Department of Biologic and Materials Science, Division of Prosthodontics, University of Michigan School of Dentistry, Ann Arbor, MI 48109, USA.
Macromolecular Science and Engineering Center, College of Engineering, University of Michigan, Ann Arbor, MI 48109, USA.
Int J Mol Sci. 2022 Apr 19;23(9):4499. doi: 10.3390/ijms23094499.
Tissue engineering aims to repair, restore, and/or replace tissues in the human body as an alternative to grafts and prostheses. Biomaterial scaffolds can be utilized to provide a three-dimensional microenvironment to facilitate tissue regeneration. Previously, we reported that scaffold pore size influences vascularization and extracellular matrix composition both in vivo and in vitro, to ultimately influence tissue phenotype for regenerating cranial suture and bone tissues, which have markedly different tissue properties despite similar multipotent stem cell populations. To rationally design biomaterials for specific cell and tissue fate specification, it is critical to understand the molecular processes governed by cell-biomaterial interactions, which guide cell fate specification. Building on our previous work, in this report we investigated the hypothesis that scaffold pore curvature, the direct consequence of pore size, modulates the differentiation trajectory of mesenchymal stem cells (MSCs) through alterations in the cytoskeleton. First, we demonstrated that sufficiently small pores facilitate cell clustering in subcutaneous explants cultured in vivo, which we previously reported to demonstrate stem tissue phenotype both in vivo and in vitro. Based on this observation, we cultured cell-scaffold constructs in vitro to assess early time point interactions between cells and the matrix as a function of pore size. We demonstrate that principle curvature directly influences nuclear aspect and cell aggregation in vitro. Scaffold pores with a sufficiently low degree of principle curvature enables cell differentiation; pharmacologic inhibition of actin cytoskeleton polymerization in these scaffolds decreased differentiation, indicating a critical role of the cytoskeleton in transducing cues from the scaffold pore microenvironment to the cell nucleus. We fabricated a macropore model, which allows for three-dimensional confocal imaging and demonstrates that a higher principle curvature facilitates cell aggregation and the formation of a potentially protective niche within scaffold macropores which prevents MSC differentiation and retains their stemness. Sufficiently high principle curvature upregulates yes-associated protein (YAP) phosphorylation while decreased principle curvature downregulates YAP phosphorylation and increases YAP nuclear translocation with subsequent transcriptional activation towards an osteogenic differentiation fate. Finally, we demonstrate that the inhibition of the YAP/TAZ pathway causes a defect in differentiation, while YAP/TAZ activation causes premature differentiation in a curvature-dependent way when modulated by verteporfin (VP) and 1-oleyl-lysophosphatidic acid (LPA), respectively, confirming the critical role of biomaterials-mediated YAP/TAZ signaling in cell differentiation and fate specification. Our data support that the principle curvature of scaffold macropores is a critical design criterion which guides the differentiation trajectory of mesenchymal stem cells' scaffolds. Biomaterial-mediated regulation of YAP/TAZ may significantly contribute to influencing the regenerative outcomes of biomaterials-based tissue engineering strategies through their specific pore design.
组织工程旨在修复、恢复和/或替代人体组织,作为移植物和假体的替代物。生物材料支架可用于提供三维微环境,以促进组织再生。以前,我们报道支架孔大小会影响体内和体外的血管生成和细胞外基质组成,最终影响颅缝和骨骼组织的组织表型,尽管它们具有相似的多能干细胞群体,但组织特性却明显不同。为了合理设计用于特定细胞和组织命运指定的生物材料,了解细胞-生物材料相互作用所控制的分子过程至关重要,这些过程指导细胞命运指定。在此基础上,我们在前人的工作基础上,提出假设认为支架孔曲率(孔大小的直接结果)通过改变细胞骨架来调节间充质干细胞(MSCs)的分化轨迹。首先,我们证明了足够小的孔有利于在体内培养的皮下外植体中的细胞聚集,我们之前报道过这种聚集体在体内和体外均表现出干细胞组织表型。基于这一观察结果,我们在体外培养细胞-支架构建体,以评估细胞与基质之间的早期时间点相互作用作为孔大小的函数。我们证明主曲率直接影响体外的核形态和细胞聚集。支架孔具有足够低的主曲率可以促进细胞分化;在这些支架中抑制肌动蛋白细胞骨架聚合会减少分化,表明细胞骨架在将支架孔微环境中的信号转导到细胞核中起着关键作用。我们制造了一个大孔模型,该模型允许进行三维共聚焦成像,并证明较高的主曲率有助于细胞聚集,并在支架大孔内形成潜在的保护性小生境,从而阻止 MSC 分化并保持其干性。足够高的主曲率会增加 YAP 磷酸化,而降低主曲率会降低 YAP 磷酸化并增加 YAP 核易位,从而随后朝着成骨分化命运进行转录激活。最后,我们证明 YAP/TAZ 通路的抑制会导致分化缺陷,而 YAP/TAZ 的激活会导致在曲率依赖性方式下过早分化,分别通过verteporfin(VP)和 1-油酰基-溶血磷脂酸(LPA)进行调节,这证实了生物材料介导的 YAP/TAZ 信号在细胞分化和命运指定中的关键作用。我们的数据支持支架大孔的主曲率是指导间充质干细胞支架分化轨迹的关键设计标准。生物材料介导的 YAP/TAZ 调节可能通过其特定的孔设计显著有助于影响基于生物材料的组织工程策略的再生结果。