Jagiellonian University, Faculty of Biology, Institute of Zoology and Biomedical Research, Dept. Biology and Cell Imaging, Gronostajowa 9, 30-387 Krakow, Poland.
AGH University of Science and Technology, Faculty of Materials Science and Ceramics, Department of Glass Technology and Amorphous Coatings, 30 Mickiewicza Ave., 30-059 Krakow, Poland.
Mater Sci Eng C Mater Biol Appl. 2020 Apr;109:110535. doi: 10.1016/j.msec.2019.110535. Epub 2019 Dec 9.
We obtained a range of PLGA-based composites containing sol-gel bioactive glasses (SBG) from the SiO-CaO and SiO-CaO-PO systems. Eight SBGs with different CaO/SiO ratios with and without PO were incorporated at 50% w/w to PLGA matrix and structured into thin films suitable for cell culture. The SBG/PLGA composites were examined for their bioactivity in simulated body fluid (SBF), ion release profile in culture media with and without cells, and osteoinductivity in standard human bone marrow stromal cell (hBMSC) cultures without osteogenic growth factors. Our results indicate different surface activity of composites depending on the presence/absence of PO in SBG composition. Furthermore, ion release profile to culture medium differed depending on the presence/absence of cells. Direct culture of hBMSC on the SiO-CaO/PLGA composite films resulted in elevated Runx-2 mRNA, opposite to low Runx-2 mRNA levels on SiO-CaO-PO/PLGA films. All studied composites increased Osx mRNA levels. Whereas some of SiO-CaO/PLGA composites did not elevate BMP-2 and -6 proteins in hBMSC cultures, high levels of these BMPs were present in all cultures on SiO-CaO-PO/PLGA composites. All composites induced BMP-related Tak1 signalling, whereas Smad1 signalling was restricted mostly to composites containing three-component SBGs. ALP activity of hBMSC and BMP-related luciferase activity of mouse BRITE cells differed depending on whether the cells were stimulated with culture medium conditioned with SBG/PLGA composites or the cells were directly cultured on the composite surfaces. Altogether, beyond bioactivity and osteoinductivity of SBG/PLGA composites, our studies show key differences in the biological response to both the bioactive material dissolution products and upon direct cell-material contacts.
我们从 SiO-CaO 和 SiO-CaO-PO 系统中获得了一系列含有溶胶-凝胶生物活性玻璃 (SBG) 的 PLGA 基复合材料。将 8 种不同 CaO/SiO 比的 SBG 与或不与 PO 一起以 50% w/w 的比例掺入 PLGA 基质中,并将其构建成适合细胞培养的薄膜。在模拟体液 (SBF) 中对 SBG/PLGA 复合材料的生物活性进行了研究,在有细胞和无细胞的培养基中研究了离子释放情况,并在没有成骨生长因子的标准人骨髓基质细胞 (hBMSC) 培养物中研究了成骨诱导能力。我们的结果表明,复合材料的表面活性取决于 SBG 成分中 PO 的存在/不存在。此外,离子释放情况因细胞的存在/不存在而有所不同。将 hBMSC 直接培养在 SiO-CaO/PLGA 复合膜上会导致 Runx-2 mRNA 升高,而 SiO-CaO-PO/PLGA 膜上的 Runx-2 mRNA 水平较低。所有研究的复合材料均增加了 Osx mRNA 水平。虽然一些 SiO-CaO/PLGA 复合材料没有在 hBMSC 培养物中升高 BMP-2 和 -6 蛋白的水平,但在 SiO-CaO-PO/PLGA 复合材料的所有培养物中均存在这些 BMPs 的高水平。所有复合材料均诱导了与 BMP 相关的 Tak1 信号转导,而 Smad1 信号转导主要局限于含有三组分 SBG 的复合材料。hBMSC 的碱性磷酸酶 (ALP)活性和小鼠 BRITE 细胞的 BMP 相关荧光素酶活性取决于细胞是用 SBG/PLGA 复合材料条件培养基刺激还是直接在复合材料表面培养。总的来说,除了 SBG/PLGA 复合材料的生物活性和成骨诱导性之外,我们的研究还显示了对生物活性材料溶解产物和直接细胞-材料接触的生物学反应之间的关键差异。