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  •   Ιδρυματικό Αποθετήριο Πανεπιστημίου Θεσσαλίας
  • Επιστημονικές Δημοσιεύσεις Μελών ΠΘ (ΕΔΠΘ)
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ.
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  •   Ιδρυματικό Αποθετήριο Πανεπιστημίου Θεσσαλίας
  • Επιστημονικές Δημοσιεύσεις Μελών ΠΘ (ΕΔΠΘ)
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ.
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Ιδρυματικό Αποθετήριο Πανεπιστημίου Θεσσαλίας
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  • Κοινότητες & Συλλογές
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Proliferative and chondrogenic potential of mesenchymal stromal cells from pluripotent and bone marrow cells

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Συγγραφέας
Sfougataki I., Varela I., Stefanaki K., Karagiannidou A., Roubelakis M.G., Kalodimou V., Papathanasiou I., Traeger-Synodinos J., Kitsiou-Tzeli S., Kanavakis E., Kitra V., Tsezou A., Tzetis M., Goussetis E.
Ημερομηνία
2020
Γλώσσα
en
DOI
10.14670/HH-18-259
Λέξη-κλειδί
biological marker
collagen type 2
SOX9 protein, human
transcription factor Sox9
animal
bone marrow cell
cell differentiation
cell line
cell proliferation
chondrogenesis
comparative study
human
human embryonic stem cell
induced pluripotent stem cell
mesenchymal stem cell
metabolism
nonobese diabetic mouse
phenotype
physiology
SCID mouse
signal transduction
Animals
Biomarkers
Bone Marrow Cells
Cell Differentiation
Cell Line
Cell Proliferation
Chondrogenesis
Collagen Type II
Human Embryonic Stem Cells
Humans
Induced Pluripotent Stem Cells
Mesenchymal Stem Cells
Mice, Inbred NOD
Mice, SCID
Phenotype
Signal Transduction
SOX9 Transcription Factor
Histology and Histopathology
Εμφάνιση Μεταδεδομένων
Επιτομή
Summary. Introduction. Mesenchymal stromal cells (MSCs) can be derived from a wide range of fetal and adult sources including pluripotent stem cells (PSCs). The properties of PSC-derived MSCs need to be fully characterized, in order to evaluate the feasibility of their use in clinical applications. PSC-MSC proliferation and differentiation potential in comparison with bone marrow (BM)-MSCs is still under investigation. The objective of this study was to determine the proliferative and chondrogenic capabilities of both human induced pluripotent stem cell (hiPSC-) and embryonic stem cell (hESC-) derived MSCs, by comparing them with BMMSCs. Methods. MSCs were derived from two hiPSC lines (hiPSC-MSCs), the well characterized Hues9 hESC line (hESC-MSCs) and BM from two healthy donors (BMMSCs). Proliferation potential was investigated using appropriate culture conditions, with serial passaging, until cells entered into senescence. Differentiation potential to cartilage was examined after in vitro chondrogenic culture conditions. Results. BM-MSCs revealed a fold expansion of 1.18x105 and 2.3x105 while the two hiPSC-MSC lines and hESC-MSC showed 5.88x1010, 3.49x108 and 2.88x108, respectively. Under chondrogenic conditions, all MSC lines showed a degree of chondrogenesis. However, when we examined the formed chondrocyte micromasses by histological analysis of the cartilage morphology and immunohistochemistry for the chondrocyte specific markers Sox9 and Collagen II, we observed that PSC-derived MSC lines had formed pink rather than hyaline cartilage, in contrast to BM-MSCs. Conclusion. In conclusion, MSCs derived from both hESCs and hiPSCs had superior proliferative capacity compared to BM-MSCs, but they were inefficient in their ability to form hyaline cartilage. © 2020, Histology and Histopathology. All rights reserved.
URI
http://hdl.handle.net/11615/78909
Collections
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ. [19743]

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