State Key Laboratory of Military Stomatology Department of Periodontology, School of Stomatology, Fourth Military Medical University, Xi'an, P.R. China; National Clinical Research Center for Oral Diseases, Department of Periodontology, School of Stomatology, Fourth Military Medical University, Xi'an, P.R. China; Shaanxi Engineering Research Center for Dental Materials and Advanced Manufacture, Department of Periodontology, School of Stomatology, Fourth Military Medical University, Xi'an, P.R. China.
State Key Laboratory of Military Stomatology Department of Periodontology, School of Stomatology, Fourth Military Medical University, Xi'an, P.R. China.
Acta Biomater. 2019 Apr 1;88:162-180. doi: 10.1016/j.actbio.2019.02.004. Epub 2019 Feb 5.
Recently, we found that although high-stiffness matrices stimulated osteogenic differentiation of bone marrow-derived stromal cells (BMSCs), the macrophages (Mφs) in high-stiffness transglutaminase crosslinked gelatins (TG-gels) tended to undergo M1 polarization and hence compromised cell osteogenesis. In this study, we hypothesized that the copresentation of interleukin (IL)-4 and stromal cell-derived factor (SDF)-1α in high-stiffness TG-gels may enhance periodontal regeneration by modulating Mφ polarization and promoting endogenous stem cell recruitment. We found that Mφs were more likely to polarize toward an immunomodulatory M2 state in the presence of IL-4 and hence positively influence the osteogenic differentiation of BMSCs when these cells coexisted in either indirect or direct co-culture systems. In cell migration assays, BMSCs exhibited an enhanced capability to move toward gels containing SDF-1α, and more cells could be recruited into the three-dimensional matrix of TG-gels. When TG-gels containing IL-4 and/or SDF-1α were used to repair periodontal defects, more new bone (MicroCT) was formed in animals that received the dual cytokine-loaded transplants at 4 weeks postsurgery. Mφs were recruited to all the transplanted gels, and after one week, more M1-phenotype cells were found in the groups without IL-4, while the presence of IL-4 was more likely to result in M2 polarization (immunofluorescence staining). When the tissue biopsies were histologically examined, the TG-gels containing both IL-4 and SDF-1α led to a generally satisfactory regeneration with respect to attachment recovery (epithelial and connective tissue) and hybrid tissue regeneration (bone, periodontal ligament and cementum). Our data suggest that the incorporation of IL-4 into high-stiffness TG-gels may promote the M2 polarization of Mφs and that SDF-1α can be applied to guide endogenous cell homing. Overall, building capacity for Mφ modulation and cell recruitment in high-stiffness hydrogels represents a simple and effective strategy that can support high levels of periodontal tissue regeneration. STATEMENT OF SIGNIFICANCE: The development of hydrogel-based regenerative therapies centered on the mobilization and stimulation of native cells for therapeutics opens a window toward realizing periodontal endogenous regeneration. In the present study, the parallel use of immunomodulatory and homing factors in high-stiffness hydrogel materials is shown to induce stem cell homing, modulate cell differentiation and indeed induce regrowth of the periodontium. We found that incorporation of interleukin (IL)-4 in high-stiffness TG-gels coaxed macrophages to polarize into M2 phenotypes, and stromal cell-derived factor (SDF)-1α could be applied to direct endogenous cell homing. Hence, we present for the first time a clinically relevant strategy based on macrophage modulation and host cell recruitment that can support high levels of periodontal tissue regeneration.
最近,我们发现,尽管高刚性基质能刺激骨髓基质细胞(BMSCs)的成骨分化,但高刚性转谷氨酰胺酶交联明胶(TG-凝胶)中的巨噬细胞(Mφ)倾向于发生 M1 极化,从而损害细胞成骨。在这项研究中,我们假设白细胞介素(IL)-4 和基质细胞衍生因子(SDF)-1α在高刚性 TG-凝胶中的共表达可能通过调节 Mφ 极化和促进内源性干细胞募集来增强牙周再生。我们发现,当 IL-4 和 BMSCs 同时存在于间接或直接共培养系统中时,Mφ 更有可能向免疫调节 M2 状态极化,从而积极影响 BMSCs 的成骨分化。在细胞迁移实验中,BMSCs 表现出向含有 SDF-1α 的凝胶迁移的增强能力,并且更多的细胞可以募集到 TG-凝胶的三维基质中。当含有 IL-4 和/或 SDF-1α 的 TG-凝胶用于修复牙周缺损时,在手术后 4 周接受双细胞因子负载移植的动物中,形成了更多的新骨(MicroCT)。Mφ 被募集到所有移植的凝胶中,一周后,在没有 IL-4 的组中发现更多的 M1 表型细胞,而 IL-4 的存在更有可能导致 M2 极化(免疫荧光染色)。当组织活检进行组织学检查时,含有 IL-4 和 SDF-1α 的 TG-凝胶导致附着恢复(上皮和结缔组织)和混合组织再生(骨、牙周韧带和牙骨质)方面的总体令人满意的再生。我们的数据表明,将 IL-4 纳入高刚性 TG-凝胶中可能会促进 Mφ 的 M2 极化,并且 SDF-1α 可用于指导内源性细胞归巢。总之,在高刚性水凝胶中构建 Mφ 调节和细胞募集的能力代表了一种简单有效的策略,可以支持高水平的牙周组织再生。
以动员和刺激天然细胞进行治疗为中心的基于水凝胶的再生疗法的发展为实现牙周内源性再生开辟了一扇窗。在本研究中,在高刚性水凝胶材料中平行使用免疫调节和归巢因子被证明可以诱导干细胞归巢、调节细胞分化,并确实诱导牙周组织的再生。我们发现,将白细胞介素(IL)-4 纳入高刚性 TG-凝胶中可以诱导巨噬细胞向 M2 表型极化,基质细胞衍生因子(SDF)-1α 可用于指导内源性细胞归巢。因此,我们首次提出了一种基于巨噬细胞调节和宿主细胞募集的临床相关策略,该策略可以支持高水平的牙周组织再生。