Xie Jing, Peng Chen, Zhao Qinghua, Wang Xianliu, Yuan Huihua, Yang Liangliang, Li Kai, Lou Xiangxin, Zhang Yanzhong
College of Chemistry, Chemical Engineering & Biotechnology, Donghua University, Shanghai 201620, China; Key Laboratory of Eco-Textile, Ministry of Education, Donghua University, Shanghai 201620, China.
Department of Radiology, Shanghai Tenth People's Hospital, Tongji University, Shanghai 200072, China.
Acta Biomater. 2016 Jan;29:365-379. doi: 10.1016/j.actbio.2015.10.007. Epub 2015 Oct 9.
Induced pluripotent stem cell-derived mesenchymal stem cells (iPSC-MSCs) are a new type of MSCs that come with attractive merits over the iPSCs per se. Aimed for regenerating bone tissues, this study was designed to investigate osteogenic differentiation and bone regeneration capacities of iPSC-MSCs by using biomimetic nanofibers of hydroxyapatite/collagen/chitosan (HAp/Col/CTS). Murine iPSCs were firstly induced to differentiate into iPSC-MSCs and thoroughly characterized. Effects of HAp/Col/CTS nanofibers prepared from electrospinning of Col-doped HAp/CTS nanocomposite, on osteogenic differentiation of the generated iPSC-MSCs were then evaluated in detail, including cell morphology, proliferation, migration, quantified specific osteogenic gene and protein expressions. Compared with different controls (TCP, CTS, and HAp/CTS), the HAp/Col/CTS scaffold was found to have more favorable effects on attachment and proliferation of iPSC-MSCs than others (P<0.01). Expressions of osteogenic genes, Runx2, Ocn, Alp, and Col, were significantly upregulated in iPSC-MSCs cultured on HAp/Col/CTS than CTS (P<0.01). Similarly, there appeared considerably higher secreting activities of osteogenesis protein markers, ALP and Col. Furthermore, mouse cranial defects were created to investigate efficacy of using iPSC-MSCs in combination with HAp/Col/CTS scaffold for regenerative bone repair in vivo. Examinations by computed tomography (CT) imaging, bone mineral density and hematoxylin eosin (HE) staining corroborated that cell-scaffold construct of iPSC-MSCs+HAp/Col/CTS could effectively promote bone regeneration. After 6 weeks of implantation, bone mineral density of the iPSC-MSCs+HAp/Col/CTS group was found to be nearly 2-fold higher than others. Our results demonstrated that biomimetic nanofibers of HAp/Col/CTS promoted the osteogenic differentiation and bone regeneration of iPSC-MSCs. The iPSC-MSCs+HAp/Col/CTS complex could be used as a new 'stem cell-scaffold' system for realizing personalized and efficacious bone regeneration in future.
In bone tissue engineering, stem cells have become the most important source of seed cells. iPSC-MSCs are a new type of MSCs that come with attractive merits over the iPSCs per se. However, how to obtain befitting iPSC-MSCs and regulate their osteogenic differentiation are the key issues to be addressed. Given the great biomimicking capacity to extracellular matrix, electrospun nanofibers may be explored to modulate osteogenic differentiation of the iPSC-MSCs. This study successfully demonstrated that biomimetic nanofibers of HAp/Col/CTS significantly promoted the osteogenic differentiation and bone regeneration of iPSC-MSCs, which thereby suggests that nanofibrous scaffold supported iPSC-MSCs complex may be a new 'stem cell-scaffold' system for regulating the fate of osteogenic differentiation of iPSC-MSCs towards patient-specific bone regeneration in future.
诱导多能干细胞衍生的间充质干细胞(iPSC-MSCs)是一种新型的间充质干细胞,相对于诱导多能干细胞本身具有吸引人的优点。本研究旨在利用羟基磷灰石/胶原蛋白/壳聚糖(HAp/Col/CTS)的仿生纳米纤维再生骨组织,研究iPSC-MSCs的成骨分化和骨再生能力。首先将小鼠诱导多能干细胞诱导分化为iPSC-MSCs并进行全面表征。然后详细评估由掺杂Col的HAp/CTS纳米复合材料静电纺丝制备的HAp/Col/CTS纳米纤维对所生成的iPSC-MSCs成骨分化的影响,包括细胞形态、增殖、迁移、定量特定成骨基因和蛋白表达。与不同对照组(TCP、CTS和HAp/CTS)相比,发现HAp/Col/CTS支架对iPSC-MSCs的附着和增殖具有比其他组更有利的影响(P<0.01)。在HAp/Col/CTS上培养的iPSC-MSCs中成骨基因Runx2、Ocn、Alp和Col的表达比CTS组显著上调(P<0.01)。同样,成骨蛋白标志物ALP和Col的分泌活性也明显更高。此外,制造小鼠颅骨缺损以研究iPSC-MSCs与HAp/Col/CTS支架联合用于体内再生骨修复的效果。计算机断层扫描(CT)成像、骨矿物质密度和苏木精伊红(HE)染色检查证实,iPSC-MSCs+HAp/Col/CTS的细胞-支架构建体可有效促进骨再生。植入6周后,发现iPSC-MSCs+HAp/Col/CTS组的骨矿物质密度比其他组高近2倍。我们的结果表明,HAp/Col/CTS的仿生纳米纤维促进了iPSC-MSCs的成骨分化和骨再生。iPSC-MSCs+HAp/Col/CTS复合物可作为一种新的“干细胞-支架”系统,用于未来实现个性化和有效的骨再生。
在骨组织工程中,干细胞已成为最重要的种子细胞来源。iPSC-MSCs是一种新型的间充质干细胞,相对于诱导多能干细胞本身具有吸引人的优点。然而,如何获得合适的iPSC-MSCs并调节其成骨分化是需要解决的关键问题。鉴于对细胞外基质具有强大的仿生能力,可探索静电纺纳米纤维来调节iPSC-MSCs的成骨分化。本研究成功证明,HAp/Col/CTS的仿生纳米纤维显著促进了iPSC-MSCs的成骨分化和骨再生,这表明纳米纤维支架支持的iPSC-MSCs复合物可能是一种新的“干细胞-支架”系统,用于未来调节iPSC-MSCs的成骨分化命运以实现患者特异性骨再生。