Sharaf Ahmed, Roos Brian, Timmerman Raissa, Kremers Gert-Jan, Bajramovic Jeffrey John, Accardo Angelo
Department of Precision and Microsystems Engineering, Delft University of Technology, Delft, Netherlands.
Alternatives Unit, Biomedical Primate Research Centre, Rijswijk, Netherlands.
Front Bioeng Biotechnol. 2022 Jul 22;10:926642. doi: 10.3389/fbioe.2022.926642. eCollection 2022.
Microglia are the resident macrophages of the central nervous system and contribute to maintaining brain's homeostasis. Current 2D "petri-dish" cell culturing platforms employed for microglia, are unrepresentative of the softness or topography of native brain tissue. This often contributes to changes in microglial morphology, exhibiting an amoeboid phenotype that considerably differs from the homeostatic ramified phenotype in healthy brain tissue. To overcome this problem, multi-scale engineered polymeric microenvironments are developed and tested for the first time with primary microglia derived from adult rhesus macaques. In particular, biomimetic 2.5D micro- and nano-pillar arrays (diameters = 0.29-1.06 µm), featuring low effective shear moduli (0.25-14.63 MPa), and 3D micro-cages (volume = 24 × 24 × 24 to 49 × 49 × 49 μm) with and without micro- and nano-pillar decorations (pillar diameters = 0.24-1 µm) were fabricated using two-photon polymerization (2PP). Compared to microglia cultured on flat substrates, cells growing on the pillar arrays exhibit an increased expression of the ramified phenotype and a higher number of primary branches per ramified cell. The interaction between the cells and the micro-pillar-decorated cages enables a more homogenous 3D cell colonization compared to the undecorated ones. The results pave the way for the development of improved primary microglia models to study these cells in both healthy and diseased conditions.
小胶质细胞是中枢神经系统中的常驻巨噬细胞,有助于维持大脑的内稳态。目前用于培养小胶质细胞的二维“培养皿”细胞培养平台无法体现天然脑组织的柔软度或拓扑结构。这常常导致小胶质细胞形态发生变化,呈现出阿米巴样表型,与健康脑组织中的稳态分支状表型有很大不同。为克服这一问题,首次开发并测试了多尺度工程化聚合物微环境,用于培养源自成年恒河猴的原代小胶质细胞。具体而言,利用双光子聚合技术(2PP)制备了仿生二维半微纳柱阵列(直径 = 0.29 - 1.06 µm),其有效剪切模量较低(0.25 - 14.63 MPa),以及有和没有微纳柱装饰(柱直径 = 0.24 - 1 µm)的三维微笼(体积 = 24×24×24至49×49×49 µm)。与在平坦基质上培养的小胶质细胞相比,在柱阵列上生长的细胞分支状表型的表达增加,每个分支状细胞的初级分支数量更多。与未装饰的笼子相比,细胞与微柱装饰笼子之间的相互作用使三维细胞定植更加均匀。这些结果为开发改进的原代小胶质细胞模型铺平了道路,以便在健康和患病条件下研究这些细胞。