4.8 Article

Bioinspired Silk Fibroin Mineralization for Advanced In Vitro Bone Remodeling Models

期刊

ADVANCED FUNCTIONAL MATERIALS
卷 32, 期 41, 页码 -

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/adfm.202206992

关键词

biomineralizations; bone remodeling; in vitro models; poly-aspartic acid; silk fibroins

资金

  1. research program TTW - Netherlands Organization for Scientific Research (NWO) [TTW 016.Vidi.188.021]
  2. European Research Council (ERC) [H2020-ERC-2017-ADV-788982-COLMIN]
  3. NWO [VI.Veni.192.094]

向作者/读者索取更多资源

In this study, a bone-mimetic template was developed using silk fibroin, poly-aspartic acid, and simulated body fluid. This model showed support for osteoclastic resorption and osteoblastic mineralization, mimicking the physiological bone remodeling process. The study highlights the potential importance of investigating cell-matrix interactions and using in vitro models for drug testing in bone remodeling pathologies like osteoporosis.
Human in vitro bone models can create the possibility for investigation of physiological bone remodeling while addressing the principle of replacement, reduction and refinement of animal experiments (3R). Current in vitro models lack cell-matrix interactions and their spatiotemporal complexity. To facilitate these analyses, a bone-mimetic template is developed in this study, inspired by bone's extracellular matrix composition and organization. Silk fibroin (SF) is used as an organic matrix, poly-aspartic acid (pAsp) is used to mimic the functionality of noncollagenous proteins, and 10x simulated body fluid serves as mineralization solution. By using pAsp in the mineralization solution, minerals are guided toward the SF material resulting in mineralization inside and as a coating on top of the SF. After cytocompatibility testing, remodeling experiments are performed in which mineralized scaffold remodeling by osteoclasts and osteoblasts is tracked with nondestructive microcomputed tomography and medium analyses over a period of 42 d. The mineralized scaffolds support osteoclastic resorption and osteoblastic mineralization, in the physiological bone remodeling specific sequence. This model could therefore facilitate the investigation of cell-matrix interactions and may thus reduce animal experiments and advance in vitro drug testing for bone remodeling pathologies like osteoporosis, where cell-matrix interactions need to be targeted.

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