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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 |
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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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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.</description><identifier>ISSN: 0109-5641</identifier><identifier>EISSN: 1879-0097</identifier><identifier>DOI: 10.1016/j.dental.2022.09.011</identifier><identifier>PMID: 36180310</identifier><language>eng</language><publisher>England: Elsevier Inc</publisher><subject>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</subject><ispartof>Dental materials, 2022-11, Vol.38 (11), p.1749-1762</ispartof><rights>2022 Elsevier Inc.</rights><rights>Copyright © 2022 Elsevier Inc. All rights reserved.</rights><rights>Copyright Elsevier BV Nov 2022</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4061-1ba94a8a42a2a174f0f693ac9863510ddf9f1ab7820ed545a60ae01b06d3e3023</citedby><cites>FETCH-LOGICAL-c4061-1ba94a8a42a2a174f0f693ac9863510ddf9f1ab7820ed545a60ae01b06d3e3023</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,777,781,882,27905,27906</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36180310$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>de Souza Araújo, Isaac J.</creatorcontrib><creatorcontrib>Ferreira, Jessica A.</creatorcontrib><creatorcontrib>Daghrery, Arwa</creatorcontrib><creatorcontrib>Ribeiro, Juliana S.</creatorcontrib><creatorcontrib>Castilho, Miguel</creatorcontrib><creatorcontrib>Puppin-Rontani, Regina M.</creatorcontrib><creatorcontrib>Bottino, Marco C.</creatorcontrib><title>Self-assembling peptide-laden electrospun scaffolds for guided mineralized tissue regeneration</title><title>Dental materials</title><addtitle>Dent Mater</addtitle><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.</description><subject>Animals</subject><subject>Apatite</subject><subject>Apatites</subject><subject>Biocompatibility</subject><subject>Biocompatible Materials</subject><subject>Biomaterials</subject><subject>Biomedical materials</subject><subject>Biomineralization</subject><subject>Biomolecules</subject><subject>Body fluids</subject><subject>Bone growth</subject><subject>Bone Regeneration</subject><subject>Calvaria</subject><subject>Crystal defects</subject><subject>Crystallization</subject><subject>Dental caries</subject><subject>Dental enamel</subject><subject>Dental materials</subject><subject>Electrospinning</subject><subject>Extracellular matrix</subject><subject>Fibrous structure</subject><subject>Functional groups</subject><subject>Gene expression</subject><subject>Humans</subject><subject>In vivo methods and tests</subject><subject>Mineralization</subject><subject>Nanofibers - chemistry</subject><subject>Peptides</subject><subject>Polyesters - chemistry</subject><subject>Rats</subject><subject>Regeneration</subject><subject>Regeneration (physiology)</subject><subject>Scaffolds</subject><subject>Scaffolds, Self-assembling peptide</subject><subject>Self-assembly</subject><subject>Stem cell transplantation</subject><subject>Stem cells</subject><subject>Teeth</subject><subject>Tissue engineering</subject><subject>Tissue Engineering - methods</subject><subject>Tissue Scaffolds - chemistry</subject><subject>Tissues</subject><issn>0109-5641</issn><issn>1879-0097</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNp9kU9r3DAQxUVpabZJv0EIhp7tzsiybF0CJaR_INBD22uEbI02WryWI9mB9tNXy6ZJe-lJQnrz5vF-jJ0jVAgo3-8qS9NixooD5xWoChBfsA12rSoBVPuSbQBBlY0UeMLepLQDAMEVvmYntcQOaoQNu_1GoytNSrTvRz9ti5nmxVsqR5PtCxppWGJI8zoVaTDOhdGmwoVYbNesssXeTxTN6H_l--JTWqmItKXD4-LDdMZeOTMmevt4nrIfH6-_X30ub75--nL14aYcBEgssTdKmM4IbrjBVjhwUtVmUJ2sGwRrnXJo-rbjQLYRjZFgCLAHaWuqgden7PLoO6_9nuyQm8mp9Bz93sSfOhiv__2Z_J3ehgetug5lp7LBu0eDGO5XSovehTVOObPmbd4olGpEVomjasidpEjuaQOCPlDRO32kog9UNCidqeSxi7_TPQ39wfAcn3JHD56iToOnaSDrYwagbfD_3_AbeYyiXQ</recordid><startdate>20221101</startdate><enddate>20221101</enddate><creator>de Souza Araújo, Isaac J.</creator><creator>Ferreira, Jessica A.</creator><creator>Daghrery, Arwa</creator><creator>Ribeiro, Juliana S.</creator><creator>Castilho, Miguel</creator><creator>Puppin-Rontani, Regina M.</creator><creator>Bottino, Marco C.</creator><general>Elsevier Inc</general><general>Elsevier BV</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QF</scope><scope>7QO</scope><scope>7QP</scope><scope>7QQ</scope><scope>7SC</scope><scope>7SE</scope><scope>7SP</scope><scope>7SR</scope><scope>7TA</scope><scope>7TB</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>F28</scope><scope>FR3</scope><scope>H8D</scope><scope>H8G</scope><scope>JG9</scope><scope>JQ2</scope><scope>K9.</scope><scope>KR7</scope><scope>L7M</scope><scope>L~C</scope><scope>L~D</scope><scope>P64</scope><scope>5PM</scope></search><sort><creationdate>20221101</creationdate><title>Self-assembling peptide-laden electrospun scaffolds for guided mineralized tissue regeneration</title><author>de Souza Araújo, Isaac J. ; 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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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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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