Han Pingping, Xu Mengchi, Chang Jiang, Chakravorty Nishant, Wu Chengtie, Xiao Yin
Institute of Health & Biomedical Innovation, Queensland University of Technology, Brisbane, Queensland 4059, Australia.
Biomater Sci. 2014 Sep 29;2(9):1230-1243. doi: 10.1039/c4bm00111g. Epub 2014 Jun 5.
It is accepted that the accelerated differentiation of tissue cells on bioactive materials is of great importance to regenerate the lost tissues. It was previously reported that lithium (Li) ions could enhance the in vitro proliferation and differentiation of retinoblastoma cells and endometrium epithelia by activating the Wnt canonical signalling pathway. It is interesting to incorporate Li ions into bioactive ceramics, such as β-tricalcium phosphate (Li-β-TCP), in order to stimulate both osteogenic and cementogenic differentiation of different stem cells for the regeneration of bone/periodontal tissues. Therefore, the aim of this study was to investigate the interactions of human periodontal ligament cells (hPDLCs) and human bone marrow stromal cells (hBMSCs) with Li-β-TCP bioceramic bulks and their ionic extracts, and further explore the osteogenic and cementogenic stimulation of Li-β-TCP bioceramics and the possible molecular mechanisms. The results showed that Li-β-TCP bioceramic disks supported the cell attachment and proliferation, and significantly enhanced bone/cementum-related gene expression, Wnt canonical signalling pathway activation for both hPDLCs and hBMSCs, compared to conventional β-TCP bioceramic disks without Li. The release of Li from Li-β-TCP powders could significantly promote the bone/cementum-related gene expression for both hPDLCs and hBMSCs compared to pure β-TCP extracts without Li release. Our results suggest that the combination of Li with β-TCP bioceramics may be a promising method to enhance bone/cementum regeneration as Li-β-TCP possesses excellent in vitro osteogenic and cementogenic stimulation properties by inducing bone/cementum-related gene expression in both hPDLCs and hBMSCs.
人们普遍认为,生物活性材料上组织细胞的加速分化对于再生受损组织至关重要。此前有报道称,锂离子可通过激活Wnt经典信号通路来增强视网膜母细胞瘤细胞和子宫内膜上皮细胞的体外增殖与分化。将锂离子掺入生物活性陶瓷(如β - 磷酸三钙,Li-β-TCP)中,以刺激不同干细胞的成骨和成牙骨质分化,从而实现骨/牙周组织的再生,这一点很有意思。因此,本研究的目的是探究人牙周膜细胞(hPDLCs)和人骨髓间充质干细胞(hBMSCs)与Li-β-TCP生物陶瓷块及其离子提取物之间的相互作用,并进一步探索Li-β-TCP生物陶瓷的成骨和成牙骨质刺激作用以及可能的分子机制。结果表明,与不含锂的传统β-TCP生物陶瓷盘相比,Li-β-TCP生物陶瓷盘支持细胞附着和增殖,并显著增强了hPDLCs和hBMSCs与骨/牙骨质相关的基因表达以及Wnt经典信号通路的激活。与不释放锂的纯β-TCP提取物相比,Li-β-TCP粉末中锂的释放可显著促进hPDLCs和hBMSCs与骨/牙骨质相关的基因表达。我们的结果表明,锂与β-TCP生物陶瓷的结合可能是一种有前景的增强骨/牙骨质再生的方法,因为Li-β-TCP通过诱导hPDLCs和hBMSCs中与骨/牙骨质相关的基因表达,具有出色的体外成骨和成牙骨质刺激特性。