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采用自行设计的灌注系统制备的膀胱脱细胞基质与脂肪来源干细胞促进膀胱组织再生

Bladder Acellular Matrix Prepared by a Self-Designed Perfusion System and Adipose-Derived Stem Cells to Promote Bladder Tissue Regeneration.

作者信息

Xiao Shuwei, Wang Pengchao, Zhao Jian, Ling Zhengyun, An Ziyan, Fu Zhouyang, Fu Weijun, Zhou Jin, Zhang Xu

机构信息

Department of Urology, The Third Medical Centre, Chinese PLA General Hospital, Beijing, China.

Medical School of Chinese PLA, Beijing, China.

出版信息

Front Bioeng Biotechnol. 2022 Jun 22;10:794603. doi: 10.3389/fbioe.2022.794603. eCollection 2022.

Abstract

The bladder patch constructed with the bladder acellular matrix (BAM) and adipose-derived stem cells (ASCs) was incubated with the omentum for bladder reconstruction in a rat model of bladder augmentation cystoplasty. A self-designed perfusion system and five different decellularization protocols were used to prepare the BAM. Finally, an optimal protocol (group C) was screened out by comparing the cell nucleus residue, collagen structure preservation and biologically active components retention of the prepared BAM. ASCs-seeded (BAM-ASCs group) and unseeded BAM (BAM group) were incubated with the omentum for 7 days to promote neovascularization and then perform bladder reconstruction. Hematoxylin and eosin and Masson's trichrome staining indicated that the bladder patches in the BAM-ASCs group could better regenerate the bladder wall structure compared to the BAM group. Moreover, immunofluorescence analyses demonstrated that the ASCs could promote the regeneration of smooth muscle, neurons and blood vessels, and the physiological function (maximal bladder capacity, max pressure prior to voiding and bladder compliance) restoration in the BAM-ASCs group. The results demonstrated that the self-designed perfusion system could quickly and efficiently prepare the whole bladder scaffold and confirmed that the prepared BAM could be used as the scaffold material for functional bladder tissue engineering applications.

摘要

在膀胱扩大膀胱成形术大鼠模型中,将由膀胱脱细胞基质(BAM)和脂肪来源干细胞(ASCs)构建的膀胱补片与大网膜一起孵育以进行膀胱重建。使用自行设计的灌注系统和五种不同的脱细胞方案来制备BAM。最后,通过比较所制备BAM的细胞核残留、胶原结构保留和生物活性成分保留情况,筛选出最佳方案(C组)。将接种有ASCs的BAM(BAM-ASCs组)和未接种ASCs的BAM(BAM组)与大网膜一起孵育7天以促进新血管形成,然后进行膀胱重建。苏木精-伊红染色和Masson三色染色表明,与BAM组相比,BAM-ASCs组的膀胱补片能够更好地再生膀胱壁结构。此外,免疫荧光分析表明,ASCs可促进平滑肌、神经元和血管的再生,以及BAM-ASCs组的生理功能(最大膀胱容量、排尿前最大压力和膀胱顺应性)恢复。结果表明,自行设计的灌注系统能够快速有效地制备全膀胱支架,并证实所制备的BAM可作为功能性膀胱组织工程应用的支架材料。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/22f1/9257038/853d0cccfef5/fbioe-10-794603-g007.jpg

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