首页> 外文期刊>Tissue engineering, Part A >Coadministration of platelet-derived growth factor-BB and vascular endothelial growth factor with bladder acellular matrix enhances smooth muscle regeneration and vascularization for bladder augmentation in a rabbit model
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Coadministration of platelet-derived growth factor-BB and vascular endothelial growth factor with bladder acellular matrix enhances smooth muscle regeneration and vascularization for bladder augmentation in a rabbit model

机译:血小板源性生长因子-BB和血管内皮生长因子与膀胱脱细胞基质的共同给药可增强平滑肌再生和血管生成,从而增强兔模型中的膀胱

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摘要

Tissue-engineering techniques have brought a great hope for bladder repair and reconstruction. The crucial requirements of a tissue-engineered bladder are bladder smooth muscle regeneration and vascularization. In this study, partial rabbit bladder (4×5 cm) was removed and replaced with a porcine bladder acellular matrix (BAM) that was equal in size. BAM was incorporated with platelet-derived growth factor-BB (PDGF-BB) and vascular endothelial growth factor (VEGF) in the experimental group while with no bioactive factors in the control group. The bladder tissue strip contractility in the experimental rabbits was better than that in the control ones postoperation. Histological evaluation revealed that smooth muscle regeneration and vascularization in the experimental group were significantly improved compared with those in the control group (p<0.05), while multilayered urothelium was formed in both groups. Muscle strip contractility of neobladder in the experimental group exhibited significantly better than that in the control (p<0.05) assessed with electrical field stimulation and carbachol interference. The activity of matrix metalloproteinase-2 (MMP-2) and MMP-9 in the native bladder tissue around tissue-engineered neobladder in the experimental group was significantly higher than that in the control (p<0.05). This work suggests that smooth muscle regeneration and vascularization in tissue-engineered neobladder and recovery of bladder function could be enhanced by PDGF-BB and VEGF incorporated within BAM, which promoted the upregulation of the activity of MMP-2 and MMP-9 of native bladder tissue around the tissue-engineered neobladder.
机译:组织工程技术为膀胱修复和重建带来了巨大希望。组织工程膀胱的关键要求是膀胱平滑肌再生和血管形成。在这项研究中,切除了部分兔膀胱(4×5 cm),并用大小相等的猪膀胱无细胞基质(BAM)代替。在实验组中,BAM与血小板源性生长因子-BB(PDGF-BB)和血管内皮生长因子(VEGF)结合,而对照组中无生物活性因子。实验兔的膀胱组织条带收缩力好于对照组。组织学评估显示,与对照组相比,实验组的平滑肌再生和血管形成显着改善(p <0.05),而两组均形成了多层尿路上皮。用电场刺激和卡巴胆碱干扰评估,实验组新膀胱的肌肉条收缩性明显优于对照组(p <0.05)。实验组组织工程化新膀胱周围天然膀胱组织中基质金属蛋白酶2(MMP-2)和MMP-9的活性显着高于对照组(p <0.05)。这项工作表明,通过在BAM中掺入PDGF-BB和VEGF可以增强组织工程新膀胱中平滑肌的再生和血管形成以及膀胱功能的恢复,从而促进天然膀胱MMP-2和MMP-9活性的上调组织工程化的新膀胱周围的组织。

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