Bioengineered bladder patches constructed from multilayered adipose-derived stem cell sheets for bladder regeneration

被引:28
作者
Wang, Ying [1 ]
Zhou, Shukui [1 ]
Yang, Ranxing [1 ]
Zou, Qingsong [1 ]
Zhang, Kaile [1 ]
Tian, Qinghua [2 ]
Zhao, Weixin [3 ]
Zong, Lijuan [4 ]
Fu, Qiang [1 ]
机构
[1] Shanghai Jiao Tong Univ, Dept Urol, Affiliated Peoples Hosp 6, Shanghai Eastern Inst Urol Reconstruct, Shanghai 200233, Peoples R China
[2] Shanghai Jiao Tong Univ, Dept Radiol, Affiliated Peoples Hosp 6, Shanghai 200233, Peoples R China
[3] Wake Forest Inst Regenerat Med, Winston Salem, NC USA
[4] Shanghai Key Lab Tissue Engn, Shanghai 200011, Peoples R China
基金
中国国家自然科学基金;
关键词
Bladder regeneration; Adipose-derived stem cell; Cell sheet; Ultrasmall super-paramagnetic iron oxide; Tissue engineering; ACELLULAR MATRIX GRAFT; SILK FIBROIN SCAFFOLDS; TISSUE REGENERATION; VASCULAR GRAFTS; URINARY-BLADDER; RECONSTRUCTION; AUGMENTATION; TRANSPLANTATION; FRAGMENTS; CHILDREN;
D O I
10.1016/j.actbio.2018.12.016
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Cell-seeded scaffolds are a common route of cell transplantation for bladder repair and reconstruction. However, when cell suspensions are harvested, proteolytic enzymes often cause extracellular matrix damage and loss of intercellular junctions. To overcome this problem, we developed a bioengineered three-dimensional bladder patch comprising porous scaffolds and multilayered adipose-derived stem cell (ASC) sheets, and evaluated its feasibility for bladder regeneration in a rat model. Adipose-derived stem cells (ASCs) were labeled with ultrasmall super-paramagnetic iron oxide (USPIO) nanoparticles. ASC patches were constructed using multilayered USPIO-labeled ASC sheets and porous polyglycolic acid scaffolds. To monitor the distribution and localization of bioengineered bladder patches in live animals, magnetic resonance imaging (MRI) was performed 2 weeks, 4 weeks and 8 weeks after transplantation. The bladder regenerative potential of ASC patches was further evaluated by urodynamic and histological analysis. Scanning electron microscopy indicated that cell sheets adhered tightly to the scaffold. MRI showed hypointense signals that lasted up to 8 weeks at the site of USPIO-labeled ASC sheet transplants. Immunofluorescence demonstrated that these tissue-engineered bladder patches promoted regeneration of urothelium, smooth muscle, neural cells and blood vessels. Urodynamic testing revealed that the ASC patch restored bladder function with augmented capacity. The USPIO-labeled ASC patch provides a promising perspective on image-guided tissue engineering and holds great promise as a safe and effective therapeutic strategy for bladder regeneration. Statement of Significance Adipose-derived stem cell (ASC) sheets avoid enzymatic dissociation and preserve the cell-to-cell interactions and extracellular matrix (ECM) proteins, which exhibit great potential for tissue regeneration. In this study, we developed a bioengineered three-dimensional bladder patch comprising porous scaffolds and multilayered ASC sheets, and evaluated its feasibility for bladder regeneration in a rat model. Tissue-engineered bladder patches restored bladder function and promoted regeneration of urothelium, smooth muscle, neural cells and blood vessels. Moreover, ultrasmall super-paramagnetic iron oxide (USPIO)-labeled bladder patches can be dynamically monitored in vivo by noninvasive MRI for long periods of time. Therefore, The USPIO-labeled bladder patch provides a promising image-guided therapeutic strategy for bladder regeneration. (C) 2018 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:131 / 141
页数:11
相关论文
共 41 条
[1]   Engineered small diameter vascular grafts by combining cell sheet engineering and electrospinning technology [J].
Ahn, Hyunhee ;
Ju, Young Min ;
Takahashi, Hironobu ;
Williams, David F. ;
Yoo, James J. ;
Lee, Sang Jin ;
Okano, Teruo ;
Atala, Anthony .
ACTA BIOMATERIALIA, 2015, 16 :14-22
[2]   Tissue-engineered autologous bladders for patients needing cystoplasty [J].
Atala, A ;
Bauer, SB ;
Soker, S ;
Yoo, JJ ;
Retik, AB .
LANCET, 2006, 367 (9518) :1241-1246
[3]   The promotion of functional urinary bladder regeneration using anti-inflammatory nanofibers [J].
Bury, Matthew I. ;
Fuller, Natalie J. ;
Meisner, Jay W. ;
Hofer, Matthias D. ;
Webber, Matthew J. ;
Chow, Lesley W. ;
Prasad, Sheba ;
Thaker, Hatim ;
Yue, Xuan ;
Menon, Vani S. ;
Diaz, Edward C. ;
Stupp, Samuel I. ;
Cheng, Earl Y. ;
Sharma, Arun K. .
BIOMATERIALS, 2014, 35 (34) :9311-9321
[4]   The Current Use of Stem Cells in Bladder Tissue Regeneration and Bioengineering [J].
Chan, Yvonne Y. ;
Sandlin, Samantha K. ;
Kurzrock, Eric A. ;
Osborn, Stephanie L. .
BIOMEDICINES, 2017, 5 (01)
[5]   Bladder tissue-engineering: a new practical solution? [J].
Chung, SY .
LANCET, 2006, 367 (9518) :1215-1216
[6]   The use of bi-layer silk fibroin scaffolds and small intestinal submucosa matrices to support bladder tissue regeneration in a rat model of spinal cord injury [J].
Chung, Yeun Goo ;
Algarrahi, Khalid ;
Franck, Debra ;
Tu, Duong D. ;
Adam, Rosalyn M. ;
Kaplan, David L. ;
Estrada, Carlos R., Jr. ;
Mauney, Joshua R. .
BIOMATERIALS, 2014, 35 (26) :7452-7459
[7]   Bladder reconstruction: The past, present and future [J].
El-Taji, Omar M. S. ;
Khattak, Altaf Q. ;
Hussain, Syed A. .
ONCOLOGY LETTERS, 2015, 10 (01) :3-10
[8]   Comparison of SPIO and USPIO for in vitro labeling of human monocytes:: MR detection and cell function [J].
Engberink, Raoul D. Oude ;
van der Pol, Susanne M. A. ;
Dopp, Ed A. ;
de Vries, Helga E. ;
Blezer, Erwin L. A. .
RADIOLOGY, 2007, 243 (02) :467-474
[9]   Metabolic consequences and long-term complications of enterocystoplasty in children: A review [J].
Gilbert, SM ;
Hensle, TW .
JOURNAL OF UROLOGY, 2005, 173 (04) :1080-1086
[10]   Ultrastructural characterization of mesenchymal stromal cells labeled with ultrasmall superparamagnetic iron-oxide nanoparticles for clinical tracking studies [J].
Hansen, Louise ;
Hansen, Alastair B. ;
Mathiasen, Anders B. ;
Ng, Michael ;
Bhakoo, Kishore ;
Ekblond, Annette ;
Kastrup, Jens ;
Friis, Tina .
SCANDINAVIAN JOURNAL OF CLINICAL & LABORATORY INVESTIGATION, 2014, 74 (05) :437-446