Tuba Zendehboudi
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Tuba Zendehboudi has a total of 23 co-authors. Here are the top co-authors by number of shared publications:
- Alireza Afshar
Department of Public Health and Public Health Care, West-Kazakhstan Marat Ospanov Medical University
2 shared publications - Amin Tamadon
Department of Natural Sciences, West Kazakhstan Marat Ospanov Medical University, Aktobe 030019, Kazakhstan
2 shared publications - Akmaral Baspakova
Department of Epidemiology, West Kazakhstan Marat Ospanov Medical University, Aktobe, Kazakhstan
1 shared publication - Alireza Barmak
Food Lab, Bushehr University of Medical Sciences, Bushehr 75, Iran
1 shared publication - Alireza Hashemi
Apple Inc, Seattle, United States
1 shared publication - Arezoo Khoradmehr
Persian Gulf Marine Biotechnology Research Sciences Center, The Persian Gulf Biomedical Research Sciences Institute, Bushehr University of Medical Sciences, Bushehr, 75147, Iran, bpums.ac.ir
1 shared publication
Latest Publications
- Open Access
- 13 February 2023
- Published by MDPI AG in Biosensors
- Vol. 13 (2) , 268
MRI Tracking of Marine Proliferating Cells In Vivo Using Anti-Oct4 Antibody-Conjugated Iron Nanoparticles for Precision in Regenerative Medicine
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.
- 13 February 2023
- Published by MDPI AG in Biosensors
- Vol. 13 (2) , 268
Open AccessMRI Tracking of Marine Proliferating Cells In Vivo Using Anti-Oct4 Antibody-Conjugated Iron Nanoparticles for Precision in Regenerative Medicine
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.
- Open Access
- 16 December 2022
- Published by Springer Nature in Wetlands Ecology and Management
- Vol. 31 (1) , 115-128
Reforestation of grey mangroves (Avicennia marina) along the northern coasts of the Persian Gulf
- 16 December 2022
- Published by Springer Nature in Wetlands Ecology and Management
- Vol. 31 (1) , 115-128
Open AccessReforestation of grey mangroves (Avicennia marina) along the northern coasts of the Persian Gulf