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Comparison of morphology, protein concentration, and size distribution of bone marrow and Wharton's jelly-derived mesenchymal stem cells exosomes isolated by ultracentrifugation and polymer-based precipitation techniques.
Rahmatinejad, Fatemeh; Kharat, Zahra; Jalili, Hasan; Renani, Mahboubeh Kabiri; Mobasheri, Hamid.
Affiliation
  • Rahmatinejad F; Department of Life Science Engineering, Faculty of New Sciences & Technologies, University of Tehran, Tehran, Iran.
  • Kharat Z; Department of Biotechnology, College of Science, University of Tehran, Tehran, Iran.
  • Jalili H; Department of Life Science Engineering, Faculty of New Sciences & Technologies, University of Tehran, Tehran, Iran. Electronic address: Hjalili@ut.ac.ir.
  • Renani MK; Department of Biotechnology, College of Science, University of Tehran, Tehran, Iran. Electronic address: mkabiri@ut.ac.ir.
  • Mobasheri H; Institute of Biochemistry and Biophysics, University of Tehran, Tehran, Iran.
Tissue Cell ; 88: 102427, 2024 Jun.
Article in En | MEDLINE | ID: mdl-38833940
ABSTRACT
Exosomes which are tiny extracellular vesicles (30-150 nm), transport vital proteins and gene materials such as miRNA, mRNA, or DNA, whose role in cell communication and epithelia regulation is critical. Many techniques have been developed as a result of studying exosomes' biochemical and physicochemical properties, although there is still no standard method to isolate exosomes simply with high yield. Commercial kits have gained popularity for exosome extraction despite concerns about their effectiveness in scientific research. On the other hand, ultracentrifugation remains the gold standard isolation method. This study compares these two common exosome isolation methods to determine their impact on the quality and quantity of exosomes isolated from bone marrow (BM) and Wharton's jelly (WJ)-derived mesenchymal stem cells. Isolated exosomes from the two sources of the cell's conditioned medium by two methods (polymer kit and ultracentrifuge) were characterized using western blotting, scanning electron microscopy (SEM), dynamic light scattering (DLS), and the Bradford assay. Western blot analysis confirmed separation efficiency based on CD81 and CD63 markers, with the absence of calnexin serving as a negative control. The Morphology of exosomes studied by SEM image analysis revealed a similar round shape appearance and their sizes (30-150 nm) were the same in both isolation techniques. The DLS analysis of the sample results was consistent with the SEM ones, showing a similar size range and very low disparity. The exosome protein content concentration analysis revealed that exosomes isolated by the polymer-based kits contained higher protein concentration density and purity (p <0.001). In general, though the protein yield was higher when the polymer-based kits were used, there were no significant differences in morphology, or size between WJ-derived and BM-derived exosomes, regardless of the isolation method employed.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Ultracentrifugation / Bone Marrow Cells / Exosomes / Wharton Jelly / Mesenchymal Stem Cells Limits: Humans Language: En Journal: Tissue Cell Year: 2024 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Ultracentrifugation / Bone Marrow Cells / Exosomes / Wharton Jelly / Mesenchymal Stem Cells Limits: Humans Language: En Journal: Tissue Cell Year: 2024 Document type: Article