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AB182. Therapeutic potential of adipose-derived stem cells-based micro-tissues in a postprostatectomy erectile dysfunction rat model

OBJECTIVE: This study aims to investigate the feasibility and mechanism of adipose-derived stem cells (ADSCs)-based micro-tissues (MTs) in the treatment of ED in a rat model of bilateral cavernous nerves (CNs) injury. METHODS: ADSCs labeled with 5-ethynyl-2-deoxyuridine (EdU) were used to generate M...

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Autores principales: Guan, Ruili, Xu, Yongde, Lei, Hongen, Gao, Zhezhu, Xin, Zhongcheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4708702/
http://dx.doi.org/10.3978/j.issn.2223-4683.2015.s182
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author Guan, Ruili
Xu, Yongde
Lei, Hongen
Gao, Zhezhu
Xin, Zhongcheng
author_facet Guan, Ruili
Xu, Yongde
Lei, Hongen
Gao, Zhezhu
Xin, Zhongcheng
author_sort Guan, Ruili
collection PubMed
description OBJECTIVE: This study aims to investigate the feasibility and mechanism of adipose-derived stem cells (ADSCs)-based micro-tissues (MTs) in the treatment of ED in a rat model of bilateral cavernous nerves (CNs) injury. METHODS: ADSCs labeled with 5-ethynyl-2-deoxyuridine (EdU) were used to generate MTs with hanging drop method. Ten Sprague-Dawley (SD) rats underwent sham surgery and intracavernous (IC) injection of phosphate buffer solution (PBS) (the sham group). Another 70 rats underwent bilateral CN crush and were then treated with PBS (n=10, the crush group), dissociated ADSCs (n=30, the ADSCs group), and MTs (n=30, the MTs group), respectively. At day 1, 3, 7, 14 (n=5), and 28 (n=10) postsurgery, specimens were harvested for histology. At day 28, 10 rats in each group were examined for erectile function before tissue harvest. Light microscopy of the dynamic aggregation of the MT, immunohistologic examination of the MTs, the retention and distribution of EdU + ADSCs in the corpus cavernosum (CC), and the penis histological analyses of collagen content, Western blot of functional proteins in MTs, IC pressure recording on CN electrostimulation. RESULTS: Three-day-old MTs became stable and expressed nerve growth factor, vascular endothelial growth factor, C-X-C chemokine receptor type 4, Wnt5a, and collagen IV. More EdU + ADSCs retained in the CC in the MTs group than that in the ADSCs group. IC injection of MTs resulted in significant restoration of the erectile function and histopathological changes compared with the ADSCs group. CONCLUSIONS: IC-injected MTs resulted in a better restoration of erectile function than traditional single-cell strategy. The underlying mechanisms of recovery appear to involve enhanced cellular retention in the penis and upregulation of some paracrine factors.
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spelling pubmed-47087022016-01-26 AB182. Therapeutic potential of adipose-derived stem cells-based micro-tissues in a postprostatectomy erectile dysfunction rat model Guan, Ruili Xu, Yongde Lei, Hongen Gao, Zhezhu Xin, Zhongcheng Transl Androl Urol Moderated Poster Presentation OBJECTIVE: This study aims to investigate the feasibility and mechanism of adipose-derived stem cells (ADSCs)-based micro-tissues (MTs) in the treatment of ED in a rat model of bilateral cavernous nerves (CNs) injury. METHODS: ADSCs labeled with 5-ethynyl-2-deoxyuridine (EdU) were used to generate MTs with hanging drop method. Ten Sprague-Dawley (SD) rats underwent sham surgery and intracavernous (IC) injection of phosphate buffer solution (PBS) (the sham group). Another 70 rats underwent bilateral CN crush and were then treated with PBS (n=10, the crush group), dissociated ADSCs (n=30, the ADSCs group), and MTs (n=30, the MTs group), respectively. At day 1, 3, 7, 14 (n=5), and 28 (n=10) postsurgery, specimens were harvested for histology. At day 28, 10 rats in each group were examined for erectile function before tissue harvest. Light microscopy of the dynamic aggregation of the MT, immunohistologic examination of the MTs, the retention and distribution of EdU + ADSCs in the corpus cavernosum (CC), and the penis histological analyses of collagen content, Western blot of functional proteins in MTs, IC pressure recording on CN electrostimulation. RESULTS: Three-day-old MTs became stable and expressed nerve growth factor, vascular endothelial growth factor, C-X-C chemokine receptor type 4, Wnt5a, and collagen IV. More EdU + ADSCs retained in the CC in the MTs group than that in the ADSCs group. IC injection of MTs resulted in significant restoration of the erectile function and histopathological changes compared with the ADSCs group. CONCLUSIONS: IC-injected MTs resulted in a better restoration of erectile function than traditional single-cell strategy. The underlying mechanisms of recovery appear to involve enhanced cellular retention in the penis and upregulation of some paracrine factors. AME Publishing Company 2015-08 /pmc/articles/PMC4708702/ http://dx.doi.org/10.3978/j.issn.2223-4683.2015.s182 Text en 2015 Translational Andrology and Urology. All rights reserved.
spellingShingle Moderated Poster Presentation
Guan, Ruili
Xu, Yongde
Lei, Hongen
Gao, Zhezhu
Xin, Zhongcheng
AB182. Therapeutic potential of adipose-derived stem cells-based micro-tissues in a postprostatectomy erectile dysfunction rat model
title AB182. Therapeutic potential of adipose-derived stem cells-based micro-tissues in a postprostatectomy erectile dysfunction rat model
title_full AB182. Therapeutic potential of adipose-derived stem cells-based micro-tissues in a postprostatectomy erectile dysfunction rat model
title_fullStr AB182. Therapeutic potential of adipose-derived stem cells-based micro-tissues in a postprostatectomy erectile dysfunction rat model
title_full_unstemmed AB182. Therapeutic potential of adipose-derived stem cells-based micro-tissues in a postprostatectomy erectile dysfunction rat model
title_short AB182. Therapeutic potential of adipose-derived stem cells-based micro-tissues in a postprostatectomy erectile dysfunction rat model
title_sort ab182. therapeutic potential of adipose-derived stem cells-based micro-tissues in a postprostatectomy erectile dysfunction rat model
topic Moderated Poster Presentation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4708702/
http://dx.doi.org/10.3978/j.issn.2223-4683.2015.s182
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