Tissue engineering of bladder using vascular endothelial growth factor gene-modified endothelial progenitor cells

被引:29
作者
Chen, Bai-Song [1 ]
Xie, Hua [1 ]
Zhang, Sheng-Li [1 ]
Geng, Hong-Quan [2 ]
Zhou, Jun-Mei [1 ]
Pan, Jun [2 ]
Chen, Fang [1 ]
机构
[1] Shanghai Jiao Tong Univ, Dept Urol, Shanghai Childrens Hosp, Childrens Hosp, Shanghai 200040, Peoples R China
[2] Shanghai Jiao Tong Univ, Dept Urol, Xinhua Hosp, Sch Med, Shanghai 200040, Peoples R China
基金
中国国家自然科学基金;
关键词
Bladder; Endothelial progenitor cells (EPCs); Gene therapy; Tissue engineering; Vascular endothelial growth factor (VEGF); THERAPEUTIC NEOVASCULARIZATION; ACELLULAR MATRIX; MUSCLE-CELLS; CORD BLOOD; IN-VITRO; TRANSPLANTATION; ANGIOGENESIS; REGENERATION; ENHANCEMENT; RELEASE;
D O I
10.5301/ijao.5000069
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Purpose: This study assessed the use of vascular endothelial growth factor (VEGF) gene-modified endothelial progenitor cells (EPCs) seeded onto bladder acellular matrix grafts (BAMGs), to enhance the blood supply in tissue-engineered bladders in a porcine model. Methods: Autologous porcine peripheral EPCs were isolated, cultured, expanded, characterized, and modified with the VEGF gene using an adenovirus vector. The expression of VEGF was examined using reverse transcriptase polymerase chain reaction (RT-PCR) and an enzyme-linked immunosorbent assay (ELISA). VEGF gene modified EPCs were seeded onto BAMG and cultured for 3 days before implantation into pigs for bladder tissue engineering. A partial bladder cystectomy was performed in 12 pigs. The experimental group (6 pigs) received VEGF gene-modified EPC-seeded BAMG. The control group (6 pigs) received BAMG without seeded EPCs. The resulting tissue-engineered bladders were subject to a general and histological analysis. Microvessel density (MVD) was assessed using immunohistochemistry. Results: The ex vivo transfection efficiency of EPCs was greater than 60%-70% when concentrated adenovirus was used. The genetically modified cells expressed both VEGF and Green Fluorescent Protein (GFP). Scanning electron microscopy (SEM) and Masson's trichrome staining of cross sections of the cultured cells seeded to BAMG showed cell attachment and proliferation on the surface of the BAMG. Histological examination revealed bladder regeneration in a time-dependent fashion. Significant increases in MVD were observed in the experimental group, in comparison with the control group. Conclusions: VEGF-modified EPCs significantly enhanced neovascularization, compared with BAMG alone. These results indicate that EPCs, combined with VEGF gene therapy, may be a suitable approach for increasing blood supply in the tissue engineering of bladders. Thus, a useful strategy to achieve a tissue-engineered bladder is indicated.
引用
收藏
页码:1137 / 1146
页数:10
相关论文
共 27 条
[1]   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
[2]   Tissue engineering in urologic surgery [J].
Atala, A .
UROLOGIC CLINICS OF NORTH AMERICA, 1998, 25 (01) :39-+
[3]   Tissue engineering of human bladder [J].
Atala, Anthony .
BRITISH MEDICAL BULLETIN, 2011, 97 (01) :81-104
[4]   22 week assessment of bladder acellular matrix as a bladder augmentation material in a porcine model [J].
Brown, AL ;
Farhat, W ;
Merguerian, PA ;
Wilson, GJ ;
Khoury, AE ;
Woodhouse, KA .
BIOMATERIALS, 2002, 23 (10) :2179-2190
[5]   Acellular collagen matrix as a possible "off the shelf" biomaterial for urethral repair [J].
Chen, F ;
Yoo, JJ ;
Atala, A .
UROLOGY, 1999, 54 (03) :407-410
[6]   Angiogenic gene-modified muscle cells for enhancement of tissue formation [J].
De Coppi, P ;
Delo, D ;
Farrugia, L ;
Udompanyanan, K ;
Yoo, JJ ;
Nomi, M ;
Atala, A ;
Soker, S .
TISSUE ENGINEERING, 2005, 11 (7-8) :1034-1044
[7]   Angiogenic gene modification of skeletal muscle cells to compensate for ageing-induced decline in bioengineered functional muscle tissue [J].
Delo, Dawn M. ;
Eberli, Daniel ;
Williams, J. Koudy ;
Andersson, Karl-Erik ;
Atala, Anthony ;
Soker, Shay .
BJU INTERNATIONAL, 2008, 102 (07) :878-884
[8]   Molecular and cellular regulators of cancer angiogenesis [J].
Goh, P. P. ;
Sze, D. M. ;
Roufogalis, B. D. .
CURRENT CANCER DRUG TARGETS, 2007, 7 (08) :743-758
[9]   Tissue engineering of urethra using human vascular endothelial growth factor gene-modified bladder urothelial cells [J].
Guan, Yong ;
Ou, Lailiang ;
Hu, Gang ;
Wang, Hongjun ;
Xu, Yong ;
Chen, Jiatong ;
Zhang, Jun ;
Yu, Yaoting ;
Kong, Deling .
ARTIFICIAL ORGANS, 2008, 32 (02) :91-99
[10]   Identification of a novel hierarchy of endothelial progenitor cells using human peripheral and umbilical cord blood [J].
Ingram, DA ;
Mead, LE ;
Tanaka, H ;
Meade, V ;
Fenoglio, A ;
Mortell, K ;
Pollok, K ;
Ferkowicz, MJ ;
Gilley, D ;
Yoder, MC .
BLOOD, 2004, 104 (09) :2752-2760