The central nervous system has a very limited capacity to regenerate damaged tissue. Therefore, regeneration strategies focus on transplantation of neural stem cells or differentiated neural cells. In order to make such a treatment effective, it is important to understand the mechanisms that enable cell differentiation. It is well known that besides biochemical cues, also mechanical and geometric properties of the cell environment, such as topography, curvature and stiffness, can influence the process, which has been studied mostly in 2D. In order to conduct relevant cell studies in vitro, it is therefore important to mimic the 3D structure of the in-vivo cell environment. Many different approaches have been adopted to create scaffolds for neuronal cells, such as freeze-drying, electrospinning and stereolitography. The main drawbacks of these methods are the limited resolution and the constraints in terms of achievable geometries. Two-photon polymerization overcomes these problems by using a laser to polymerize a photosensitive material in extremely confined volumes, achieving a submicrometric resolution. In this study, we fabricated 3D microscaffolds made of an acrylate polymer called IP-Dip by employing two-photon polymerization in order to study the effect of curved versus straight lattice geometries on the differentiation of mouse embryonic stem cells into neural progenitor cells. First, feasibility studies were carried out with HeLa cancer cells and the effect of curvature on these cells was investigated on 2.5D structures. We established a workflow for conducting these experiments from the fabrication up until the analysis. By employing confocal imaging, image stacks were obtained and then analysed to obtain the volumetric cell occupancy of the scaffolds and identify the location of the cells within the scaffolds. We concluded that mESCs could successfully grow and differentiate within the 3D scaffolds without a specific preference for a curved over a straight lattice structure.

Microglia, the resident macrophages of the central nervous system, are key players in neuroinflammation and neurodegenerative diseases, such as Alzheimer’s and Parkinson’s. These cells represent promising cellular targets for therapeutic intervention, therefore a detailed cellular biological knowledge of microglia is of paramount importance. Current microglia in vitro cell culture models are limited in their ability to recapitulate in vivo microglia in terms of gene expression and cell morphology. There is growing evidence that mimicking the cellular environment of microglia in the central nervous system will contribute to a more physiologically accurate culture model. Three-dimensional geometries, and physical and biochemical cues similar to the brain’s extracellular matrix, are necessary to create a 3D biomimetic in vitro environment, as microglia cells can sense these environmental cues through mechanosensing. In this thesis, the effect of two-photon polymerized 2.5D and 3D microstructures on microglia morphology and phenotype was studied through quantitative and qualitative cell analysis. Also, an attempt was made to create in vitro ramified microglia that resemble in vivo microglia from a morphological point of view, by con-trolling the effective shear modulus through dimensional optimization of compliant micro-and nanopillars. It was found that culturing microglia especially on nanopillars enabled an increase of the ramified pheno-type and a more complex (i.e. more ramifications) cell morphology as compared to microglia cultured onflat fused silica substrates. Furthermore, we report that microglia cultured on 3D structures exhibit similarphenotypes observed in the 2D and 2.5D cultures, and were more resemblingin vivomicroglia in terms of3D cell morphology.