Comparison between USPIOs and SPIOs for Multimodal Imaging of Extracellular Vesicles Extracted from Adipose Tissue-Derived Adult Stem Cells

被引:0
作者
Capuzzo, Arnaud M. [1 ]
Piccolantonio, Giusi [2 ]
Negri, Alessandro [1 ]
Bontempi, Pietro [2 ]
Lacavalla, Maria A. [2 ,3 ]
Malatesta, Manuela [4 ]
Scambi, Ilaria [4 ]
Mariotti, Raffaella [4 ]
Luedtke-Buzug, Kerstin [5 ,6 ]
Corsi, Mauro [7 ]
Marzola, Pasquina [2 ]
机构
[1] Univ Verona, Dept Diagnost & Publ Hlth, Str Grazie 8, I-37134 Verona, Italy
[2] Univ Verona, Dept Engn Innovat Med, Str Grazie 15, I-37134 Verona, Italy
[3] Univ Padua, Dept Chem Sci, Via Marzolo 1, I-35131 Padua, Italy
[4] Univ Verona, Dept Neurosci Biomed & Movement Sci, Piazzale LA Scuro 10, I-37134 Verona, Italy
[5] Univ Lubeck, Inst Med Engn, Ratzeburger Allee 160, D-23562 Lubeck, Germany
[6] Fraunhofer Res Inst Individualized & Cell Based Me, D-23562 Lubeck, Germany
[7] Evotec Consultant, Via A Fleming 4, I-37135 Verona, Italy
关键词
MRI; regenerative medicine; iron nanoparticles; nanomedicine; extracellular vesicles; IN-VIVO TRACKING; IRON-OXIDE NANOPARTICLES; CONTRAST AGENTS; STROMAL CELLS; EFFICIENCY;
D O I
10.3390/ijms25179701
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Adipose tissue-derived adult stem (ADAS) cells and extracellular vesicle (EV) therapy offer promising avenues for treating neurodegenerative diseases due to their accessibility and potential for autologous cell transplantation. However, the clinical application of ADAS cells or EVs is limited by the challenge of precisely identifying them in specific regions of interest. This study compares two superparamagnetic iron oxide nanoparticles, differing mainly in size, to determine their efficacy for allowing non-invasive ADAS tracking via MRI/MPI and indirect labeling of EVs. We compared a USPIO (about 5 nm) with an SPIO (Resovist (R), about 70 nm). A physicochemical characterization of nanoparticles was conducted using DLS, TEM, MRI, and MPI. ADAS cells were labeled with the two nanoparticles, and their viability was assessed via MTT assay. MRI detected labeled cells, while TEM and Prussian Blue staining were employed to confirm cell uptake. The results revealed that Resovist (R) exhibited higher transversal relaxivity value than USPIO and, consequently, allows for detection with higher sensitivity by MRI. A 200 mu gFe/mL concentration was identified as optimal for ADAS labeling. MPI detected only Resovist (R). The findings suggest that Resovist (R) may offer enhanced detection of ADAS cells and EVs, making it suitable for multimodal imaging. Preliminary results obtained by extracting EVs from ADAS cells labeled with Resovist (R) indicate that EVs retain the nanoparticles, paving the way to an efficient and multimodal detection of EVs.
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页数:18
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