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载脂肪间充质干细胞的三层三维水凝胶复合支架通过 SDF-1α/CXCR4 通路促进膀胱重建。

Trilayer Three-Dimensional Hydrogel Composite Scaffold Containing Encapsulated Adipose-Derived Stem Cells Promotes Bladder Reconstruction via SDF-1α/CXCR4 Pathway.

机构信息

Department of Urology and Andrology, Ren Ji Hospital, School of Medicine, Shanghai Jiao Tong University , Shanghai 200001, China.

Department of Urology, The Sun Yat-sen Memorial Hospital, Sun Yat-sen University , Guangzhou 510120, China.

出版信息

ACS Appl Mater Interfaces. 2017 Nov 8;9(44):38230-38241. doi: 10.1021/acsami.7b10630. Epub 2017 Oct 27.

DOI:10.1021/acsami.7b10630
PMID:29022693
Abstract

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.

摘要

膀胱去细胞基质移植物-藻酸钠二醛-明胶水凝胶-丝素网(BAMG-HS)包裹脂肪来源干细胞(ASCs),在大鼠增强性膀胱扩大术模型中进行了评估,包括 BAMG-HS-ASCs(n = 18,亚组 n = 6,用于 2、4 和 12 周)、去细胞 BAMG-HS(n = 6,用于 12 周)和膀胱切开术对照组(n = 6,用于 12 周)。BAMG-HS 具有良好的细胞相容性和卓越的机械性能(弹性模量:5.33 ± 0.96 MPa,最大载荷:28.90 ± 0.69 N),充当具有最小系统内环境干扰的三层“三明治”支架。BAMG-HS 中的 ASC 通过加速支架降解(p < 0.05)、改善纤维化(p < 0.05)和炎症(p < 0.01),促进形态和组织学膀胱恢复。此外,通过增强平滑肌再生(p < 0.05)、神经支配(p < 0.01)和血管生成(p < 0.001),ASC 促进了膀胱功能的恢复。除了少数分化为内皮细胞的 ASC 外,ASC 的促血管生成作用主要与 SDF-1α/CXCR4 通路下游的 ERK1/2 磷酸化有关。

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