4.8 Article

Angiogenic hydrogels for dental pulp revascularization

Journal

ACTA BIOMATERIALIA
Volume 126, Issue -, Pages 109-118

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.actbio.2021.03.001

Keywords

Self-assembly; Angiogenesis; Acellular scaffolds; Tissue regeneration; Pulp revascularization

Funding

  1. NJIT
  2. NJIT Undergraduate Research and Innovation (URI) program
  3. National Eye Institute NIH [R15 EY029504]
  4. National Science Foundation NSF [IIP 1903617]
  5. NIH [R01DE025885, R01 AR072731]

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The study demonstrates the potential of acellular self-assembling peptide hydrogels in promoting tissue revascularization and soft tissue regeneration after endodontic treatment. The hydrogels show promise in guiding the development of neovasculature and tissue deposition, providing a scaffold for soft tissue regeneration in vivo.
Angiogenesis is critical for tissue healing and regeneration. Promoting angiogenesis in materials im -planted within dental pulp after pulpectomy is a major clinical challenge in endodontics. We demon-strate 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 pos-sess 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) ortho-topic 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 im -plants 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 bioma-terials would facilitate pulp revascularization approaches in large animal models, and translation into human clinical trials. (c) 2021 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.

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