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本文引用的文献

1
The healing effects of autologous platelet gel on acute human skin wounds.自体血小板凝胶对人类急性皮肤伤口的愈合作用。
Arch Facial Plast Surg. 2007 May-Jun;9(3):174-83. doi: 10.1001/archfaci.9.3.174.
2
Cellular effects of platelet rich plasma: a study on HL-60 macrophage-like cells.富血小板血浆的细胞效应:对HL-60巨噬细胞样细胞的研究
Biomed Sci Instrum. 2007;43:266-71.
3
Platelet-rich plasma: growth factors and pro- and anti-inflammatory properties.富血小板血浆:生长因子以及促炎和抗炎特性。
J Periodontol. 2007 Apr;78(4):661-9. doi: 10.1902/jop.2007.060302.
4
Variation of pH in lysed platelet concentrates influence proliferation and alkaline phosphatase activity in human osteoblast-like cells.裂解血小板浓缩物中pH值的变化会影响人成骨样细胞的增殖和碱性磷酸酶活性。
Platelets. 2007 Mar;18(2):113-8. doi: 10.1080/09537100600800537.
5
Antibacterial effect of autologous platelet gel enriched with growth factors and other active substances: an in vitro study.富含生长因子及其他活性物质的自体血小板凝胶的抗菌作用:一项体外研究
J Bone Joint Surg Br. 2007 Mar;89(3):417-20. doi: 10.1302/0301-620X.89B3.18491.
6
Reciprocal actions of platelet-secreted TGF-beta1 on the production of VEGF and HGF by human tendon cells.血小板分泌的转化生长因子-β1对人肌腱细胞产生血管内皮生长因子和肝细胞生长因子的相互作用。
Plast Reconstr Surg. 2007 Mar;119(3):950-9. doi: 10.1097/01.prs.0000255543.43695.1d.
7
Human AB serum and thrombin-activated platelet-rich plasma are suitable alternatives to fetal calf serum for the expansion of mesenchymal stem cells from adipose tissue.人AB血清和凝血酶激活的富血小板血浆是用于从脂肪组织中扩增间充质干细胞的胎牛血清的合适替代品。
Stem Cells. 2007 May;25(5):1270-8. doi: 10.1634/stemcells.2006-0627. Epub 2007 Jan 25.
8
Platelet-rich plasma inhibits demineralized bone matrix-induced bone formation in nude mice.富含血小板的血浆抑制去矿化骨基质诱导的裸鼠骨形成。
J Bone Joint Surg Am. 2007 Jan;89(1):139-47. doi: 10.2106/JBJS.F.00388.
9
Platelet rich plasma (PRP) enhances anabolic gene expression patterns in flexor digitorum superficialis tendons.富含血小板血浆(PRP)可增强指浅屈肌腱中的合成代谢基因表达模式。
J Orthop Res. 2007 Feb;25(2):230-40. doi: 10.1002/jor.20278.
10
Comparison of surgically repaired Achilles tendon tears using platelet-rich fibrin matrices.使用富血小板纤维蛋白基质对手术修复的跟腱撕裂进行比较。
Am J Sports Med. 2007 Feb;35(2):245-51. doi: 10.1177/0363546506294078. Epub 2006 Nov 12.

缓冲富血小板血浆可增强间充质干细胞的增殖和软骨形成分化。

Buffered platelet-rich plasma enhances mesenchymal stem cell proliferation and chondrogenic differentiation.

作者信息

Mishra Allan, Tummala Padmaja, King Aaron, Lee Byung, Kraus Mark, Tse Victor, Jacobs Christopher R

机构信息

Menlo Sports Medicine, Menlo Park, California., USA.

出版信息

Tissue Eng Part C Methods. 2009 Sep;15(3):431-5. doi: 10.1089/ten.tec.2008.0534.

DOI:10.1089/ten.tec.2008.0534
PMID:19216642
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2819709/
Abstract

The success of tissue engineering applications can potentially be dramatically improved with the addition of adjuncts that increase the proliferation and differentiation of progenitor or stem cells. Platelet-rich plasma (PRP) has recently emerged as a potential biologic tool to treat acute and chronic tendon disorders. The regenerative potential of PRP is based on the release of growth factors that occurs with platelet rupture. Its autologous nature gives it a significant advantage in tissue engineering applications. To test whether PRP may be useful specifically for cartilage regeneration, a cell culture experiment was devised in which mesenchymal stem cells (MSCs) were grown in control media or media enhanced with inactivated, buffered PRP. Proliferation 7 days after PRP treatment was increased: 1.041 versus 0.199 for the control media cells ( p<0.001). The messenger RNA (mRNA) level of the osteogenic marker RUNX2 was 52.84 versus 26.88 for the control group ( p<0.005). Likewise the mRNA level of the chondrogenic markers Sox-9 and aggrecan was 29.74 versus 2.29 for the control group ( p<0.001) and 21.04 versus 1.93 ( p<0.001), respectively. These results confirm that PRP enhances MSC proliferation and suggest that PRP causes chondrogenic differentiation of MSC in vitro.

摘要

通过添加能够促进祖细胞或干细胞增殖与分化的辅助剂,组织工程应用的成功率可能会得到显著提高。富血小板血浆(PRP)最近已成为治疗急慢性肌腱疾病的一种潜在生物工具。PRP的再生潜力基于血小板破裂时生长因子的释放。其自体性质使其在组织工程应用中具有显著优势。为了测试PRP是否特别有助于软骨再生,设计了一项细胞培养实验,其中间充质干细胞(MSCs)在对照培养基或添加了灭活缓冲PRP的培养基中培养。PRP处理7天后细胞增殖增加:对照培养基中的细胞为0.199,而PRP处理组为1.041(p<0.001)。成骨标志物RUNX2的信使核糖核酸(mRNA)水平在对照组为26.88,而在PRP处理组为52.84(p<0.005)。同样,软骨生成标志物Sox-9和聚集蛋白聚糖的mRNA水平在对照组分别为2.29和1.93,而在PRP处理组分别为29.74和(p<均0.001)。这些结果证实PRP可增强MSCs的增殖,并表明PRP可在体外诱导MSCs向软骨细胞分化。