Mesenchymal stem cells (MSCs) have demonstrated great potential for tissue engineering and regenerative medicine applications. Noninvasive and real-term tracking of transplanted MSCs in vivo is crucial for studying the distribution and migration of MSCs, and their role in tissue injury repair. This study reports on the use of ferrimagnetic vortex iron oxide (FVIO) nanorings modified with anti-human integrin β 1 for specific recognition and magnetic resonance imaging (MRI) tracking of human MSCs (hMSCs). Integrin β 1 is highly expressed at all stem cell proliferation and differentiation stages. Therefore, the anti-integrin β 1 antibody (Ab) introduced in FVIO targets integrin β 1, thus enabling FVIO to target stem cells at any stage. This is unlike the traditional MRI-based monitoring of transplanted stem cells, which usually requires pre-labeling the stem cells with tracers before injection. Because of the ability to recognize hMSCs, the Ab-modified FVIO nanotracers (FVIO-Ab) have the advantage of not requiring pre-labeling before stem cell transplantation. Furthermore, the FVIO-Ab nanotracers have high T * ₂ contrast resulting from the unique magnetic properties of FVIO which can improve the MRI tracking efficiency of stem cells. This work may provide a new way for stem cell labeling and in vivo MRI tracking, thus reducing the risks associated with stem cell transplantation and promoting clinical translation.
Keyphrases
- stem cells
- mesenchymal stem cells
- stem cell transplantation
- magnetic resonance imaging
- contrast enhanced
- umbilical cord
- endothelial cells
- high dose
- cell therapy
- diffusion weighted imaging
- iron oxide
- cell proliferation
- magnetic resonance
- bone marrow
- induced pluripotent stem cells
- computed tomography
- tissue engineering
- emergency department
- climate change
- risk assessment
- signaling pathway
- drug delivery
- human health
- molecularly imprinted
- pi k akt
- simultaneous determination