i3S - Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Rua Alfredo Allen, 208, 4200 - 135 Porto, Portugal; INEB - Instituto de Engenharia Biomédica, Universidade do Porto, Rua Alfredo Allen, 208, 4200 - 135 Porto, Portugal; Faculdade de Engenharia, Universidade do Porto, Rua Dr. Roberto Frias, s/n, 4200-465 Porto, Portugal.
i3S - Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Rua Alfredo Allen, 208, 4200 - 135 Porto, Portugal; INEB - Instituto de Engenharia Biomédica, Universidade do Porto, Rua Alfredo Allen, 208, 4200 - 135 Porto, Portugal; ICBAS - Instituto de Ciências Biomédicas de Abel Salazar, Universidade do Porto, Rua de Jorge Viterbo Ferreira n. 228, 4050-313 Porto, Portugal.
Mater Sci Eng C Mater Biol Appl. 2019 Jun;99:1289-1303. doi: 10.1016/j.msec.2019.02.053. Epub 2019 Feb 16.
Strontium (Sr) is known to stimulate osteogenesis, while inhibiting osteoclastogenesis, thus encouraging research on its application as a therapeutic agent for bone repair/regeneration. It has been suggested that it may possess immunomodulatory properties, which might act synergistically in bone repair/regeneration processes. To further explore this hypothesis we have designed a Sr-hybrid system composed of an in situ forming Sr-crosslinked RGD-alginate hydrogel reinforced with Sr-doped hydroxyapatite (HAp) microspheres and studied its in vitro osteoinductive behaviour and in vivo inflammatory response. The Sr-hybrid scaffold acts as a dual Sr delivery system, showing a cumulative Sr release of ca. 0.3 mM after 15 days. In vitro studies using Srconcentrations within this range (0 to 3 mM Sr) confirmed its ability to induce osteogenic differentiation of mesenchymal stem/stromal cells (MSC), as well as to reduce osteoclastogenesis and osteoclasts (OC) functionality. In comparison with a similar Sr-free system, the Sr-hybrid system stimulated osteogenic differentiation of MSC, while inhibiting the formation of OC. Implantation in an in vivo model of inflammation, revealed an increase in F4/80/CD206 cells, highlighting its ability to modulate the inflammatory response as a pro-resolution mediator, through M2 macrophage polarization. Therefore, the Sr-hybrid system is potentially an appealing biomaterial for future clinical applications.
锶(Sr)被认为可以刺激成骨作用,同时抑制破骨细胞生成,因此促进了其作为骨修复/再生治疗剂的应用研究。有人提出,它可能具有免疫调节特性,这可能在骨修复/再生过程中协同作用。为了进一步探索这一假说,我们设计了一种由原位形成的 Sr 交联 RGD-藻酸盐水凝胶组成的 Sr 杂化系统,该水凝胶中掺入了 Sr 掺杂的羟基磷灰石(HAp)微球,并研究了其体外成骨行为和体内炎症反应。Sr 杂化支架作为一种双重 Sr 输送系统,在 15 天后可释放约 0.3 mM 的累积 Sr。在 Sr 浓度范围内(0 至 3 mM Sr)进行的体外研究证实了其诱导间充质干细胞(MSC)成骨分化的能力,以及减少破骨细胞生成和破骨细胞(OC)功能的能力。与类似的无 Sr 系统相比,Sr 杂化系统刺激 MSC 的成骨分化,同时抑制 OC 的形成。在炎症的体内模型植入中,F4/80/CD206 细胞增加,这突出了其作为促解决介质通过 M2 巨噬细胞极化来调节炎症反应的能力。因此,Sr 杂化系统可能是一种有吸引力的生物材料,适用于未来的临床应用。