Ingénierie Moléculaire et Physiopathologie Articulaire (IMoPA), UMR 7365, CNRS-Université de Lorraine, Vandœuvre-Lès-Nancy, F-54505, France.
Department of Orthopedics, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
J Biomed Mater Res A. 2019 Jul;107(7):1406-1413. doi: 10.1002/jbm.a.36655. Epub 2019 Feb 25.
Angiogenesis is a critical parameter to consider for the development of tissue-engineered bone substitutes. The challenge is to promote sufficient vascularization in the bone substitute to prevent cell death and to allow its efficient integration. The capacity of nacre extract to restore the osteogenic activity of osteoarthritis osteoblasts has already been demonstrated. However, their angiogenic potential on endothelial progenitor cells (EPCs) was not yet explored. Therefore, the current study aimed at investigating if nacreous molecules affect EPC behavior. The gene and protein expression levels of endothelial cell (EC)-specific markers were determined in EPCs cultivated in presence of a nacre extract (ethanol soluble matrix [ESM] at two concentrations: 100 μg/mL and 200 μg/mL (respectively abbreviated ESM100 and ESM200)). Cell functionality was explored by proangiogenic factors production and in vitro tube formation assay. ESM200 increased the expression of some EC-specific genes. The in vitro tube formation assay demonstrated that ESM200 stimulated tubulogenesis affecting angiogenic parameters. We demonstrated that a stimulation with 200 μg/mL of ESM increased angiogenesis key elements. This in vitro study strongly highlights the proangiogenic effect of ESM. Due to its osteogenic properties, previously demonstrated, ESM could constitute the key element to develop an ideal prevascularized bone substitute. © 2019 Wiley Periodicals, Inc. J Biomed Mater Res Part A, 2019.
血管生成是组织工程骨替代物发展中需要考虑的关键参数。挑战在于促进骨替代物中的足够血管生成,以防止细胞死亡并允许其有效整合。珍珠层提取物恢复骨关节炎成骨细胞成骨活性的能力已经得到证实。然而,它们对内皮祖细胞(EPC)的血管生成潜力尚未得到探索。因此,本研究旨在研究珍珠层分子是否影响 EPC 行为。在存在珍珠层提取物(乙醇可溶基质[ESM]在两个浓度:100μg/mL 和 200μg/mL(分别缩写为 ESM100 和 ESM200))的情况下培养 EPC,确定内皮细胞(EC)特异性标志物的基因和蛋白表达水平。通过产生促血管生成因子和体外管形成试验来探索细胞功能。ESM200 增加了一些 EC 特异性基因的表达。体外管形成试验表明,ESM200 刺激了管形成,影响了血管生成参数。我们证明,用 200μg/mL 的 ESM 刺激增加了血管生成关键要素。这项体外研究强烈突出了 ESM 的促血管生成作用。由于其先前证明的成骨特性,ESM 可能成为开发理想的预血管化骨替代物的关键要素。©2019 年 Wiley 期刊,Inc. J 生物医学材料研究 A 部分,2019 年。