Labeling Efficacy of Superparamagnetic Iron Oxide Nanoparticles to Human Neural Stem Cells: Comparison of Ferumoxides, Monocrystalline Iron Oxide, Cross-linked Iron Oxide (CLIO)-NH2 and tat-CLIO
Korean Journal of Radiology
; : 365-371, 2007.
Article
ي En
| WPRIM
| ID: wpr-174913
المكتبة المسؤولة:
WPRO
ABSTRACT
OBJECTIVE:
We wanted to compare the human neural stem cell (hNSC) labeling efficacy of different superparamagnetic iron oxide nanoparticles (SPIONs), namely, ferumoxides, monocrystalline iron oxide (MION), cross-linked iron oxide (CLIO)-NH2 and tat-CLIO. MATERIALS ANDMETHODS:
The hNSCs (5x105 HB1F3 cells/ml) were incubated for 24 hr in cell culture media that contained 25 microgram/ml of ferumoxides, MION or CLIO-NH2, and with or without poly-L-lysine (PLL) and tat-CLIO. The cellular iron uptake was analyzed qualitatively with using a light microscope and this was quantified via atomic absorption spectrophotometry. The visibility of the labeled cells was assessed with MR imaging.RESULTS:
The incorporation of SPIONs into the hNSCs did not affect the cellular proliferations and viabilities. The hNSCs labeled with tat-CLIO showed the longest retention, up to 72 hr, and they contained 2.15+/-0.3 pg iron/cell, which are 59 fold, 430 fold and six fold more incorporated iron than that of the hNSCs labeled with ferumoxides, MION or CLIO-NH2, respectively. However, when PLL was added, the incorporation of ferumoxides, MION or CLIO-NH2 into the hNSCs was comparable to that of tat-CLIO.CONCLUSION:
For MR imaging, hNSCs can be efficiently labeled with tat-CLIO alone or with a combination of ferumoxides, MION, CLIO-NH2 and the transfection agent PLL.Key words
النص الكامل:
1
الفهرس:
WPRIM
الموضوع الرئيسي:
Oxides
/
Polylysine
/
Spectrophotometry, Atomic
/
Staining and Labeling
/
Stem Cells
/
Time Factors
/
Magnetic Resonance Imaging
/
Ferric Compounds
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Transfection
/
Gene Products, tat
المحددات:
Humans
اللغة:
En
مجلة:
Korean Journal of Radiology
السنة:
2007
نوع:
Article