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多层致密胶原-丝素蛋白复合物:间充质干细胞向软骨生成和成骨谱系分化的平台

Multilayered dense collagen-silk fibroin hybrid: a platform for mesenchymal stem cell differentiation towards chondrogenic and osteogenic lineages.

作者信息

Ghezzi Chiara E, Marelli Benedetto, Donelli Ilaria, Alessandrino Antonio, Freddi Giuliano, Nazhat Showan N

机构信息

Department of Mining and Materials Engineering, McGill University, Montreal, Quebec, Canada.

Innovhub-Stazioni Sperimentali per l'Industria, Div. Stazione Sperimentale per la Seta, Milan, Italy.

出版信息

J Tissue Eng Regen Med. 2017 Jul;11(7):2046-2059. doi: 10.1002/term.2100. Epub 2015 Nov 9.

DOI:10.1002/term.2100
PMID:26549403
Abstract

Type I collagen is a major structural and functional protein in connective tissues. However, collagen gels exhibit unstable geometrical properties, arising from extensive cell-mediated contraction. In an effort to stabilize collagen-based hydrogels, plastic compression was used to hybridize dense collagen (DC) with electrospun silk fibroin (SF) mats, generating multilayered DC-SF-DC constructs. Seeded mesenchymal stem cell (MSC)-mediated DC-SF-DC contraction, as well as growth and differentiation under chondrogenic and osteogenic supplements, were compared to those seeded in DC and on SF alone. The incorporation of SF within DC prevented extensive cell-mediated collagen gel contraction. The effect of the multilayered hybrid on MSC remodelling capacity was also evident at the transcription level, where the expression of matrix metalloproteinases and their inhibitor (MMP1, MMP2, MMP3, MMP13 and Timp1) by MSCs within DC-SF-DC were comparable to those on SF and significantly downregulated in comparison to DC, except for Timp1. Chondrogenic supplements stimulated extracellular matrix production within the construct, stabilizing its multilayered structure and promoting MSC chondrogenic differentiation, as indicated by the upregulation of the genes Col2a1 and Agg and the production of collagen type II. In osteogenic medium there was an upregulation in ALP and OP along with the presence of an apatitic phase, indicating MSC osteoblastic differentiation and matrix mineralization. In sum, these results have implications on the modulation of three-dimensional collagen-based gel structural stability and on the stimulation and maintenance of the MSC committed phenotype inherent to the in vitro formation of chondral tissue and bone, as well as on potential multilayered complex tissues. Copyright © 2015 John Wiley & Sons, Ltd.

摘要

I型胶原蛋白是结缔组织中的一种主要结构和功能蛋白。然而,胶原蛋白凝胶呈现出不稳定的几何特性,这是由广泛的细胞介导收缩引起的。为了稳定基于胶原蛋白的水凝胶,采用塑性压缩法将致密胶原蛋白(DC)与电纺丝素蛋白(SF)垫杂交,生成多层DC-SF-DC构建体。将接种间充质干细胞(MSC)介导的DC-SF-DC收缩以及在软骨生成和成骨补充剂下的生长和分化,与单独接种在DC和SF上的情况进行比较。在DC中加入SF可防止广泛的细胞介导的胶原蛋白凝胶收缩。多层杂交体对MSC重塑能力的影响在转录水平也很明显,DC-SF-DC内的MSC表达基质金属蛋白酶及其抑制剂(MMP1、MMP2、MMP3、MMP13和Timp1)与SF上的情况相当,与DC相比,除Timp1外均显著下调。软骨生成补充剂刺激构建体内细胞外基质的产生,稳定其多层结构并促进MSC软骨生成分化,这通过基因Col2a1和Agg的上调以及II型胶原蛋白的产生得以体现。在成骨培养基中,碱性磷酸酶(ALP)和骨桥蛋白(OP)上调,同时存在磷灰石相,表明MSC向成骨细胞分化和基质矿化。总之,这些结果对基于三维胶原蛋白的凝胶结构稳定性的调节、对软骨组织和骨体外形成所固有的MSC定向表型的刺激和维持以及对潜在的多层复杂组织都有意义。版权所有© 2015约翰威立父子有限公司。

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