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DOI 10.3109/08977194.2013.830611

Медицинская библиотека · Growth factors (Chur, Switzerland) · 2013

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

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

СтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

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.

Для цитирования: 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. GDFs promote tenogenic characteristics on human periodontal ligament-derived cells in culture at late passages.. Growth factors (Chur, Switzerland). 2013. DOI: 10.3109/08977194.2013.830611.

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