Suppr超能文献

用于最小化处理的自体膀胱组织扩张的电纺 PLGA、压缩胶原和切碎尿路上皮构建体。

Constructs of electrospun PLGA, compressed collagen and minced urothelium for minimally manipulated autologous bladder tissue expansion.

机构信息

Textile Department, Isfahan University of Technology, Isfahan, Iran; Division of Polymer Chemistry, A Science for Life Laboratory, Department of Chemistry - Ångström Laboratory, Uppsala University, Uppsala, Sweden.

Department of Women's and Children's Health, Centre of Molecular Medicine, Karolinska Institutet, Stockholm, Sweden; Department of Paediatric Surgery, Astrid Lindgren Children's Hospital, Karolinska University Hospital, Stockholm, Sweden.

出版信息

Biomaterials. 2014 Jul;35(22):5741-8. doi: 10.1016/j.biomaterials.2014.04.002. Epub 2014 Apr 24.

Abstract

Bladder regeneration based on minced bladder mucosa in vivo expansion is an alternative to in vitro culturing of urothelial cells. Here, we present the design of a hybrid, electrospun poly(lactic-co-glycolide) (PLGA) - plastically compressed (PC) collagen scaffold that could allow in vivo bladder mucosa expansion. Optimisation of electrospinning was performed in order to obtain increased pore sizes and porosity to consolidate the construct and to support neovascularisation and tissue ingrowth. Tensile tests showed an increase in average tensile strength from 0.6 MPa for PC collagen to 3.57 MPa for the hybrid construct. The optimised PLGA support scaffold was placed between two collagen gels, and the minced tissue was distributed either on top or both on top and inside the construct prior to PC; this was then cultured for up to four weeks. Morphology, histology and SEM demonstrated that the construct maintained its integrity throughout cell culture. Cells from minced tissue migrated, expanded and re-organised to a confluent cell layer on the top of the construct after two weeks and formed a multilayered urothelium after four weeks. Cell morphology and phenotype was typical for urothelial mucosa during tissue culture.

摘要

基于体内扩增的切碎膀胱黏膜的膀胱再生是体外培养尿路上皮细胞的替代方法。在这里,我们提出了一种混合的、电纺的聚(乳酸-共-乙醇酸)(PLGA)-塑性压缩(PC)胶原支架的设计,该支架可以允许体内膀胱黏膜的扩增。为了增加孔尺寸和孔隙率以巩固构建体并支持新血管生成和组织向内生长,对电纺进行了优化。拉伸试验表明,与 PC 胶原相比,混合结构的平均拉伸强度从 0.6 MPa 增加到 3.57 MPa。优化后的 PLGA 支撑支架被放置在两个胶原凝胶之间,切碎的组织被分布在构建体的顶部或顶部和内部,然后进行 PC;然后培养长达四周。形态学、组织学和 SEM 表明,该构建体在整个细胞培养过程中保持其完整性。两周后,来自切碎组织的细胞迁移、扩增并重新组织成构建体顶部的连续细胞层,四周后形成多层尿路上皮。组织培养过程中,细胞形态和表型是典型的尿路上皮黏膜。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验