA)的纳米颗粒(NPs)是很有前景的F - MRI探针,PERFECTA是一种多分支超氟化分子,因其36个磁等效氟原子而具有最佳的磁共振成像(MRI)谱。在这项工作中,我们证明了这些纳米颗粒的表面功能化与其与生物环境相互作用的相关性的重要性,强调了蛋白质冠(PC)的形成在其细胞标记功效中的关键作用。特别是,我们的研究表明,PC纳米颗粒的形成强烈促进了这些纳米颗粒在小胶质细胞中的细胞内化。我们主张,在培养基中形成PC纳米颗粒可能是用于优化细胞标记的关键因素,通过F - MRI可显著提高检测灵敏度。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/22c2/10334373/587dc6820e78/d3na00229b-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/22c2/10334373/a305cccf0f76/d3na00229b-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/22c2/10334373/3613344b1a89/d3na00229b-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/22c2/10334373/9f659ccf631c/d3na00229b-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/22c2/10334373/c1556a223dd4/d3na00229b-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/22c2/10334373/587dc6820e78/d3na00229b-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/22c2/10334373/a305cccf0f76/d3na00229b-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/22c2/10334373/3613344b1a89/d3na00229b-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/22c2/10334373/9f659ccf631c/d3na00229b-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/22c2/10334373/c1556a223dd4/d3na00229b-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/22c2/10334373/587dc6820e78/d3na00229b-f5.jpg

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[1]
Pivotal role of the protein corona in the cell uptake of fluorinated nanoparticles with increased sensitivity for F-MR imaging.

Nanoscale Adv. 2023-6-8

[2]
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[3]
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[5]
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[6]
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[7]
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引用本文的文献

[1]
Study of Hard Protein Corona on Lipid Surface of Composite Nanoconstruction.

Nanomaterials (Basel). 2024-11-4

本文引用的文献

[1]
The protein corona from nanomedicine to environmental science.

Nat Rev Mater. 2023-3-24

[2]
Water-Soluble Chemically Precise Fluorinated Molecular Clusters for Interference-Free Multiplex F MRI in Living Mice.

ACS Nano. 2023-3-14

[3]
Optimization of superfluorinated PLGA nanoparticles for enhanced cell labelling and detection by F-MRI.

Colloids Surf B Biointerfaces. 2022-12

[4]
Multispectral fluorine-19 MRI enables longitudinal and noninvasive monitoring of tumor-associated macrophages.

Sci Transl Med. 2022-10-19

[5]
Effect of molecular crowding on the biological identity of liposomes: an overlooked factor at the bio-nano interface.

Nanoscale Adv. 2019-5-31

[6]
Fluorine MR Imaging Probes Dynamic Migratory Profiles of Perfluorocarbon-Loaded Dendritic Cells After Streptozotocin-Induced Inflammation.

Mol Imaging Biol. 2022-4

[7]
Correlating Corona Composition and Cell Uptake to Identify Proteins Affecting Nanoparticle Entry into Endothelial Cells.

ACS Biomater Sci Eng. 2021-12-13

[8]
Biological Utility of Fluorinated Compounds: from Materials Design to Molecular Imaging, Therapeutics and Environmental Remediation.

Chem Rev. 2022-1-12

[9]
A Bioorthogonal Probe for Multiscale Imaging by F-MRI and Raman Microscopy: From Whole Body to Single Cells.

J Am Chem Soc. 2021-8-11

[10]
Delivery Systems for Nucleic Acids and Proteins: Barriers, Cell Capture Pathways and Nanocarriers.

Pharmaceutics. 2021-3-22

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