In vivo comparison of biomimetic approaches for tissue regeneration of the scarred vocal fold.
In vivo comparison of biomimetic approaches for tissue regeneration of the scarred vocal fold.
复制标题
疤痕声带组织再生仿生方法的体内比较。
DOI:
10.1089/ten.tea.2008.0299
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发表时间:
2009
影响因子:
--
通讯作者:
Prestwich,Glenn
中科院分区:
文献类型:
--
作者:
Thibeault,SusanL;Klemuk,SarahA;Smith,MarshallE;Leugers,Cecilia;Prestwich,Glenn
The objective of this study was to determine if three different biomimetic approaches could facilitate tissue regeneration and improve viscoelastic properties in the scarred vocal fold lamina propria extracellular matrix (ECM). Twenty rabbit vocal folds were biopsied bilaterally; 2 months postinjury rabbits were unilaterally treated with (i) autologous fibroblasts, (ii) a semisynthetic ECM (sECM), or (iii) autologous fibroblasts encapsulated in sECM. Saline was injected as a control into the contralateral fold. Animals were sacrificed 2 months after treatment. Outcomes measured were procollagen, collagen, and fibronectin levels in the lamina propria, and tissue viscosity and elasticity across three frequency decades. All treatment groups demonstrated accelerated proliferation of the ECM. Vocal fold lamina propria treated with autologous fibroblasts were found to have significantly improved viscosity (p= 0.0077) and elasticity (p= 0.0081) compared to saline. This treatment group had significantly elevated fibronectin levels. sECM and autologous fibroblasts/sECM groups had significantly elevated levels of procollagen, collagen, and fibronectin, indicating abundant matrix production as compared to saline with viscoelastic measures that did not differ statistically from controls. The use of autologous fibroblasts led to better restoration of the vocal fold lamina propria biomechanical properties. Optimization of cell–scaffold interactions and subsequent cell behavior is necessary for utilization of scaffold and scaffold–cell approaches.
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影响因子:
2.2
作者:
Thibeault, SL;Gray, SD;Ford, CN
通讯作者:
Ford, CN
影响因子:
6.2
作者:
Shu, XZ;Liu, YC;Prestwich, GD
通讯作者:
Prestwich, GD
影响因子:
14
作者:
Liu, YC;Shu, XZ;Prestwich, GD
通讯作者:
Prestwich, GD
影响因子:
--
作者:
Prestwich,GlennD;Shu,XiaoZheng;Liu,Yanchun;Cai,Shenshen;Walsh,JenniferF;Hughes,CaseyW;Ahmad,Shama;Kirker,KellyR;Yu,Bolan;Orlandi,RichardR;Park,AlbertH;Thibeault,SusanL;Duflo,Suzy;Smith,MarshallE
通讯作者:
Smith,MarshallE
DOI:
10.1002/jbm.a.31921
发表时间:
2009
期刊:
Journal of biomedical materials research. Part A
影响因子:
--
作者:
Roychowdhury,Priyanka;Klemuk,Sarah;Titze,Ingo;Kumar,Vijay
通讯作者:
Kumar,Vijay