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Cited 6 time in webofscience Cited 6 time in scopus
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Cell Source-Dependent In Vitro Chondrogenic Differentiation Potential of Mesenchymal Stem Cell Established from Bone Marrow and Synovial Fluid of <i>Camelus dromedarius</i>open access

Authors
Son, Young-BumJeong, Yeon IkJeong, Yeon WooHossein, Mohammad ShamimOlsson, Per OlofTinson, AlexSingh, Kuhad KuldipLee, Sang-YunHwang, Woo Suk
Issue Date
Jul-2021
Publisher
MDPI
Keywords
mesenchymal stem cells; Camelus dromedarius; bone marrow; synovial fluid; chondrocyte differentiation
Citation
ANIMALS, v.11, no.7
Indexed
SCIE
SCOPUS
Journal Title
ANIMALS
Volume
11
Number
7
URI
https://scholarworks.gnu.ac.kr/handle/sw.gnu/72856
DOI
10.3390/ani11071918
ISSN
2076-2615
Abstract
Simple Summary This is the first study to demonstrate the establishment and subsequent analysis of attributes, including the chondrogenic capacity of mesenchymal stem cells (MSCs) from bone marrow (BM) and synovial fluid (SF) from the same donor Camelus dromedarius. MSCs of SF origin were notably more efficient in their chondrogenic capacity and represent a potential source for camel regenerative medicine addressing chondrocyte-related problems. Mesenchymal stem cells (MSCs) are promising multipotent cells with applications for cartilage tissue regeneration in stem cell-based therapies. In cartilage regeneration, both bone marrow (BM-MSCs) and synovial fluid (SF-MSCs) are valuable sources. However, the cellular characteristics and chondrocyte differentiation potential were not reported in either of the camel stem cells. The in vitro chondrocyte differentiation competence of MSCs, from (BM and SF) sources of the same Camelus dromedaries (camel) donor, was determined. Both MSCs were evaluated on pluripotent markers and proliferation capacity. After passage three, both MSCs showed fibroblast-like morphology. The proliferation capacity was significantly increased in SF-MSCs compared to BM-MSCs. Furthermore, SF-MSCs showed an enhanced expression of transcription factors than BM-MSCs. SF-MSCs exhibited lower differentiation potential toward adipocytes than BM-MSCs. However, the osteoblast differentiation potential was similar in MSCs from both sources. Chondrogenic pellets obtained from SF-MSCs revealed higher levels of chondrocyte-specific markers than those from BM-MSCs. Additionally, glycosaminoglycan (GAG) content was elevated in SF-MSCs related to BM-MSCs. This is, to our knowledge, the first study to establish BM-MSCs and SF-MSCs from the same donor and to demonstrate in vitro differentiation potential into chondrocytes in camels.
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