Long-term and label-free monitoring for osteogenic differentiation of mesenchymal stem cells using force sensor and impedance measurement

2020 ◽  
Vol 8 (43) ◽  
pp. 9913-9920
Author(s):  
Zhizhong Zhang ◽  
Tianyang Zheng ◽  
Rong Zhu

Label-free and continuous multimodal measurements of cell traction force and cell impedance for studying osteogenic differentiation of stem cells.

2021 ◽  
Author(s):  
Ebrahim Rahmani-Moghadam ◽  
Tahereh Talaei-Khozani ◽  
Vahideh Zarrin ◽  
Zahra Vojdani

Abstract Background: Hydroxyapatite (HA) can be loaded by some osteogenic inducing agents such as thymoquinone (TQ) and alginate. This study was performed to investigate the effect of TQ loading into HA/alginate scaffolds on osteogenic differentiation capability of mesenchymal stem cells.Methods: HA scaffolds were fabricated by casting and sintering method and impregnated by TQ containing alginate. The stem cells were loaded onto the scaffolds and induced to differentiate into osteoblasts. Alkaline Phosphatase (ALP) activity, Alizarin Red S, Real-Time qRT-PCR, and MTT assessments were done. Finally, the cells were examined with a light microscope, confocal microscope, and SEM.Results: The results showed that the presence of the alginate decelerates the degradation rate and reinforces the mechanical strength. while the presence of TQ had no significant influence on physical and mechanical properties of the HA/alginate scaffolds, it led to a significant increase in ALP activity and expression of collagen, osteopontin, and osteocalcin at early phase of differentiation. Also, TQ administration had no impact on calcium deposition and proliferation as well as bone-marker expression at long term differentiation.Conclusion: TQ accelerates the differentiation of the stem cells into the osteoblasts without changing the properties of the scaffolds, and the HA/alginate/TQ scaffold can be used as a scaffold with osteogenic properties in bone tissue engineering applications.


Author(s):  
Sepanta Hosseinpour ◽  
Yuxue Cao ◽  
Jingyu Liu ◽  
Chun Xu ◽  
Laurence J. Walsh

Surface functionalized MSNs with large radial pores delivered miRNA-26a-5p into rat bone marrow mesenchymal stem cells and promote their osteogenic differentiation. Lyophilized dry powder formulation remained functional after 6 months of storage.


RSC Advances ◽  
2016 ◽  
Vol 6 (66) ◽  
pp. 61771-61776 ◽  
Author(s):  
Yu Gao ◽  
Chenjie Xu ◽  
Lianhui Wang

Raman imaging allows the non-invasive and label-free monitoring of the preferred osteogenic differentiation of human mesenchymal stem cells on the polycaprolactone scaffolds.


Blood ◽  
2007 ◽  
Vol 110 (11) ◽  
pp. 4066-4066
Author(s):  
Xiaoyan Zhang ◽  
Jianyong Li ◽  
Yujie Wu ◽  
Jun Xia ◽  
Yaping Zhang ◽  
...  

Abstract Background Mesenchymal stem cells (MSCs) are now used in repair medicine and transplantation because of its multipotency and immunomodulatory effect. They need in vitro expansion to get adequate number for clinical use. Human MSCs had been observed to enter senescence during in vitro culture. We evaluated that the same phenomenon existed during long term culture of rat MSCs. Methods Bone marrow from ten male Sprague-Dawley (SD) rats (198±2.12g) were cultured and nonadherent cells were removed three days later. MSCs were identified by osteogenic differentiation and adipocytic differentiation. Cells of each passage were detected for morphology by Wright’s staining, ultrastructure by scanning electron microscope, growth curve by CCK-8 kits detection, osteogenic differentiation and von kossa staining, adipocytic differentiation and oil red staining, βgalactosidase staining, quantitative assay of p16INK4a gene. Results Rat MSCs were Fusiform shaped or polygon. Cells were becoming flatter and bigger during passaging. More swelling endoplasmic reticulum and demyelinate mitochondrion were observed by scanning electron microscope during passaging. The proliferation of the cells slowed from the 6th passage and stopped at the 8th or 9th passage. The positive rate of βgalactosidase staining and p16INK4a gene increased in cells after 5th passage. Osteogenic and adipocytic potential were attenuated in cells after 6th passage. Conclusions MSCs enter senescence during long term culture. Their potential of proliferation and multipotency dropped.


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