| Literature DB >> 34256231 |
Vincent Fitzpatrick1, Zaira Martín-Moldes1, Anna Deck1, Ruben Torres-Sanchez1, Anne Valat1, Dana Cairns1, Chunmei Li1, David L Kaplan2.
Abstract
Our goal was to generate functionalized 3D-printed scaffolds for bone regeneration using silk-hydroxyapatite bone cements and osteoinductive, proangiogenic and neurotrophic growth factors or morphogens for accelerated bone formation. 3D printing was utilized to generate macroporous scaffolds with controlled geometries and architectures that promote osseointegration. We build on the knowledge that the osteoinductive factor Bone Morphogenetic Protein-2 (BMP2) can also positively impact vascularization, Vascular Endothelial Growth Factor (VEGF) can impact osteoblastic differentiation, and that Neural Growth Factor (NGF)-mediated signaling can influence bone regeneration. We assessed functions on the 3D printed construct via the osteogenic differentiation of human mesenchymal stem cells; migration and proliferation of human umbilical vein endothelial cells; and proliferation of human induced neural stem cells. The scaffolds provided mechanical properties suitable for bone and the materials were cytocompatible, osteoconductive and maintained the activity of the morphogens and cytokines. Synergistic outcomes between BMP-2, VEGF and NGF in terms of osteoblastic differentiation in vitro were identified, based on the upregulation of genes associated with osteoblastic differentiation (Runt-related transcription factor-2, Osteopontin, Bone Sialoprotein). Additional studies will be required to assess these scaffold designs in vivo. These results are expected to have a strong impact in bone regeneration in dental, oral and maxillofacial surgery.Entities:
Keywords: 3D printing; Bone regeneration; Innervation; Silk; Tissue engineering; Vascularization
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Year: 2021 PMID: 34256231 PMCID: PMC8408341 DOI: 10.1016/j.biomaterials.2021.120995
Source DB: PubMed Journal: Biomaterials ISSN: 0142-9612 Impact factor: 15.304