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本文引用的文献

1
Encapsulated dental-derived mesenchymal stem cells in an injectable and biodegradable scaffold for applications in bone tissue engineering.包被在可注射可生物降解支架中的牙齿来源间充质干细胞在骨组织工程中的应用。
J Biomed Mater Res A. 2013 Nov;101(11):3285-94. doi: 10.1002/jbm.a.34546. Epub 2013 Aug 24.
2
The combined use of cell sheet fragments of periodontal ligament stem cells and platelet-rich fibrin granules for avulsed tooth reimplantation.牙周膜干细胞细胞片碎片与富血小板纤维蛋白颗粒联合用于牙脱位再植。
Biomaterials. 2013 Jul;34(22):5506-20. doi: 10.1016/j.biomaterials.2013.03.079. Epub 2013 Apr 29.
3
Angiogenic and osteogenic potential of platelet-rich plasma and adipose-derived stem cell laden alginate microspheres.富含血小板血浆和负载藻酸盐微球的脂肪来源干细胞的血管生成和成骨潜力。
Biomaterials. 2012 Dec;33(34):8802-11. doi: 10.1016/j.biomaterials.2012.08.054. Epub 2012 Sep 12.
4
Alginate hydrogel as a promising scaffold for dental-derived stem cells: an in vitro study.藻酸盐水凝胶作为一种有前途的牙齿来源干细胞支架:一项体外研究。
J Mater Sci Mater Med. 2012 Dec;23(12):3041-51. doi: 10.1007/s10856-012-4759-3. Epub 2012 Sep 4.
5
Bone repair using periodontal ligament progenitor cell-seeded constructs.使用牙周韧带祖细胞种植构建体进行骨修复。
J Dent Res. 2012 Aug;91(8):789-94. doi: 10.1177/0022034512452430. Epub 2012 Jun 26.
6
Mesenchymal stem cell-based tissue regeneration is governed by recipient T lymphocytes via IFN-γ and TNF-α.基于间充质干细胞的组织再生受受体 T 淋巴细胞通过 IFN-γ 和 TNF-α 调控。
Nat Med. 2011 Nov 20;17(12):1594-601. doi: 10.1038/nm.2542.
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A highly organized three-dimensional alginate scaffold for cartilage tissue engineering prepared by microfluidic technology.采用微流控技术制备的高度有序的三维藻酸盐软骨组织工程支架。
Biomaterials. 2011 Oct;32(29):7118-26. doi: 10.1016/j.biomaterials.2011.06.018. Epub 2011 Jul 2.
8
Engineered alginate hydrogels for effective microfluidic capture and release of endothelial progenitor cells from whole blood.用于有效从全血中捕获和释放内皮祖细胞的工程化藻酸盐水凝胶。
Langmuir. 2011 Apr 5;27(7):4257-64. doi: 10.1021/la105016a. Epub 2011 Mar 14.
9
Gingiva-derived mesenchymal stem cell-mediated therapeutic approach for bone tissue regeneration.牙龈间充质干细胞介导的骨组织再生治疗方法。
Stem Cells Dev. 2011 Dec;20(12):2093-102. doi: 10.1089/scd.2010.0523. Epub 2011 Apr 27.
10
Strategies for regeneration of the bone using porcine adult adipose-derived mesenchymal stem cells.利用猪成年脂肪来源间充质干细胞促进骨再生的策略。
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包被在 RGD 修饰的藻酸盐支架中的牙周韧带或牙龈组织来源的干细胞的骨再生潜力。

Bone regeneration potential of stem cells derived from periodontal ligament or gingival tissue sources encapsulated in RGD-modified alginate scaffold.

机构信息

1 Center for Craniofacial and Molecular Biology (CCMB), Ostrow School of Dentistry, University of Southern California , Los Angeles, California.

出版信息

Tissue Eng Part A. 2014 Feb;20(3-4):611-21. doi: 10.1089/ten.TEA.2013.0229. Epub 2013 Nov 6.

DOI:10.1089/ten.TEA.2013.0229
PMID:24070211
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3926152/
Abstract

Mesenchymal stem cells (MSCs) provide an advantageous alternative therapeutic option for bone regeneration in comparison to current treatment modalities. However, delivering MSCs to the defect site while maintaining a high MSC survival rate is still a critical challenge in MSC-mediated bone regeneration. Here, we tested the bone regeneration capacity of periodontal ligament stem cells (PDLSCs) and gingival mesenchymal stem cells (GMSCs) encapsulated in a novel RGD- (arginine-glycine-aspartic acid tripeptide) coupled alginate microencapsulation system in vitro and in vivo. Five-millimeter-diameter critical-size calvarial defects were created in immunocompromised mice and PDLSCs and GMSCs encapsulated in RGD-modified alginate microspheres were transplanted into the defect sites. New bone formation was assessed using microcomputed tomography and histological analyses 8 weeks after transplantation. Results confirmed that our microencapsulation system significantly enhanced MSC viability and osteogenic differentiation in vitro compared with non-RGD-containing alginate hydrogel microspheres with larger diameters. Results confirmed that PDLSCs were able to repair the calvarial defects by promoting the formation of mineralized tissue, while GMSCs showed significantly lower osteogenic differentiation capability. Further, results revealed that RGD-coupled alginate scaffold facilitated the differentiation of oral MSCs toward an osteoblast lineage in vitro and in vivo, as assessed by expression of osteogenic markers Runx2, ALP, and osteocalcin. In conclusion, these results for the first time demonstrated that MSCs derived from orofacial tissue encapsulated in RGD-modified alginate scaffold show promise for craniofacial bone regeneration. This treatment modality has many potential dental and orthopedic applications.

摘要

间充质干细胞 (MSCs) 为骨再生提供了一种优于当前治疗方式的有利治疗选择。然而,将 MSCs 递送到缺陷部位并保持高 MSC 存活率仍然是 MSC 介导的骨再生中的一个关键挑战。在这里,我们测试了包被在新型 RGD(精氨酸-甘氨酸-天冬氨酸三肽)偶联藻酸盐微囊化系统中的牙周膜干细胞 (PDLSCs) 和牙龈间充质干细胞 (GMSCs) 的体外和体内骨再生能力。在免疫缺陷小鼠中创建了 5 毫米直径的临界尺寸颅骨缺损,并将包被在 RGD 修饰的藻酸盐微球中的 PDLSCs 和 GMSCs 移植到缺陷部位。在移植后 8 周,使用 microCT 和组织学分析评估新骨形成。结果证实,与具有更大直径的不含 RGD 的藻酸盐水凝胶微球相比,我们的微囊化系统显著提高了 MSC 在体外的活力和成骨分化能力。结果证实 PDLSCs 能够通过促进矿化组织的形成来修复颅骨缺损,而 GMSCs 显示出明显较低的成骨分化能力。此外,结果表明,RGD 偶联的藻酸盐支架促进了口腔 MSCs 向成骨细胞谱系的体外和体内分化,这通过成骨标志物 Runx2、ALP 和骨钙素的表达来评估。总之,这些结果首次表明,包被在 RGD 修饰的藻酸盐支架中的源自口腔组织的 MSCs 具有颅面骨再生的潜力。这种治疗方式在牙科和骨科方面有许多潜在的应用。