Department of Biomedical Engineering, New Jersey Institute of Technology, Newark, NJ, USA.
Department of Oral Biology, Department of Endodontics, Rutgers School of Dental Medicine, Newark, NJ, USA.
Acta Biomater. 2021 May;126:109-118. doi: 10.1016/j.actbio.2021.03.001. Epub 2021 Mar 6.
Angiogenesis is critical for tissue healing and regeneration. Promoting angiogenesis in materials implanted within dental pulp after pulpectomy is a major clinical challenge in endodontics. We demonstrate the ability of acellular self-assembling peptide hydrogels to create extracellular matrix mimetic architectures that guide in vivo development of neovasculature and tissue deposition. The hydrogels possess facile injectability, as well as sequence-level functionalizability. We explore the therapeutic utility of an angiogenic hydrogel to regenerate vascularized pulp-like soft tissue in a large animal (canine) orthotopic model. The regenerated soft tissue recapitulates key features of native pulp, such as blood vessels, neural filaments, and an odontoblast-like layer next to dentinal tubules. Our study establishes angiogenic peptide hydrogels as potent scaffolds for promoting soft tissue regeneration in vivo. STATEMENT OF SIGNIFICANCE: A major challenge to endodontic tissue engineering is the lack of in situ angiogenesis within intracanal implants, especially after complete removal of the dental pulp. The lack of a robust vasculature in implants limit integration of matrices with the host tissue and regeneration of soft tissue. We demonstrate the development of an acellular material that promotes tissue revascularization in vivo without added growth factors, in a preclinical canine model of pulp-like soft-tissue regeneration. Such acellular biomaterials would facilitate pulp revascularization approaches in large animal models, and translation into human clinical trials.
血管生成对于组织愈合和再生至关重要。在牙髓切除术后,在牙髓内植入的材料中促进血管生成是牙髓病学中的一个主要临床挑战。我们展示了无细胞自组装肽水凝胶的能力,这种水凝胶可以创建模仿细胞外基质的结构,从而引导体内新生血管和组织沉积的发育。这些水凝胶具有易于注射的特性,以及序列水平的功能化能力。我们探索了一种血管生成水凝胶的治疗效用,以在大型动物(犬)原位模型中再生血管化的牙髓样软组织。再生的软组织再现了天然牙髓的关键特征,例如血管、神经丝和紧邻牙本质小管的成牙本质样层。我们的研究确立了血管生成肽水凝胶作为促进体内软组织再生的有效支架。
牙髓组织工程的一个主要挑战是腔内植入物内缺乏原位血管生成,尤其是在牙髓完全切除后。植入物中缺乏强健的脉管系统会限制基质与宿主组织的整合以及软组织的再生。我们在牙髓样软组织再生的临床前犬模型中证明了一种无需添加生长因子即可促进体内组织再血管化的无细胞材料的开发。这种无细胞生物材料将促进大型动物模型中的牙髓再血管化方法,并转化为人类临床试验。