Department of Biomedical Engineering, Chang Gung University, Taoyuan 33302, Taiwan.
Department of Orthopedic Surgery, Chang Gung Memorial Hospital, Linkou 33305, Taiwan.
ACS Appl Mater Interfaces. 2023 Oct 25;15(42):49051-49059. doi: 10.1021/acsami.3c12925. Epub 2023 Oct 17.
Periosteum-derived progenitor cells (PDPCs) are highly promising cell sources that are indispensable in the bone healing process. Adipose-derived stem cells (ADSCs) are physiologically close to periosteum tissue and release multiple growth factors to promote the bone healing process. Co-culturing PDPCs and ADSCs can construct periosteum-bone tissue microenvironments for the study of cellular crosstalk and molecular signal in the bone healing process. In the current work, a paper-based osteogenesis-on-a-chip platform was successfully developed to provide an in vitro three-dimensional coculture model. The platform was a paper substrate sandwiched between PDPC-hydrogel and ADSC-hydrogel suspensions. Cell secretion could be transferred through the paper substrate from one side to another side. Growth factors including BMP2, TGF-β, POSTN, Wnt proteins, PDGFA, and VEGFA were directly analyzed by a paper-based immunoassay. Cellular crosstalk was studied by protein expression on the paper substrate. Moreover, osteogenesis of PDPCs was investigated by examining the mRNA expressions of PDPCs after culture. Neutralizing and competitive assays were conducted to understand the correlation between growth factors secreted from ADSCs and the osteogenesis of PDPCs. In vitro periosteum-bone tissue microenvironment was established by the paper-based osteogenesis-on-a-chip platform. The proposed approach provides a promising assay of cellular crosstalk and molecular signal in 3D coculture microenvironment that may potentially lead to the development of effective bone regeneration therapy.
骨膜来源祖细胞(PDPCs)是极具潜力的细胞来源,在骨愈合过程中不可或缺。脂肪来源干细胞(ADSCs)在生理上与骨膜组织接近,并释放多种生长因子来促进骨愈合过程。共培养 PDPCs 和 ADSCs 可以构建骨膜-骨组织微环境,用于研究骨愈合过程中的细胞串扰和分子信号。在当前工作中,成功开发了基于纸的成骨芯片平台,提供了体外三维共培养模型。该平台是由 PDPC-水凝胶和 ADSC-水凝胶悬浮液夹在中间的纸基。细胞分泌可以通过纸基从一侧转移到另一侧。通过纸基免疫分析直接分析 BMP2、TGF-β、POSTN、Wnt 蛋白、PDGFA 和 VEGFA 等生长因子。通过在纸基上检测蛋白表达研究细胞串扰。此外,通过培养后检测 PDPCs 的 mRNA 表达来研究 PDPCs 的成骨作用。进行中和和竞争测定以了解 ADSCs 分泌的生长因子与 PDPCs 成骨之间的相关性。基于纸的成骨芯片平台建立了体外骨膜-骨组织微环境。该方法提供了一种在 3D 共培养微环境中研究细胞串扰和分子信号的有前途的方法,可能为有效的骨再生治疗方法的开发提供了依据。