Rabbit mesenchymal stem cells cultured in a dynamic culture system displayed superior cell proliferation and osteogenetic induction

Ching Li Tseng, King Ming Chang, Chi Chang Wu, Yang Kao Wang, Ing Kae Wang

研究成果: Article

2 引文 (Scopus)

摘要

Objective: We evaluated the effect of three-dimensional static and dynamic culture on the proliferation, distribution, and differentiation of rabbit mesenchymal stem cells (MSCs) in a porous scaffold via autograft for bone regeneration. Methods: Rabbit MSCs were seeded in a porous hydroxyapatite scaffold (MSCs/scaffold), and then cultured in petri dishes and a bidirectional flow reactor for 4 weeks for osteogenetic induction invitro. Metabolic assay of the culture medium was carried out every 2 days; glucose, lactic acid, and calcium concentrations in the medium were also examined. Cell distribution in the scaffold was examined histologically. Cultured MSCs/scaffolds were implanted in rabbit condyles for the evaluation of bone regeneration invivo. Results: Histological sections showed that cells cultured in petri dishes grew only around the scaffolds and seldom in the inner part. However, the scaffolds cultured with MSCs in a bioreactor were almost fully occupied by cells. Metabolic results revealed that the average concentration of glucose in the medium was decreased as cells propagated. Glucose consumption was observed in both static and dynamic cultures, but higher lactic acid production was found in the static culture. Calcium ion concentration was reduced significantly in the dynamic culture after the addition of an osteogenetic induction medium, indicating progression of mineralization. The invivo results showed that about 80% of the defect in the condyles with dynamically cultured MSCs/scaffold implants was filled with new bone tissue, a proportion much higher than that in the petri dish-cultured MSCs/scaffolds, in which only half of the bone regeneration occurred in the cavity. Conclusion: This study provides evidence of the effectiveness of dynamic invitro MSC culture for robust osteogenesis and indicates that it may impart superior potential for bone regeneration invivo.

原文English
頁(從 - 到)10-15
頁數6
期刊Journal of Experimental and Clinical Medicine(Taiwan)
6
發行號1
DOIs
出版狀態Published - 2014 二月 1

指紋

Mesenchymal Stromal Cells
Cell Proliferation
Rabbits
Bone Regeneration
Bone and Bones
Glucose
Lactic Acid
Calcium Carbonate
Autografts
Bioreactors
Durapatite
Osteogenesis
Culture Media
Cultured Cells
Cell Culture Techniques
Ions
Calcium

All Science Journal Classification (ASJC) codes

  • Medicine(all)

引用此文

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abstract = "Objective: We evaluated the effect of three-dimensional static and dynamic culture on the proliferation, distribution, and differentiation of rabbit mesenchymal stem cells (MSCs) in a porous scaffold via autograft for bone regeneration. Methods: Rabbit MSCs were seeded in a porous hydroxyapatite scaffold (MSCs/scaffold), and then cultured in petri dishes and a bidirectional flow reactor for 4 weeks for osteogenetic induction invitro. Metabolic assay of the culture medium was carried out every 2 days; glucose, lactic acid, and calcium concentrations in the medium were also examined. Cell distribution in the scaffold was examined histologically. Cultured MSCs/scaffolds were implanted in rabbit condyles for the evaluation of bone regeneration invivo. Results: Histological sections showed that cells cultured in petri dishes grew only around the scaffolds and seldom in the inner part. However, the scaffolds cultured with MSCs in a bioreactor were almost fully occupied by cells. Metabolic results revealed that the average concentration of glucose in the medium was decreased as cells propagated. Glucose consumption was observed in both static and dynamic cultures, but higher lactic acid production was found in the static culture. Calcium ion concentration was reduced significantly in the dynamic culture after the addition of an osteogenetic induction medium, indicating progression of mineralization. The invivo results showed that about 80{\%} of the defect in the condyles with dynamically cultured MSCs/scaffold implants was filled with new bone tissue, a proportion much higher than that in the petri dish-cultured MSCs/scaffolds, in which only half of the bone regeneration occurred in the cavity. Conclusion: This study provides evidence of the effectiveness of dynamic invitro MSC culture for robust osteogenesis and indicates that it may impart superior potential for bone regeneration invivo.",
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Rabbit mesenchymal stem cells cultured in a dynamic culture system displayed superior cell proliferation and osteogenetic induction. / Tseng, Ching Li; Chang, King Ming; Wu, Chi Chang; Wang, Yang Kao; Wang, Ing Kae.

於: Journal of Experimental and Clinical Medicine(Taiwan), 卷 6, 編號 1, 01.02.2014, p. 10-15.

研究成果: Article

TY - JOUR

T1 - Rabbit mesenchymal stem cells cultured in a dynamic culture system displayed superior cell proliferation and osteogenetic induction

AU - Tseng, Ching Li

AU - Chang, King Ming

AU - Wu, Chi Chang

AU - Wang, Yang Kao

AU - Wang, Ing Kae

PY - 2014/2/1

Y1 - 2014/2/1

N2 - Objective: We evaluated the effect of three-dimensional static and dynamic culture on the proliferation, distribution, and differentiation of rabbit mesenchymal stem cells (MSCs) in a porous scaffold via autograft for bone regeneration. Methods: Rabbit MSCs were seeded in a porous hydroxyapatite scaffold (MSCs/scaffold), and then cultured in petri dishes and a bidirectional flow reactor for 4 weeks for osteogenetic induction invitro. Metabolic assay of the culture medium was carried out every 2 days; glucose, lactic acid, and calcium concentrations in the medium were also examined. Cell distribution in the scaffold was examined histologically. Cultured MSCs/scaffolds were implanted in rabbit condyles for the evaluation of bone regeneration invivo. Results: Histological sections showed that cells cultured in petri dishes grew only around the scaffolds and seldom in the inner part. However, the scaffolds cultured with MSCs in a bioreactor were almost fully occupied by cells. Metabolic results revealed that the average concentration of glucose in the medium was decreased as cells propagated. Glucose consumption was observed in both static and dynamic cultures, but higher lactic acid production was found in the static culture. Calcium ion concentration was reduced significantly in the dynamic culture after the addition of an osteogenetic induction medium, indicating progression of mineralization. The invivo results showed that about 80% of the defect in the condyles with dynamically cultured MSCs/scaffold implants was filled with new bone tissue, a proportion much higher than that in the petri dish-cultured MSCs/scaffolds, in which only half of the bone regeneration occurred in the cavity. Conclusion: This study provides evidence of the effectiveness of dynamic invitro MSC culture for robust osteogenesis and indicates that it may impart superior potential for bone regeneration invivo.

AB - Objective: We evaluated the effect of three-dimensional static and dynamic culture on the proliferation, distribution, and differentiation of rabbit mesenchymal stem cells (MSCs) in a porous scaffold via autograft for bone regeneration. Methods: Rabbit MSCs were seeded in a porous hydroxyapatite scaffold (MSCs/scaffold), and then cultured in petri dishes and a bidirectional flow reactor for 4 weeks for osteogenetic induction invitro. Metabolic assay of the culture medium was carried out every 2 days; glucose, lactic acid, and calcium concentrations in the medium were also examined. Cell distribution in the scaffold was examined histologically. Cultured MSCs/scaffolds were implanted in rabbit condyles for the evaluation of bone regeneration invivo. Results: Histological sections showed that cells cultured in petri dishes grew only around the scaffolds and seldom in the inner part. However, the scaffolds cultured with MSCs in a bioreactor were almost fully occupied by cells. Metabolic results revealed that the average concentration of glucose in the medium was decreased as cells propagated. Glucose consumption was observed in both static and dynamic cultures, but higher lactic acid production was found in the static culture. Calcium ion concentration was reduced significantly in the dynamic culture after the addition of an osteogenetic induction medium, indicating progression of mineralization. The invivo results showed that about 80% of the defect in the condyles with dynamically cultured MSCs/scaffold implants was filled with new bone tissue, a proportion much higher than that in the petri dish-cultured MSCs/scaffolds, in which only half of the bone regeneration occurred in the cavity. Conclusion: This study provides evidence of the effectiveness of dynamic invitro MSC culture for robust osteogenesis and indicates that it may impart superior potential for bone regeneration invivo.

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