posted on 2017-10-12, 00:00authored byDongdong Xiao, Hao Yan, Qiong Wang, Xiangguo Lv, Ming Zhang, Yang Zhao, Zhe Zhou, Jiping Xu, Qian Sun, Kang Sun, Wei Li, Mujun Lu
Bladder
acellular matrix graft-alginate dialdehyde-gelatin hydrogel-silk
mesh (BAMG-HS) encapsulated with adipose-derived stem cells (ASCs)
was evaluated in a rat model of augmentation cystoplasty, including
BAMG-HS-ASCs (n = 18, subgroup n = 6 for 2, 4, and 12 weeks), acellular
BAMG-HS (n = 6 for 12 weeks) and cystotomy control (n = 6 for 12 weeks)
groups. Equipped with good cytocompatibility and superior mechanical
properties (elastic modulus: 5.33 ± 0.96 MPa, maximum load: 28.90
± 0.69 N), BAMG-HS acted a trilayer “sandwich”
scaffold with minimal interference in systemic homeostasis. ASCs in
BAMG-HS promoted morphological and histological bladder restoration
by accelerating scaffold degradation (p < 0.05),
ameliorating fibrosis (p < 0.05) and inflammation
(p < 0.01). Additionally, ASCs facilitated the
recovery of bladder function by enhancing smooth muscle regeneration
(p < 0.05), innervation (p <
0.01) and angiogenesis (p < 0.001). Except for
a small number of endothelium-differentiated ASCs, the pro-angiogenic
effects of ASCs were mainly related to ERK1/2 phosphorylation in the
downstream of SDF-1α/CXCR4 pathway.