Department of Oral Biology, School of Dental Medicine, University of Buffalo, The State University of New York, Buffalo, NY, USA; Department of Orthopedics, Fourth Affiliated Hospital, China Medical University, Shenyang, China.
Department of Oral Biology, School of Dental Medicine, University of Buffalo, The State University of New York, Buffalo, NY, USA.
Mol Ther. 2018 Jan 3;26(1):199-207. doi: 10.1016/j.ymthe.2017.09.011. Epub 2017 Sep 14.
Repair and regeneration of inflammation-induced bone loss remains a clinical challenge. LL37, an antimicrobial peptide, plays critical roles in cell migration, cytokine production, apoptosis, and angiogenesis. Migration of stem cells to the affected site and promotion of vascularization are essential for tissue engineering therapy, including bone regeneration. However, it is largely unknown whether LL37 affects mesenchymal stem cell (MSC) behavior and bone morphogenetic protein 2 (BMP2)-mediated bone repair during the bone pathologic remodeling process. By performing in vitro and in vivo studies with MSCs and a lipopolysaccharide (LPS)-induced mouse calvarial osteolytic bone defect model, we found that LL37 significantly promotes cell differentiation, migration, and proliferation in both unmodified MSCs and BMP2 gene-modified MSCs. Additionally, LL37 inhibited LPS-induced osteoclast formation and bacterial activity in vitro. Furthermore, the combination of LL37 and BMP2 markedly promoted MSC-mediated angiogenesis and bone repair and regeneration in LPS-induced osteolytic defects in mouse calvaria. These findings demonstrate for the first time that LL37 can be a potential candidate drug for promoting osteogenesis and for inhibiting bacterial growth and osteoclastogenesis, and that the combination of BMP2 and LL37 is ideal for MSC-mediated bone regeneration, especially for inflammation-induced bone loss.
炎症诱导的骨丢失的修复和再生仍然是一个临床挑战。LL37 是一种抗菌肽,在细胞迁移、细胞因子产生、细胞凋亡和血管生成中发挥关键作用。干细胞迁移到受影响的部位和促进血管生成对于组织工程治疗,包括骨再生,是必不可少的。然而,目前尚不清楚 LL37 是否会影响间充质干细胞(MSC)在骨病理重塑过程中的行为和骨形态发生蛋白 2(BMP2)介导的骨修复。通过对 MSC 进行体外和体内研究,并利用脂多糖(LPS)诱导的小鼠颅骨溶骨性骨缺损模型,我们发现 LL37 可显著促进未修饰的 MSC 和 BMP2 基因修饰的 MSC 的细胞分化、迁移和增殖。此外,LL37 在体外抑制 LPS 诱导的破骨细胞形成和细菌活性。此外,LL37 和 BMP2 的联合应用显著促进了 MSC 介导的血管生成和 LPS 诱导的小鼠颅骨溶骨性缺损中的骨修复和再生。这些发现首次表明,LL37 可以成为一种有潜力的候选药物,用于促进成骨作用,抑制细菌生长和破骨细胞生成,并且 BMP2 和 LL37 的联合应用是 MSC 介导的骨再生的理想选择,特别是对于炎症诱导的骨丢失。