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Self-assembling peptide-laden electrospun scaffolds for guided mineralized tissue regeneration

Electrospun scaffolds are a versatile biomaterial platform to mimic fibrillar structure of native tissues extracellular matrix, and facilitate the incorporation of biomolecules for regenerative therapies. Self-assembling peptide P11-4 has emerged as a promising strategy to induce mineralization; how...

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Published in:Dental materials 2022-11, Vol.38 (11), p.1749-1762
Main Authors: de Souza Araújo, Isaac J., Ferreira, Jessica A., Daghrery, Arwa, Ribeiro, Juliana S., Castilho, Miguel, Puppin-Rontani, Regina M., Bottino, Marco C.
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cited_by cdi_FETCH-LOGICAL-c4061-1ba94a8a42a2a174f0f693ac9863510ddf9f1ab7820ed545a60ae01b06d3e3023
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creator de Souza Araújo, Isaac J.
Ferreira, Jessica A.
Daghrery, Arwa
Ribeiro, Juliana S.
Castilho, Miguel
Puppin-Rontani, Regina M.
Bottino, Marco C.
description Electrospun scaffolds are a versatile biomaterial platform to mimic fibrillar structure of native tissues extracellular matrix, and facilitate the incorporation of biomolecules for regenerative therapies. Self-assembling peptide P11-4 has emerged as a promising strategy to induce mineralization; however, P11-4 application has been mostly addressed for early caries lesions repair on dental enamel. Here, to investigate P11-4′s efficacy on bone regeneration, polymeric electrospun scaffolds were developed, and then distinct concentrations of P11-4 were physically adsorbed on the scaffolds. P11-4-laden and pristine (P11-4-free) electrospun scaffolds were immersed in simulated body fluid and mineral precipitation identified by SEM. Functional groups and crystalline phases were analyzed by FTIR and XRD, respectively. Cytocompatibility, mineralization, and gene expression assays were conducted using stem cells from human exfoliated deciduous teeth. To investigate P11-4-laden scaffolds potential to induce in vivo mineralization, an established rat calvaria critical-size defect model was used. Results. We successfully synthesized nanofibrous (∼ 500 nm fiber diameter) scaffolds and observed that functionalization with P11-4 did not affect the fibers’ diameter. SEM images indicated mineral precipitation, while FTIR and XRD confirmed apatite-like formation and crystallization for P11-4-laden scaffolds. In addition, P11-4-laden scaffolds were cytocompatible, highly stimulated cell-mediated mineral deposition, and upregulated the expression of mineralization-related genes compared to pristine scaffolds. P11-4-laden scaffolds led to enhanced in vivo bone regeneration after 8 weeks compared to pristine PCL. Electrospun scaffolds functionalized with P11-4 are a promising strategy for inducing mineralized tissues regeneration in the craniomaxillofacial complex. [Display omitted] •Self-assembly peptide P11-4-laden scaffolds induces mineral precipitation.•P11-4-laden scaffolds stimulate stem cells to mineral deposition.•P11-4-laden scaffolds upregulate osteogenic markers.•P11-4-laden scaffolds induces bone formation in vivo.
doi_str_mv 10.1016/j.dental.2022.09.011
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We successfully synthesized nanofibrous (∼ 500 nm fiber diameter) scaffolds and observed that functionalization with P11-4 did not affect the fibers’ diameter. SEM images indicated mineral precipitation, while FTIR and XRD confirmed apatite-like formation and crystallization for P11-4-laden scaffolds. In addition, P11-4-laden scaffolds were cytocompatible, highly stimulated cell-mediated mineral deposition, and upregulated the expression of mineralization-related genes compared to pristine scaffolds. P11-4-laden scaffolds led to enhanced in vivo bone regeneration after 8 weeks compared to pristine PCL. Electrospun scaffolds functionalized with P11-4 are a promising strategy for inducing mineralized tissues regeneration in the craniomaxillofacial complex. 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We successfully synthesized nanofibrous (∼ 500 nm fiber diameter) scaffolds and observed that functionalization with P11-4 did not affect the fibers’ diameter. SEM images indicated mineral precipitation, while FTIR and XRD confirmed apatite-like formation and crystallization for P11-4-laden scaffolds. In addition, P11-4-laden scaffolds were cytocompatible, highly stimulated cell-mediated mineral deposition, and upregulated the expression of mineralization-related genes compared to pristine scaffolds. P11-4-laden scaffolds led to enhanced in vivo bone regeneration after 8 weeks compared to pristine PCL. Electrospun scaffolds functionalized with P11-4 are a promising strategy for inducing mineralized tissues regeneration in the craniomaxillofacial complex. 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Self-assembling peptide P11-4 has emerged as a promising strategy to induce mineralization; however, P11-4 application has been mostly addressed for early caries lesions repair on dental enamel. Here, to investigate P11-4′s efficacy on bone regeneration, polymeric electrospun scaffolds were developed, and then distinct concentrations of P11-4 were physically adsorbed on the scaffolds. P11-4-laden and pristine (P11-4-free) electrospun scaffolds were immersed in simulated body fluid and mineral precipitation identified by SEM. Functional groups and crystalline phases were analyzed by FTIR and XRD, respectively. Cytocompatibility, mineralization, and gene expression assays were conducted using stem cells from human exfoliated deciduous teeth. To investigate P11-4-laden scaffolds potential to induce in vivo mineralization, an established rat calvaria critical-size defect model was used. Results. We successfully synthesized nanofibrous (∼ 500 nm fiber diameter) scaffolds and observed that functionalization with P11-4 did not affect the fibers’ diameter. SEM images indicated mineral precipitation, while FTIR and XRD confirmed apatite-like formation and crystallization for P11-4-laden scaffolds. In addition, P11-4-laden scaffolds were cytocompatible, highly stimulated cell-mediated mineral deposition, and upregulated the expression of mineralization-related genes compared to pristine scaffolds. P11-4-laden scaffolds led to enhanced in vivo bone regeneration after 8 weeks compared to pristine PCL. Electrospun scaffolds functionalized with P11-4 are a promising strategy for inducing mineralized tissues regeneration in the craniomaxillofacial complex. [Display omitted] •Self-assembly peptide P11-4-laden scaffolds induces mineral precipitation.•P11-4-laden scaffolds stimulate stem cells to mineral deposition.•P11-4-laden scaffolds upregulate osteogenic markers.•P11-4-laden scaffolds induces bone formation in vivo.</abstract><cop>England</cop><pub>Elsevier Inc</pub><pmid>36180310</pmid><doi>10.1016/j.dental.2022.09.011</doi><tpages>14</tpages><oa>free_for_read</oa></addata></record>
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source ScienceDirect Freedom Collection 2022-2024
subjects Animals
Apatite
Apatites
Biocompatibility
Biocompatible Materials
Biomaterials
Biomedical materials
Biomineralization
Biomolecules
Body fluids
Bone growth
Bone Regeneration
Calvaria
Crystal defects
Crystallization
Dental caries
Dental enamel
Dental materials
Electrospinning
Extracellular matrix
Fibrous structure
Functional groups
Gene expression
Humans
In vivo methods and tests
Mineralization
Nanofibers - chemistry
Peptides
Polyesters - chemistry
Rats
Regeneration
Regeneration (physiology)
Scaffolds
Scaffolds, Self-assembling peptide
Self-assembly
Stem cell transplantation
Stem cells
Teeth
Tissue engineering
Tissue Engineering - methods
Tissue Scaffolds - chemistry
Tissues
title Self-assembling peptide-laden electrospun scaffolds for guided mineralized tissue regeneration
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