Purpose: Magnetic resonance imaging (MRI) has been used to track magnetically labeled human bone marrowderived
mesenchymal stem cells (hBMSCs) in vivo after COX-2 silencing and transplantation into nude rats via tail vein
injection. Methods: In the present study, we knocked down COX-2 expression in hBMSCs through lentivirus transduction.
The COX-2 knockdown was confirmed by real-time PCR and Western blotting analyses. Subsequently, we labeled
cells with the novel reagent SPIO-Molday ION Rhodamine-B™ (MIRB). The viability, proliferation and differentiation of
these cells were assessed in vitro. Labeled lenti-shCOX2 hBMSCs, unlabeled hBMSCs and phosphate-buffered saline
(PBS) were individually injected into the tail veins of nude rat models, forming three treatment groups. All nude rats underwent
GRE T2*-weighted MRI at 1 h, 7 days and 14 days post-injection. After MRI examination, the animals were sacrificed,
and the brain and liver were examined by fluorescence microscopy and Prussian Blue staining. Results: Our results
confirmed the successful down-regulation of COX-2 at the mRNA and protein levels in hBMSCs by lentivirus transduction.
The viability and differentiation of hBMSCs were not affected by MIRB labeling. After 7 days, hypointense signal
void areas in the rat livers were observed on MRI. After 14 days, iron particles were detected in the blood vessels, sinusoids,
interlobular septum and capsule tissues of the liver. Conclusion: The MIRB-labeled lenti-shCOX2 hBMSCs
transplanted into nude rat models via tail vein injection can be detected and monitored in vivo using 3.0 T clinical MRI for
up to 14 days after cell transplantation.
COX-2, lentivirus magnetic resonance imaging, mesenchymal stem cells, SPIO transplantation.
Department of Joint Surgery, The Affiliated Hospital of Qingdao University, 59 Haier Rd, 266003, Qingdao, P. R. China.