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生长分化因子(GDFs)在传代后期培养的人牙周膜来源细胞上促进肌腱生成特性。

GDFs promote tenogenic characteristics on human periodontal ligament-derived cells in culture at late passages.

作者信息

Xia Dengsheng, Sumita Yoshinori, Liu Younan, Tai Yunlin, Wang Jinsong, Uehara Masataka, Agata Hideki, Kagami Hideaki, Fan Zhipeng, Asahina Izumi, Wang Songlin, Tran Simon D

机构信息

Salivary Gland Disease Center and Molecular Laboratory for Gene Therapy & Tooth Regeneration, Capital Medical University School of Stomatology , Beijing , China .

出版信息

Growth Factors. 2013 Oct;31(5):165-73. doi: 10.3109/08977194.2013.830611.

Abstract

Tendon/ligament injures are leading disabilities worldwide. The periodontal ligament (PDL) connects teeth to bone, and is comparable to a tendon/ligament-to-bone insertion. PDL-derived cells (PDLCs) express both osteo/cementogenesis and teno/ligamentogenesis genes. However, an efficient method to induce a tenogenic differentiation of PDLCs has not been thoroughly examined. Therefore, this study tested if growth/differentiation factors (GDFs) enhanced tenogenic characteristics of human PDLCs, as a potential cell source for tendon/ligament engineering. Results demonstrated recombinant GDF-5/GDF-7 inhibited alkaline phosphatase (ALP) activity of PDLCs from passage 3 to 6, while GDF-5 enhanced ALP in dental pulp-derived cells and mesenchymal stem cells. GDF-5 (particularly at 10 ng/ml concentration) induced high expression of both early (scleraxis) and mature (tenomodulin, aggrecan, collagen3) tenogenic genes in P4-6 PDLCs, while inhibiting expression of specific transcription-factors for osteogenic, chondrogenic and adipogenic differentiation. Exogenous GDFs might lead PDLCs being expanded in culture during several passages to highly useful cell source for tendon/ligament engineering.

摘要

肌腱/韧带损伤是全球主要的致残原因。牙周韧带(PDL)将牙齿与骨骼相连,类似于肌腱/韧带与骨骼的附着结构。牙周韧带来源的细胞(PDLCs)同时表达成骨/牙骨质生成基因和肌腱/韧带生成基因。然而,一种有效诱导PDLCs向肌腱分化的方法尚未得到充分研究。因此,本研究测试了生长/分化因子(GDFs)是否能增强人PDLCs的肌腱生成特性,作为肌腱/韧带工程的潜在细胞来源。结果表明,重组GDF-5/GDF-7抑制了第3至6代PDLCs的碱性磷酸酶(ALP)活性,而GDF-5增强了牙髓来源细胞和间充质干细胞中的ALP活性。GDF-5(特别是在10 ng/ml浓度下)诱导第4至6代PDLCs中早期(硬骨素)和成熟(肌腱调节蛋白、聚集蛋白聚糖、胶原蛋白3)肌腱生成基因的高表达,同时抑制成骨、软骨生成和脂肪生成分化的特异性转录因子的表达。外源性GDFs可能使PDLCs在培养传代过程中扩增,成为肌腱/韧带工程中非常有用的细胞来源。

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