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通过依赖于形貌的谱系特异性分化诱导,用于体内多种组织再生的电纺支架。

Electrospun scaffolds for multiple tissues regeneration in vivo through topography dependent induction of lineage specific differentiation.

机构信息

Department of Sports Medicine, School of Medicine, Zhejiang University, Hangzhou, China; Zhejiang Provincial Key Laboratory of Tissue Engineering and Regenerative Medicine, Hangzhou, China.

Department of Rehabilitation, Sir Run Run Shaw Hospital, School of Medicine, Zhejiang University, Hangzhou, China.

出版信息

Biomaterials. 2015 Mar;44:173-85. doi: 10.1016/j.biomaterials.2014.12.027. Epub 2015 Jan 12.

Abstract

Physical topographic cues from various substrata have been shown to exert profound effects on the growth and differentiation of stem cells due to their niche-mimicking features. However, the biological function of different topographic materials utilized as bio-scaffolds in vivo have not been rigorously characterized. This study investigated the divergent differentiation pathways of mesenchymal stem cells (MSCs) and neo-tissue formation trigged by aligned and randomly-oriented fibrous scaffolds, both in vitro and in vivo. The aligned group was observed to form more mature tendon-like tissue in the Achilles tendon injury model, as evidenced by histological scoring and collagen I immunohistochemical staining data. In contrast, the randomly-oriented group exhibited much chondrogenesis and subsequent bone tissue formation through ossification. Additionally, X-ray imaging and osteocalcin immunohistochemical staining also demonstrated that osteogenesis in vivo is driven by randomly oriented topography. Furthermore, MSCs on the aligned substrate exhibited tenocyte-like morphology and enhanced tenogenic differentiation compared to cells grown on randomly-oriented scaffold. qRT-PCR analysis of osteogenic marker genes and alkaline phosphatase (ALP) staining demonstrated that MSCs cultured on randomly-oriented fiber scaffolds displayed enhanced osteogenic differentiation compared with cells cultured on aligned fiber scaffolds. Finally, it was demonstrated that cytoskeletal tension release abrogated the divergent differentiation pathways on different substrate topography. Collectively, these findings illustrate the relationship between topographic cues of the scaffold and their inductive role in tissue regeneration; thus providing an insight into future development of smart functionalized bio-scaffold design and its application in tissue engineering.

摘要

由于具有类似微环境的特点,各种基底的物理拓扑线索已被证明对干细胞的生长和分化有深远影响。然而,作为体内生物支架使用的不同拓扑材料的生物功能尚未得到严格的表征。本研究通过体外和体内实验,研究了定向和随机取向纤维支架对间充质干细胞(MSCs)的不同分化途径和新组织形成的影响。在跟腱损伤模型中,定向组形成了更成熟的肌腱样组织,组织学评分和 I 型胶原免疫组化染色数据证实了这一点。相比之下,随机组则通过成骨作用表现出更多的软骨生成和随后的骨组织形成。此外,X 射线成像和骨钙素免疫组化染色也表明,体内成骨是由随机取向的拓扑结构驱动的。此外,与在随机取向支架上生长的细胞相比,在定向基底上的 MSCs 表现出肌腱细胞样形态和增强的肌腱分化。对成骨标志物基因的 qRT-PCR 分析和碱性磷酸酶(ALP)染色表明,与在定向纤维支架上培养的细胞相比,在随机纤维支架上培养的 MSCs 表现出增强的成骨分化。最后,证明细胞骨架张力释放消除了不同基底拓扑结构上的不同分化途径。总之,这些发现说明了支架的拓扑线索与其在组织再生中的诱导作用之间的关系;为智能功能化生物支架设计及其在组织工程中的应用提供了新的见解。

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