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人脂肪组织来源间充质干细胞(hATMSCs)在裸鼠股骨节段性缺损模型中的疗效和安全性评估的确立。

Establishment of efficacy and safety assessment of human adipose tissue-derived mesenchymal stem cells (hATMSCs) in a nude rat femoral segmental defect model.

机构信息

Graduate School of Immunology, Seoul National University College of Medicine, Seoul, Korea.

出版信息

J Korean Med Sci. 2011 Apr;26(4):482-91. doi: 10.3346/jkms.2011.26.4.482. Epub 2011 Mar 28.


DOI:10.3346/jkms.2011.26.4.482
PMID:21468254
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3069566/
Abstract

Human adipose tissue-derived mesenchymal stem cell (hATMSC) have emerged as a potentially powerful tool for bone repair, but an appropriate evaluation system has not been established. The purpose of this study was to establish a preclinical assessment system to evaluate the efficacy and safety of cell therapies in a nude rat bone defect model. Segmental defects (5 mm) were created in the femoral diaphyses and transplanted with cell media (control), hydroxyapatite/tricalcium phosphate scaffolds (HA/TCP, Group I), hATMSCs (Group II), or three cell-loading density of hATMSC-loaded HA/TCP (Group III-V). Healing response was evaluated by serial radiography, micro-computed tomography and histology at 16 weeks. To address safety-concerns, we conducted a GLP-compliant toxicity study. Scanning electron microscopy studies showed that hATMSCs filled the pores/surfaces of scaffolds in a cell-loading density-dependent manner. We detected significant increases in bone formation in the hATMSC-loaded HA/TCP groups compared with other groups. The amount of new bone formation increased with increases in loaded cell number. In a toxicity study, no significant hATMSC-related changes were found in body weights, clinical signs, hematological/biochemical values, organ weights, or histopathological findings. In conclusion, hATMSCs loaded on HA/TCP enhance the repair of bone defects and was found to be safe under our preclinical efficacy/safety hybrid assessment system.

摘要

人脂肪组织来源的间充质干细胞(hATMSC)已成为骨修复的潜在有力工具,但尚未建立适当的评估系统。本研究旨在建立一种临床前评估系统,以评估细胞疗法在裸鼠骨缺损模型中的疗效和安全性。在股骨骨干中创建节段性缺损(5mm),并用细胞培养基(对照)、羟基磷灰石/磷酸三钙支架(HA/TCP,I 组)、hATMSC(II 组)或三种细胞负载密度的 hATMSC 负载 HA/TCP(III-V 组)进行移植。在 16 周时通过连续放射照相、微计算机断层扫描和组织学评估愈合反应。为了解决安全性问题,我们进行了符合 GLP 标准的毒性研究。扫描电子显微镜研究表明,hATMSC 以细胞负载密度依赖的方式填充支架的孔/表面。与其他组相比,负载 hATMSC 的 HA/TCP 组的骨形成明显增加。随着加载细胞数量的增加,新骨形成的量也增加。在毒性研究中,在体重、临床症状、血液学/生化值、器官重量或组织病理学发现方面,均未发现与 hATMSC 相关的显著变化。总之,负载在 HA/TCP 上的 hATMSC 增强了骨缺损的修复,并且在我们的临床前疗效/安全性混合评估系统下被发现是安全的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2019/3069566/204163b5a7d7/jkms-26-482-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2019/3069566/fc22bcf79f12/jkms-26-482-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2019/3069566/08841307c17a/jkms-26-482-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2019/3069566/0f50d018f39c/jkms-26-482-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2019/3069566/43e5666887e0/jkms-26-482-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2019/3069566/e3bf3321801f/jkms-26-482-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2019/3069566/204163b5a7d7/jkms-26-482-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2019/3069566/fc22bcf79f12/jkms-26-482-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2019/3069566/08841307c17a/jkms-26-482-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2019/3069566/0f50d018f39c/jkms-26-482-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2019/3069566/43e5666887e0/jkms-26-482-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2019/3069566/e3bf3321801f/jkms-26-482-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2019/3069566/204163b5a7d7/jkms-26-482-g006.jpg

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本文引用的文献

[1]
Development of sarcomas in mice implanted with mesenchymal stem cells seeded onto bioscaffolds.

Carcinogenesis. 2009-1

[2]
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Biomaterials. 2008-1

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J Vet Med Sci. 2007-8

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Bone healing and migration of cord blood-derived stem cells into a critical size femoral defect after xenotransplantation.

J Bone Miner Res. 2007-8

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Stem Cells. 2007-6

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Tissue Eng. 2006-6

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Allogenic peripheral blood derived mesenchymal stem cells (MSCs) enhance bone regeneration in rabbit ulna critical-sized bone defect model.

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