Sarah E. Smith, Colten Snider, D. Gilley, Daniel N. Grant, S. Sherman, B. Ulery, D. Grant, S. Grant
{"title":"Homogenized Porcine Extracellular Matrix Derived Injectable Tissue Construct with Gold Nanoparticles for Musculoskeletal Tissue Engineering Applications","authors":"Sarah E. Smith, Colten Snider, D. Gilley, Daniel N. Grant, S. Sherman, B. Ulery, D. Grant, S. Grant","doi":"10.4236/JBNB.2017.82009","DOIUrl":null,"url":null,"abstract":"A unique porcine extracellular matrix (ECM) derived \ninjectable tissue construct with 100 nm or 20 nm gold nanoparticles (AuNP) was \ndeveloped for musculoskeletal tissue engineering applications. ECM has been \nshown to encourage cellularity and tissue remodeling due to its release of \ngrowth factors while AuNP have been shown to reduce reactive oxygen species \n(ROS) levels. Injectable tissue constructs were created by homogenizing \ndecellularized porcine diaphragm tendon conjugated with 100 nm or 20 nm AuNP at \n1x, 4x, and 8x concentrations. Extrusion force testing demonstrated that \nhomogenized tissue constructs were injectable at an appropriate cannula size \nand force. L-929 murine fibroblasts were used to measure cell viability, cell \nproliferation, intracellular ROS levels, and cell migration in response to \nconstructs. Enhanced cell viability and proliferation are observed on 1 × 20 nm \nAuNP constructs. ROS assays demonstrate reduced cellular ROS concentrations \nfrom all 20 nm AuNP constructs and from 8 × 100 nm AuNP constructs compared with \nconstructs without nanoparticles. Cellular migration is higher towards 4 × 20 nm \nAuNP constructs compared with constructs \nwithout nanoparticles. Results support the potential use of a porcine ECM \nderived injectable tissue construct with AuNP as an injectable tissue construct \nto reduce inflammation and to promote tissue remodeling in musculoskeletal \ntissue engineering applications.","PeriodicalId":68623,"journal":{"name":"生物材料与纳米技术(英文)","volume":"08 1","pages":"125-143"},"PeriodicalIF":0.0000,"publicationDate":"2017-04-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"13","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"生物材料与纳米技术(英文)","FirstCategoryId":"1089","ListUrlMain":"https://doi.org/10.4236/JBNB.2017.82009","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 13
Abstract
A unique porcine extracellular matrix (ECM) derived
injectable tissue construct with 100 nm or 20 nm gold nanoparticles (AuNP) was
developed for musculoskeletal tissue engineering applications. ECM has been
shown to encourage cellularity and tissue remodeling due to its release of
growth factors while AuNP have been shown to reduce reactive oxygen species
(ROS) levels. Injectable tissue constructs were created by homogenizing
decellularized porcine diaphragm tendon conjugated with 100 nm or 20 nm AuNP at
1x, 4x, and 8x concentrations. Extrusion force testing demonstrated that
homogenized tissue constructs were injectable at an appropriate cannula size
and force. L-929 murine fibroblasts were used to measure cell viability, cell
proliferation, intracellular ROS levels, and cell migration in response to
constructs. Enhanced cell viability and proliferation are observed on 1 × 20 nm
AuNP constructs. ROS assays demonstrate reduced cellular ROS concentrations
from all 20 nm AuNP constructs and from 8 × 100 nm AuNP constructs compared with
constructs without nanoparticles. Cellular migration is higher towards 4 × 20 nm
AuNP constructs compared with constructs
without nanoparticles. Results support the potential use of a porcine ECM
derived injectable tissue construct with AuNP as an injectable tissue construct
to reduce inflammation and to promote tissue remodeling in musculoskeletal
tissue engineering applications.