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涂覆有合成骨靶向聚合物的间充质干细胞可增强骨质疏松性骨折的再生能力。

Mesenchymal Stem Cells Coated with Synthetic Bone-Targeting Polymers Enhance Osteoporotic Bone Fracture Regeneration.

作者信息

Safarova Yantsen Yuliya, Olzhayev Farkhad, Umbayev Bauyrzhan, Tsoy Andrey, Hortelano Gonzalo, Tokay Tursonjan, Murata Hironobu, Russell Alan, Askarova Sholpan

机构信息

Laboratory of Bioengineering and Regenerative Medicine, National Laboratory Astana, Nazarbayev University, Nur-Sultan 010000, Kazakhstan.

School of Engineering and Digital Sciences, Nazarbayev University, Nur-Sultan 010000, Kazakhstan.

出版信息

Bioengineering (Basel). 2020 Oct 12;7(4):125. doi: 10.3390/bioengineering7040125.

DOI:10.3390/bioengineering7040125
PMID:33053753
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7711537/
Abstract

Osteoporosis is a progressive skeletal disease characterized by reduced bone density leading to bone fragility and an elevated risk of bone fractures. In osteoporotic conditions, decrease in bone density happens due to the augmented osteoclastic activity and the reduced number of osteoblast progenitor cells (mesenchymal stem cells, MSCs). We investigated a new method of cell therapy with membrane-engineered MSCs to restore the osteoblast progenitor pool and to inhibit osteoclastic activity in the fractured osteoporotic bones. The primary active sites of the polymer are the N-hydroxysuccinimide and bisphosphonate groups that allow the polymer to covalently bind to the MSCs' plasma membrane, target hydroxyapatite molecules on the bone surface and inhibit osteolysis. The therapeutic utility of the membrane-engineered MSCs was investigated in female rats with induced estrogen-dependent osteoporosis and ulnar fractures. The analysis of the bone density dynamics showed a 27.4% and 21.5% increase in bone density at 4 and 24 weeks after the osteotomy of the ulna in animals that received four transplantations of polymer-modified MSCs. The results of the intravital observations were confirmed by the post-mortem analysis of histological slices of the fracture zones. Therefore, this combined approach that involves polymer and cell transplantation shows promise and warrants further bio-safety and clinical exploration.

摘要

骨质疏松症是一种进行性骨骼疾病,其特征是骨密度降低,导致骨骼脆弱,骨折风险升高。在骨质疏松症状态下,骨密度降低是由于破骨细胞活性增强和成骨祖细胞(间充质干细胞,MSCs)数量减少所致。我们研究了一种用膜工程化间充质干细胞进行细胞治疗的新方法,以恢复成骨祖细胞池并抑制骨折骨质疏松骨中的破骨细胞活性。聚合物的主要活性位点是N-羟基琥珀酰亚胺和双膦酸盐基团,它们使聚合物能够与间充质干细胞的质膜共价结合,靶向骨表面的羟基磷灰石分子并抑制骨溶解。在诱导雌激素依赖性骨质疏松症和尺骨骨折的雌性大鼠中研究了膜工程化间充质干细胞的治疗效用。骨密度动态分析显示,接受聚合物修饰间充质干细胞四次移植的动物在尺骨截骨术后4周和24周时骨密度分别增加了27.4%和21.5%。活体观察结果通过骨折区域组织切片的死后分析得到证实。因此,这种涉及聚合物和细胞移植的联合方法显示出前景,值得进一步进行生物安全性和临床探索。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f2df/7711537/fc240f991fbf/bioengineering-07-00125-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f2df/7711537/7bbf893d1d74/bioengineering-07-00125-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f2df/7711537/af3f1e20bc7d/bioengineering-07-00125-g002.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f2df/7711537/c1c99ea9ab75/bioengineering-07-00125-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f2df/7711537/051a6508f8f3/bioengineering-07-00125-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f2df/7711537/64d304dfd59f/bioengineering-07-00125-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f2df/7711537/a4f1e13a1ff0/bioengineering-07-00125-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f2df/7711537/fc240f991fbf/bioengineering-07-00125-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f2df/7711537/7bbf893d1d74/bioengineering-07-00125-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f2df/7711537/af3f1e20bc7d/bioengineering-07-00125-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f2df/7711537/d4d3d20ee9ca/bioengineering-07-00125-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f2df/7711537/c1c99ea9ab75/bioengineering-07-00125-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f2df/7711537/051a6508f8f3/bioengineering-07-00125-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f2df/7711537/64d304dfd59f/bioengineering-07-00125-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f2df/7711537/a4f1e13a1ff0/bioengineering-07-00125-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f2df/7711537/fc240f991fbf/bioengineering-07-00125-g008.jpg

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本文引用的文献

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