2015
DOI: 10.1177/1535370215600101
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Tissue-engineered tubular substitutions for urinary diversion in a rabbit model

Abstract: Clinically, autologous gastrointestinal segments are traditionally used for urinary diversion. However, this procedure often causes many serious complications. Tissue engineering may provide an alternative treatment method in urinary diversion. This research aims to produce tissue-engineered tubular substitutions by using homologous adipose-derived stem cells, smooth muscle cells, and bladder acellular matrix in developing urinary diversion in a rabbit model. Adipose-derived stem cells and smooth muscle cells … Show more

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Cited by 12 publications
(5 citation statements)
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“…Jejunum [ 81 ] [ 80 ] [ 79 ] [ 78 ] [ 77 ] scaffold is more potent promoting cell proliferation and angiogenesis compared to scaffolds of bladder [ 81 ]. However, visceral scaffolds may not be, or less, effective for parenchymal organs regeneration [ 82 ].…”
Section: Visceral Organsmentioning
confidence: 99%
“…Jejunum [ 81 ] [ 80 ] [ 79 ] [ 78 ] [ 77 ] scaffold is more potent promoting cell proliferation and angiogenesis compared to scaffolds of bladder [ 81 ]. However, visceral scaffolds may not be, or less, effective for parenchymal organs regeneration [ 82 ].…”
Section: Visceral Organsmentioning
confidence: 99%
“…Due to significant problems associated with the use of gastrointestinal segments for bladder augmentation, new methods for urinary tract reconstruction are being sought 9 , 10 . Most of these methods use cell-seeded matrices to build tissue-engineered tubular grafts 11 , 12 . New, biologically derived scaffolds seeded with autologous cells for bladder wall substitution are also investigated 13 15 .…”
Section: Introductionmentioning
confidence: 99%
“…In the product, bovine type-I collagen was used to support live fibroblasts for the purpose of facilitating the healing process [ 7 ]. Recently, special acellular materials have been used in the same process; they contain growth factors derived from the urinary bladder and placental bed [ 8 , 9 , 10 ]. They constitute a non-toxic in vitro environment and promote adhesion, infiltration and proliferation of human fibroblasts and keratinocites.…”
Section: Introductionmentioning
confidence: 99%