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骨形态发生蛋白-9通过JNK信号通路增强人牙周膜干细胞的成骨分化

Bone Morphogenetic Protein-9 Enhances Osteogenic Differentiation of Human Periodontal Ligament Stem Cells via the JNK Pathway.

作者信息

Wang Pei, Wang Yanen, Tang Weizhong, Wang Xingxing, Pang Yanan, Yang Su, Wei Yibo, Gao Haochen, Wang Dalin, Cao Zhizhong

机构信息

Department of Stomatology, Changhai Hospital, Second Military Medical University, Shanghai, China.

Clinical research center, Changhai Hospital, Second Military Medical University, Shanghai, China.

出版信息

PLoS One. 2017 Jan 4;12(1):e0169123. doi: 10.1371/journal.pone.0169123. eCollection 2017.

Abstract

Bone morphogenetic protein-9 (BMP9) shows great osteoinductive potential in bone regeneration. Periodontal ligament stem cells (PDLSCs) with multi-differentiation capability and low immunogenicity are increasingly used as seed cells for periodontal regenerative therapies. In the present study, we investigated the potent osteogenic activity of BMP9 on human PDLSCs (hPDLSCs), in which the c-Jun N-terminal kinase (JNK) pathway is possibly involved. Our results showed that JNK inhibition by the specific inhibitor SP600125 or adenovirus expressing small interfering RNA (siRNA) targeting JNK (AdR-si-JNK) significantly decreased BMP9-induced gene and protein expression of early and late osteogenic markers, such as runt-related transcription factor 2 (Runx2), alkaline phosphatase (ALP), osteopontin (OPN), and osteocalcin (OCN), in hPDLSCs. We also confirmed the in-vivo positive effect of JNKs on ectopic bone formation induced by hPDLSCs injected into the musculature of athymic nude mice and BMP9 ex vivo gene delivery. For the cellular mechanism, we found that BMP9 activated the phosphorylation of JNKs and Smad2/3, and that JNKs may engage in cross-talk with the Smad2/3 pathway in BMP9-mediated osteogenesis.

摘要

骨形态发生蛋白-9(BMP9)在骨再生中显示出巨大的骨诱导潜力。具有多向分化能力和低免疫原性的牙周膜干细胞(PDLSCs)越来越多地被用作牙周再生治疗的种子细胞。在本研究中,我们研究了BMP9对人牙周膜干细胞(hPDLSCs)的强大成骨活性,其中c-Jun氨基末端激酶(JNK)通路可能参与其中。我们的结果表明,用特异性抑制剂SP600125或表达靶向JNK的小干扰RNA(siRNA)的腺病毒(AdR-si-JNK)抑制JNK可显著降低BMP9诱导的hPDLSCs中早期和晚期成骨标志物的基因和蛋白表达,如 runt相关转录因子2(Runx2)、碱性磷酸酶(ALP)、骨桥蛋白(OPN)和骨钙素(OCN)。我们还证实了JNK对注入无胸腺裸鼠肌肉组织的hPDLSCs和BMP9体外基因递送诱导的异位骨形成的体内积极作用。对于细胞机制,我们发现BMP9激活了JNK和Smad2/3的磷酸化,并且JNK可能在BMP9介导的成骨过程中与Smad2/3通路发生相互作用。

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