MRI Tracking of Marine Proliferating Cells In Vivo Using Anti-Oct4 Antibody-Conjugated Iron Nanoparticles for Precision in Regenerative Medicine

• Published in: Biosensors (Basel) Vol. 13; no. 2; p. 268
• Main Authors: Baghban, Neda, Khoradmehr, Arezoo, Afshar, Alireza, Jafari, Nazanin, Zendehboudi, Tuba, Rasekh, Poorya, Abolfathi, Leila Gholamian, Barmak, Alireza, Mohebbi, Gholamhossein, Akmaral, Baspakova, Askerovich, Kaliyev Asset, Maratovich, Mussin Nadiar, Azari, Hossein, Assadi, Majid, Nabipour, Iraj, Tamadon, Amin
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 01.02.2023; MDPI
• Subjects: Affinity; Analysis; Antibodies; Blue stain; Cell culture; Cell growth; Cell proliferation; Cell surface; Fluorescence; Health aspects; In vivo methods and tests; Invertebrates; Iron; Laboratory animals; magnetic nanoparticle; Magnetic resonance imaging; marine; Marine environment; Marine invertebrates; Medical research; Mesenchyme; Methods; MRI; Nanoparticles; Oct-4 protein; Pigments; Quantum dots; Regenerative medicine; Saline water; Seawater; Stem cells; Surface markers; Tomography; Tracking; Vertebrates; Iran; magnetic nanoparticle; cell proliferation; MRI; tracking; marine
• ISSN: 2079-6374; 2079-6374
• DOI: 10.3390/bios13020268

Marine invertebrates are multicellular organisms consisting of a wide range of marine environmental species. Unlike vertebrates, including humans, one of the challenges in identifying and tracking invertebrate stem cells is the lack of a specific marker. Labeling stem cells with magnetic particles provides a non-invasive, in vivo tracking method using MRI. This study suggests antibody-conjugated iron nanoparticles (NPs), which are detectable with MRI for in vivo tracking, to detect stem cell proliferation using the Oct4 receptor as a marker of stem cells. In the first phase, iron NPs were fabricated, and their successful synthesis was confirmed using FTIR spectroscopy. Next, the Alexa Fluor anti-Oct4 antibody was conjugated with as-synthesized NPs. Their affinity to the cell surface marker in fresh and saltwater conditions was confirmed using two types of cells, murine mesenchymal stromal/stem cell culture and sea anemone stem cells. For this purpose, 106 cells of each type were exposed to NP-conjugated antibodies and their affinity to antibodies was confirmed by an epi-fluorescent microscope. The presence of iron-NPs imaged with the light microscope was confirmed by iron staining using Prussian blue stain. Next, anti-Oct4 antibodies conjugated with iron NPs were injected into a brittle star, and proliferating cells were tracked by MRI. To sum up, anti-Oct4 antibodies conjugated with iron NPs not only have the potential for identifying proliferating stem cells in different cell culture conditions of sea anemone and mouse cell cultures but also has the potential to be used for in vivo MRI tracking of marine proliferating cells.