Suppr超能文献

人脐带华通氏胶干细胞与人类关节软骨细胞共培养的体外软骨形成定向分化

In vitro chondrogenic commitment of human Wharton's jelly stem cells by co-culture with human articular chondrocytes.

作者信息

Pereira R C, Costa-Pinto A R, Frias A M, Neves N M, Azevedo H S, Reis R L

机构信息

3Bs Research Group - Biomaterials, Biodegradables and Biomimetics, University of Minho, Headquarters of the European Institute of Excellence on Tissue Engineering and Regenerative Medicine, AvePark, Guimarães, Portugal.

ICVS/3Bs PT Government-associated Laboratory, Braga/Guimarães, Portugal.

出版信息

J Tissue Eng Regen Med. 2017 Jun;11(6):1876-1887. doi: 10.1002/term.2085. Epub 2015 Sep 7.

Abstract

Wharton's jelly stem cells (WJSCs) are a potential source of transplantable stem cells in cartilage-regenerative strategies, due to their highly proliferative and multilineage differentiation capacity. We hypothesized that a non-direct co-culture system with human articular chondrocytes (hACs) could enhance the potential chondrogenic phenotype of hWJSCs during the expansion phase compared to those expanded in monoculture conditions. Primary hWJSCs were cultured in the bottom of a multiwell plate separated by a porous transwell membrane insert seeded with hACs. No statistically significant differences in hWJSCs duplication number were observed under either of the culture conditions during the expansion phase. hWJSCs under co-culture conditions show upregulations of collagen type I and II, COMP, TGFβ1 and aggrecan, as well as of the main cartilage transcription factor, SOX9, when compared to those cultured in the absence of chondrocytes. Chondrogenic differentiation of hWJSCs, previously expanded in co-culture and monoculture conditions, was evaluated for each cellular passage using the micromass culture model. Cells expanded in co-culture showed higher accumulation of glycosaminoglycans (GAGs) compared to cells in monoculture, and immunohistochemistry for localization of collagen type I revealed a strong detection signal when hWJSCs were expanded under monoculture conditions. In contrast, type II collagen was detected when cells were expanded under co-culture conditions, where numerous round-shaped cell clusters were observed. Using a micromass differentiation model, hWJSCs, previously exposed to soluble factors secreted by hACs, were able to express higher levels of chondrogenic genes with deposition of cartilage extracellular matrix components, suggesting their use as an alternative cell source for treating degenerated cartilage. Copyright © 2015 John Wiley & Sons, Ltd.

摘要

华通胶干细胞(WJSCs)因其高度增殖和多向分化能力,成为软骨再生策略中可移植干细胞的潜在来源。我们推测,与在单培养条件下扩增的细胞相比,在扩张期使用与人关节软骨细胞(hACs)的非直接共培养系统可以增强hWJSCs的潜在软骨形成表型。原代hWJSCs培养于多孔板底部,与接种了hACs的多孔Transwell膜插入物隔开。在扩张期,两种培养条件下hWJSCs的复制数均未观察到统计学显著差异。与在无软骨细胞条件下培养的细胞相比,共培养条件下的hWJSCs显示出I型和II型胶原蛋白、软骨寡聚基质蛋白(COMP)、转化生长因子β1(TGFβ1)、聚集蛋白聚糖以及主要软骨转录因子SOX9的上调。对于先前在共培养和单培养条件下扩增的hWJSCs的每个细胞传代,使用微团培养模型评估其软骨分化情况。与单培养的细胞相比,共培养扩增的细胞显示出更高的糖胺聚糖(GAGs)积累,并且当hWJSCs在单培养条件下扩增时,I型胶原蛋白定位的免疫组织化学显示出强烈的检测信号。相反,当细胞在共培养条件下扩增时检测到II型胶原蛋白,此时观察到许多圆形细胞簇。使用微团分化模型,先前暴露于hACs分泌的可溶性因子的hWJSCs能够表达更高水平的软骨形成基因,并沉积软骨细胞外基质成分,这表明它们可作为治疗退化软骨的替代细胞来源。版权所有© 2015约翰威立父子有限公司。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验