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基于在胶原蛋白基质中控制释放成纤维细胞生长因子-2的脂肪组织工程。

Adipose tissue engineering based on the controlled release of fibroblast growth factor-2 in a collagen matrix.

作者信息

Vashi Aditya V, Abberton Keren M, Thomas Gregory P, Morrison Wayne A, O'Connor Andrea J, Cooper-White Justin J, Thompson Erik W

机构信息

Bernard O'Brien Institute of Microsurgery, St. Vincent's Hospital, Fitzroy, Victoria, Australia.

出版信息

Tissue Eng. 2006 Nov;12(11):3035-43. doi: 10.1089/ten.2006.12.3035.

Abstract

Adipose tissue forms when basement membrane extract (Matrigel) and fibroblast growth factor-2 (FGF-2) are added to our mouse tissue engineering chamber model. A mouse tumor extract, Matrigel is unsuitable for human clinical application, and finding an alternative to Matrigel is essential. In this study we generated adipose tissue in the chamber model without using Matrigel by controlled release of FGF-2 in a type I collagen matrix. FGF-2 was impregnated into biodegradable gelatin microspheres for its slow release. The chambers were filled with these microspheres suspended in 60 microL collagen gel. Injection of collagen containing free FGF-2 or collagen containing gelatin microspheres with buffer alone served as controls. When chambers were harvested 6 weeks after implantation, the volume and weight of the tissue obtained were higher in the group that received collagen and FGF-2 impregnated microspheres than in controls. Histologic analysis of tissue constructs showed the formation of de novo adipose tissue accompanied by angiogenesis. In contrast, control groups did not show extensive adipose tissue formation. In conclusion, this study has shown that de novo formation of adipose tissue can be achieved through controlled release of FGF-2 in collagen type I in the absence of Matrigel.

摘要

当将基底膜提取物(基质胶)和成纤维细胞生长因子-2(FGF-2)添加到我们的小鼠组织工程腔室模型中时,脂肪组织会形成。基质胶作为一种小鼠肿瘤提取物,不适用于人类临床应用,因此寻找基质胶的替代品至关重要。在本研究中,我们通过在I型胶原基质中控制释放FGF-2,在不使用基质胶的腔室模型中生成了脂肪组织。FGF-2被包埋在可生物降解的明胶微球中以实现其缓慢释放。腔室中填充有悬浮在60微升胶原凝胶中的这些微球。注射含有游离FGF-2的胶原或仅含有缓冲液的明胶微球的胶原作为对照。植入6周后取出腔室时,接受胶原和FGF-2包埋微球的组中获得的组织体积和重量高于对照组。组织构建体的组织学分析显示,伴随血管生成形成了新生脂肪组织。相比之下,对照组未显示出广泛的脂肪组织形成。总之,本研究表明,在没有基质胶的情况下,通过在I型胶原中控制释放FGF-2可以实现脂肪组织的新生。

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