Biomimetic scaffold containing PVDF nanofibers with sustained TGF-β release in combination with AT-MSCs for bladder tissue engineering

被引:31
作者
Ardeshirylajimi, Abdolreza [1 ,2 ]
Ghaderian, Sayyed Mohammad-Hossein [1 ,3 ]
Omrania, Mir Davood [1 ,3 ]
Moradi, Sadegh Lotfalah [2 ]
机构
[1] Shahid Beheshti Univ Med Sci, Urogenital Stem Cell Res Ctr, 23 Shahid LabbafiNejad Educ Hosp,Amir Ebrahimi St, Tehran, Iran
[2] Shahid Beheshti Univ Med Sci, Sch Adv Technol Med, Dept Tissue Engn & Appl Cell Sci, Tehran, Iran
[3] Shahid Beheshti Univ Med Sci, Fac Med, Dept Med Genet, Tehran, Iran
关键词
Poly (vinylidene fluoride); Mesenchymal stem cells; Bladder tissue engineering; TGF beta; MESENCHYMAL STEM-CELLS; SMOOTH-MUSCLE-CELL; SPINAL-CORD-INJURY; NEUROGENIC BLADDER; GROWTH-FACTOR; RAT MODEL; DIFFERENTIATION; AUGMENTATION; REGENERATION; CYSTOPLASTY;
D O I
10.1016/j.gene.2018.07.046
中图分类号
Q3 [遗传学];
学科分类号
071007 [遗传学];
摘要
Since the functional recovery of the reconstructed bladder is related to the bladder wall contraction and existing therapies do not respond to this, tissue engineering could be worth considered promising candidates for developing of conventional treatments in these kinds of ailments. Due to the low mechanical properties of natural scaffolds, biocompatible synthetic scaffolds can play a key role in the stem cells proliferation and differentiation and apply for many tissue-engineering applications. On the other hand, considering the low shelf life of TGF beta, encapsulating this growth factor can help maintain its functionality throughout the study period. In this study, poly (vinylidene fluoride) (PVDF) nanofibrous scaffolds were fabricated through electrospinning method with or without chitosan nanoparticles loaded TGF beta. All scaffolds characterized morphologically by using SEM, TGF beta release profiling as well as biocompatibility by using SEM and MTT assays. Adipose tissue derived mesenchymal stem cells (AT-MSCs) was isolated and characterized immediately and the differentiation of SMC was investigated when cultured on the surface of the scaffolds and tissue culture polystyrene (TCPS) as a control of gene and protein expression levels. Fabricated scaffold possess smooth structure with nanoscale size and long time releasing of sustained profiles. MTT, qRT-PCR and immunocytochemistry results demonstrated that AT-MSCs proliferation rate and SMC differentiation potential were significantly increased when cultured on the PVDF-TGF beta scaffold in comparison with PVDF and TCPS. According to the results, PVDF-TGF beta as a bio-functional scaffold can provide greater treatment possibilities in bladder tissue engineering applications.
引用
收藏
页码:195 / 201
页数:7
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