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Padfield, K.E., Astrakas, L.G., Zhang, Q., Gopalan, S., Dai, G., Mindrinos, M.N., Tompkins, R.G., Rahme, L.G. and Tzika, A.A. (2005) Burn Injury Causes Mitochondrial Dysfunction in Skeletal Muscle. Proceedings of the National Academy of Sciences of the United States of America, 102, 5368-5373.
https://doi.org/10.1073/pnas.0501211102

has been cited by the following article:

• TITLE: Tracking of Labelled Stem Cells Using Molecular MR Imaging in a Mouse Burn Model in Vivo as an Approach to Regenerative Medicine

  AUTHORS: Zeba Qadri, Valeria Righi, Shasha Li, A. Aria Tzika

  KEYWORDS: Burn Wounds, Cell Labeling, Cell Tracking, Cellular Imaging, Magnetic Resonance, Imaging (MRI), Molecular Imaging, Positive Contrast Imaging, Stem Cells

  JOURNAL NAME: Advances in Molecular Imaging, Vol.11 No.1, January 29, 2021

  ABSTRACT: Therapies based on stem cell transplants offer significant potential in the field of regenerative medicine. Monitoring the fate of the transplanted stem cells in a timely manner is considered one of the main limitations for long-standing success of stem cell transplants. Imaging methods that visualize and track stem cells in vivo non-invasively in real time are helpful towards the development of successful cell transplantation techniques. Novel molecular imaging methods which are non-invasive particularly such as MRI have been of great recent interest. Hence, mouse models which are of clinical relevance have been studied by injecting contrast agents used for labelling cells such as super-paramagnetic iron-oxide (SPIO) nanoparticles for cellular imaging. The MR techniques which can be used to generate positive contrast images have been of much relevance recently for tracking of the labelled cells. Particularly when the off-resonance region in the vicinity of the labeled cells is selectively excited while suppressing the signals from the non-labeled regions by the method of spectral dephasing. Thus, tracking of magnetically labelled cells employing positive contrast in vivo MR imaging methods in a burn mouse model in a non-invasive way has been the scope of this study. The consequences have direct implications for monitoring labeled stem cells at some stage in wound healing. We suggest that our approach can be used in clinical trials in molecular and regenerative medicine.