Das Bodhisatwa, Seesala Sundeep V, Pal Pallabi, Roy Trina, Roy Preetam Guha, Dhara Santanu
Department of Biomedical Engineering, Indian Institute of Technology Ropar, Rupnagar, India.
School of Medical Science and Technology, Indian Institute of Technology Kharagpur, Kharagpur, India.
In Vitro Model. 2021 Oct 29;1(1):73-83. doi: 10.1007/s44164-021-00004-7. eCollection 2022 Feb.
Bone is the major connective tissue maintaining the structural integrity of the human body. However, fracture and many skeletal degenerative diseases can compromise this function. Thus, therapeutics related to bone degeneration are of significant research interest and require good in vitro models for such therapeutic evaluation. Bone is a highly vascularized tissue and incorporation of this feature is significantly important for mimicking the osteogenic microenvironment. In the current study, we developed a vascularized flat bone model via simultaneous mechanical actuation of mechanical strain and fluid shear. The mechanical strain was achieved by static magnetic field actuation of a magnetic nanocomposite scaffold. The fluid shear was generated by developing a micropattern on the magnetic nanocomposite via replica molding and laser-based microfabrication. From the live cell imaging window of the microdevice, both bone and vasculature like cellular morphology was observed. The SEM study showed thick ECM deposition in the dynamic culture. In the PCR study, both osteogenic (Col-1, osteocalcin) and angiogenic phenotypes (PECAM) were observed in the dynamic culture scaffolds while chondrogenic marker (Col-2) was downregulated.
The online version contains supplementary material available at 10.1007/s44164-021-00004-7.
骨骼是维持人体结构完整性的主要结缔组织。然而,骨折和许多骨骼退行性疾病会损害这一功能。因此,与骨退化相关的治疗方法具有重大研究意义,并且需要良好的体外模型进行此类治疗评估。骨骼是一种高度血管化的组织,纳入这一特征对于模拟成骨微环境至关重要。在本研究中,我们通过同时施加机械应变和流体剪切力的机械驱动,开发了一种血管化扁平骨模型。机械应变通过磁性纳米复合支架的静磁场驱动实现。流体剪切力通过复制成型和基于激光的微加工在磁性纳米复合材料上形成微图案产生。从微器件的活细胞成像窗口观察到了类似骨骼和脉管系统的细胞形态。扫描电子显微镜研究显示动态培养中有大量细胞外基质沉积。在聚合酶链反应研究中,动态培养支架中观察到了成骨(I型胶原、骨钙素)和血管生成表型(血小板内皮细胞黏附分子),而成软骨标记物(II型胶原)表达下调。
在线版本包含可在10.1007/s44164-021-00004-7获取的补充材料。