Rhodamine bound maghemite as a long-term dual imaging nanoprobe of adipose tissue-derived mesenchymal stromal cells
Language English Country Germany Media print-electronic
Document type Journal Article
PubMed
27889810
DOI
10.1007/s00249-016-1187-1
PII: 10.1007/s00249-016-1187-1
Knihovny.cz E-resources
- Keywords
- Confocal microscopy, Dual contrast agents, Intracellular fluorescent labels, Iron oxide nanoparticles, Mesenchymal stromal cells, Rhodamine, Stem cell tracking,
- MeSH
- Dextrans metabolism MeSH
- Spectrometry, Fluorescence MeSH
- Intracellular Space metabolism MeSH
- Humans MeSH
- Magnetite Nanoparticles chemistry MeSH
- Mesenchymal Stem Cells cytology metabolism MeSH
- Molecular Probes chemistry metabolism MeSH
- Molecular Imaging methods MeSH
- Rhodamines chemistry MeSH
- Adipose Tissue cytology MeSH
- Cell Survival MeSH
- Check Tag
- Humans MeSH
- Male MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- Dextrans MeSH
- ferumoxides MeSH Browser
- Magnetite Nanoparticles MeSH
- Molecular Probes MeSH
- Rhodamines MeSH
In the last few years, magnetically labeled cells have been intensively explored, and non-invasive cell tracking and magnetic manipulation methods have been tested in preclinical studies focused on cell transplantation. For clinical applications, it is desirable to know the intracellular pathway of nanoparticles, which can predict their biocompatibility with cells and the long-term imaging properties of labeled cells. Here, we quantified labeling efficiency, localization, and fluorescence properties of Rhodamine derivatized superparamagnetic maghemite nanoparticles (SAMN-R) in mesenchymal stromal cells (MSC). We investigated the stability of SAMN-R in the intracellular space during a long culture (20 days). Analyses were based on advanced confocal microscopy accompanied by atomic absorption spectroscopy (AAS) and magnetic resonance imaging. SAMN-R displayed excellent cellular uptake (24 h of labeling), and no toxicity of SAMN-R labeling was found. 83% of SAMN-R nanoparticles were localized in lysosomes, only 4.8% were found in mitochondria, and no particles were localized in the nucleus. On the basis of the MSC fluorescence measurement every 6 days, we also quantified the continual decrease of SAMN-R fluorescence in the average single MSC during 18 days. An additional set of analyses showed that the intracellular SAMN-R signal decrease was minimally caused by fluorophore degradation or nanoparticles extraction from the cells, main reason is a cell division. The fluorescence of SAMN-R nanoparticles within the cells was detectable minimally for 20 days. These observations indicate that SAMN-R nanoparticles have a potential for application in transplantation medicine.
Department of Biomedical Engineering FEEC Brno University of Technology Brno Czech Republic
Department of Comparative Biomedicine and Food Science University of Padua Padua Italy
Institute of Scientific Instruments The Czech Academy of Sciences Brno Czech Republic
International Clinical Research Center St Anne's University Hospital Brno Brno Czech Republic
See more in PubMed
Pharm Res. 1997 Nov;14(11):1568-73 PubMed
Cytotherapy. 2013 Mar;15(3):307-22 PubMed
Phys Chem Chem Phys. 2013 Feb 21;15(7):2282-90 PubMed
Mol Imaging Biol. 2011 Jun;13(3):443-451 PubMed
Spectrochim Acta A Mol Biomol Spectrosc. 2014;121:147-51 PubMed
NMR Biomed. 2004 Nov;17 (7):513-7 PubMed
Angew Chem Int Ed Engl. 2011 Feb 7;50(6):1242-58 PubMed
Biomaterials. 2012 Feb;33(5):1477-88 PubMed
J Orthop Res. 2012 Sep;30(9):1499-506 PubMed
Pharmacol Res. 2010 Aug;62(2):126-43 PubMed
Int J Nanomedicine. 2015 Mar 02;10:1679-90 PubMed
Nat Biotechnol. 2000 Apr;18(4):410-4 PubMed
J Biosci Bioeng. 2002;94(6):606-13 PubMed
Biomaterials. 2013 Feb;34(7):1772-80 PubMed
Int J Pharm. 2011 Jan 17;403(1-2):139-61 PubMed
Small. 2010 Jan;6(1):12-21 PubMed
Br J Radiol. 2015 Oct;88(1054):20150375 PubMed
Micron. 2014 Dec;67:149-154 PubMed
Radiology. 2003 Sep;228(3):760-7 PubMed
Cytotherapy. 2009;11(1):43-51 PubMed
Acta Biomater. 2012 Jul;8(6):2068-76 PubMed
Adv Healthc Mater. 2014 Feb;3(2):176-81 PubMed
Int J Nanomedicine. 2014 Nov 20;9:5355-72 PubMed
Biochem Biophys Res Commun. 2008 May 16;369(4):1076-81 PubMed
Magn Reson Med. 2003 Jun;49(6):1006-13 PubMed
Int J Nanomedicine. 2012;7:2249-59 PubMed