Qiu Huiqing, Zhang Liyan, He Xinqi, Wei Yusen, Wang Miaoran, Ma Bin, Hu Dailun, Shi Zhongli
Department of Geriatrics, The First Hospital of Hebei Medical University, Shijiazhuang, People's Republic of China.
Hebei Key Laboratory of Brain Science and Psychiatric-Psychologic Disease, Shijiazhuang, People's Republic of China.
J Food Biochem. 2022 Oct;46(10):e14329. doi: 10.1111/jfbc.14329. Epub 2022 Jul 22.
During the implantation of functional tissue-engineered constructs for treating bone defects, a functional vascular network is critical for the survival of the construct. One strategy to achieve rapid angiogenesis for this application is the co-culture of outgrowth endothelial cells (OECs) and primary human osteoblasts (POBs) within a scaffold prior to implantation. In the present study, we aim to investigate whether Astragalus polysaccharide (APS) promotes angiogenesis or vascularization via the TLR4 signaling pathway in a co-culture of OECs and POBs. The co-cultures were treated with various concentrations of APS for 24 h and, subsequently, another 7 days, followed by CD31 staining and analysis of micro-vessel-formation areas using software. Additionally, APS (0.4 mg/ml for 24 h) was added to monocultures of OECs or POBs for evaluating proliferation, apoptosis, angiogenesis, osteogenesis, TLR4 signaling pathway, and inflammatory cytokine release. We found that APS promoted angiogenesis in the co-culture at the optimal concentration of 0.4 mg/ml. TLR4 activation by APS up-regulated the expression level of TLR4/MyD88 and enhanced angiogenesis and osteogenesis in monocultures of OECs and POBs. The levels of E-selectin adhesion molecules, three cytokines (IL-6, TNF-α, and IFN-γ), and VEGF and PDGF-BB, which can induce angiogenesis, increased significantly (p < .05) following APS treatment. Therefore, APS appears to promote angiogenesis and ossification in the co-culture system via the TLR4 signaling pathway. PRACTICAL APPLICATIONS: This study demonstrates that APS may promote angiogenesis and osteocyte proliferation in OEC and POB co-culture systems through the MyD88-dependent TLR4 signaling pathway. APS might represent a potential therapeutic strategy in tissue-engineered bone implantation for the treatment of large bone defects; additionally, it has the advantage of safety, as it exhibits low or no side effects. In the future, it is expected to be used in vitro for the construction of tissue-engineered bone and in vivo after implantation in patients with bone defects for promoting rapid vascularization and ossification of tissue-engineered bone and early fusion with the recipient's bone. In addition, as a food additive, Astragalus membranaceus can be used as a tonic material in patients recovering from a fracture for promoting blood-vessel formation at the fracture site and fracture recovery. Combining traditional Chinese medicine with tissue engineering can provide further strategies for promoting the development of regenerative medicine.
在植入用于治疗骨缺损的功能性组织工程构建体过程中,功能性血管网络对于构建体的存活至关重要。实现该应用中快速血管生成的一种策略是在植入前将迁出内皮细胞(OECs)与原代人成骨细胞(POBs)在支架内共培养。在本研究中,我们旨在研究黄芪多糖(APS)是否通过TLR4信号通路在OECs和POBs共培养体系中促进血管生成或血管化。共培养物用不同浓度的APS处理24小时,随后再处理7天,然后进行CD31染色,并使用软件分析微血管形成区域。此外,将APS(0.4mg/ml,处理24小时)添加到OECs或POBs的单培养物中,以评估细胞增殖、凋亡、血管生成、成骨、TLR4信号通路和炎性细胞因子释放。我们发现,APS在0.4mg/ml的最佳浓度下促进了共培养体系中的血管生成。APS激活TLR4上调了TLR4/MyD88的表达水平,并增强了OECs和POBs单培养物中的血管生成和成骨。在APS处理后,E-选择素黏附分子、三种细胞因子(IL-6、TNF-α和IFN-γ)以及可诱导血管生成的VEGF和PDGF-BB的水平显著升高(p<0.05)。因此,APS似乎通过TLR4信号通路在共培养体系中促进血管生成和骨化。实际应用:本研究表明,APS可能通过MyD88依赖的TLR4信号通路促进OECs和POBs共培养体系中的血管生成和骨细胞增殖。APS可能代表了组织工程骨植入治疗大骨缺损的一种潜在治疗策略;此外,它具有安全性优势,因为其副作用低或无副作用。未来,有望将其用于体外构建组织工程骨,并在骨缺损患者体内植入后促进组织工程骨的快速血管化和骨化以及与受体骨的早期融合。此外,作为一种食品添加剂,黄芪可作为骨折恢复患者的滋补材料,用于促进骨折部位的血管形成和骨折恢复。将传统中药与组织工程相结合可为促进再生医学发展提供进一步的策略。
Exp Biol Med (Maywood). 2023-4
J Tissue Eng Regen Med. 2017-8-30
Exp Biol Med (Maywood). 2023-4