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基于等距微柱阵列的仿生纤维通过力学适应性决定软骨细胞命运。

Biomimetic Fibers Based on Equidistant Micropillar Arrays Determines Chondrocyte Fate via Mechanoadaptability.

机构信息

State Key Laboratory of Oral Diseases, West China Hospital of Stomatology, Sichuan University, Chengdu, 610064, China.

National Clinical Research Center for Oral Diseases, West China Hospital of Stomatology, Sichuan University, Chengdu, 610064, China.

出版信息

Adv Healthc Mater. 2023 Dec;12(30):e2301685. doi: 10.1002/adhm.202301685. Epub 2023 Aug 24.

Abstract

It is recognized that the changes in the physical properties of extracellular matrix (ECM) result in fine-tuned cell responses including cell morphology, proliferation and differentiation. In this study, a novel patterned equidistant micropillar substrate based on polydimethylsiloxane (PDMS) is designed to mimic the collagen fiber-like network of the cartilage matrix. By changing the component of the curing agent to an oligomeric base, micropillar substrates with the same topology but different stiffnesses are obtained and it is found that chondrocytes seeded onto the soft micropillar substrate maintain their phenotype by gathering type II collagen and aggrecan more effectively than those seeded onto the stiff micropillar substrate. Moreover, chondrocytes sense and respond to micropillar substrates with different stiffnesses by altering the ECM-cytoskeleton-focal adhesion axis. Further, it is found that the soft substrate-preserved chondrocyte phenotype is dependent on the activation of Wnt/β-catenin signaling. Finally, it is indicated that the changes in osteoid-like region formation and cartilage phenotype loss in the stiffened sclerotic area of osteoarthritis cartilage to validate the changes triggered by micropillar substrates with different stiffnesses. This study provides the cell behavior changes that are more similar to those of real chondrocytes at tissue level during the transition from a normal state to a state of osteoarthritis.

摘要

人们认识到细胞外基质(ECM)的物理性质的变化会导致细胞精细的反应,包括细胞形态、增殖和分化。在这项研究中,设计了一种基于聚二甲基硅氧烷(PDMS)的新型等距微柱图案化基底,以模拟软骨基质中的胶原纤维样网络。通过改变固化剂的成分成为低聚物碱,获得了具有相同拓扑结构但不同硬度的微柱基底,并且发现接种在软微柱基底上的软骨细胞通过更有效地聚集 II 型胶原和聚集蛋白聚糖来保持其表型,而接种在硬微柱基底上的软骨细胞则不然。此外,软骨细胞通过改变细胞外基质-细胞骨架-黏附斑轴来感知和响应具有不同硬度的微柱基底。此外,还发现软基底保留的软骨细胞表型依赖于 Wnt/β-连环蛋白信号的激活。最后,通过改变刚度不同的微柱基底来验证骨关节炎软骨硬化区中类骨质样区域形成和软骨表型丢失的变化,从而验证了刚度不同的微柱基底所引发的变化。本研究提供了细胞行为的变化,这些变化在从正常状态到骨关节炎状态的转变过程中,更类似于组织水平上的真实软骨细胞的变化。

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