Table 2.
A summary of reports in the literature for topography-driven cell response: cytoskeleton organization and differentiation with respect to the shape and size of the topography.
Substrate material | Type of topography | Width/diameter | Height | Cell type | Cell Response | Ref. |
---|---|---|---|---|---|---|
PMMA | Dot | 140–2200 nm | 11–45 nm | Human mesenchymal stem cells | Increased FA formation on nanodots, bone nodules formed on 45 nm high dots | [17] |
Ti/TiO2 | Dot | 20–55.5 nm | 30–115 nm | Human mesenchymal stem cells | Increased cytoskeleton organization, Focal adhesion size | [18] |
PCL | Pit | 20/30/40 μm | 300 nm | Primary human osteoblasts | Increased cytoskeleton spreading and FA formation | [19] |
PDMS coated | Pit | 3 μm | 2–4 μm | Murine mesenchymal stem cells | Increased FA size, actin polymerization and osteogenic differentiation | [20] |
PMMA | Groove | 10, 25, 100 μm | 330 nm | Mesenchymal stem cells | Increased FA formation and osteoblastic differentiation | [21] |
PC | Grooves | 2 μm | 7 μm | Osteoblasts | Decreased osteoblastic differentiation and FAs on grooved surfaces vs. flat surfaces | [22] |
Ti | Groove | 0.5–50 μm | 1.3 μm | Mesenchymal stem cells | Increased cell attachment and spreading vs. flat surface. Larger cell adhesion density on narrower grooves (0.5 and 0.75 μm wide grooves) | [23] |
Stainless steel | Groove | 40, 50, 80 μm | ~5–20 μm | Primary osteoblasts | Increased mineralization and alignment of collagen. | [24] |
Polyimide | Microgroove | 4 μm | 5 μm | Osteoblasts | Strong elongation and alignment | [25] |
PMMA | Nanogroove | 10, 25, 100 μm | 330 nm | Human osteoblasts | Decreased nanogroove widths led to increased contact guidance, decreased adhesion and increased angiogenic gene expressions | [26] |
PS | Microgroove | 1–10 μm | 0.5–1.5 μm | Rat bone marrow cells | On large grooves, focal adhesions cover the surface, | [27] |
PHBV | Microchannel | 1–10 μm | 5–30 μm | Rat mesenchymal stem cell-derived osteoblasts | Increased osteoblast adhesion and alignment | [28] |
Collagen | Microchannel | 27 μm | 12 μm | Mesenchymal osteoprogenitor cells | Cell alignment facilitated enhanced bone formation | [29] |
Collagen coated fibrinogen | Microgroove | 27 μm | 12 μm | Rat bone marrow osteoblast cells | Enhanced cell orientation and bone formation | [30] |
PMMA | Micropillar | 4, 8, 16 μm | 8 μm | Dental pulm mesenchymal stem cells | 8 μm height of the pillars showed enhanced osteogenic differentiation | [31] |
PLGA | Micropillar | 3 μm | 7 μm | Mesenchymal stem cells | The geometry of cell nuclei responds to the micropillar array | [32] |
PLGA | Micropillar | 3 μm | 5 μm | Bone marrow stromal cells | Reduced height showed severe nucleus deformation, but no change in proliferation and differentiation of bone marrow stromal cells | [33] |
Ti | Micropillar | 21 nm | 15 nm | Bone marrow stromal cells | Improved bone deposition on nanopillars | [34] |
PMMA | Nanopits | 120 nm | 100 nm | Mesenchymal stem cells | Stimulated differentiation and production of bone mineral in vitro | [35] |
Ti | Micropits | 100, 30, 10 μm | Osteoblast like cells | Cell attachment, growth, aggregation and morphology depends on the presence and dimension of the micropatterns | [36] | |
PCL | microwells | 30 μm | 80, 220, 333 nm | Bone marrow stromal cells | Optimal adhesion on 80 nm deep pits, inductive capability on 220 nm deep pits | [37] |
PMMA: polymethylmethacrylate, PDMS: polydimethylsiloxane, PLLA: polylactic acid, PUA: polyurethane, PCL: polycaprolactone, PC: polycarbonate, PS: polystyrene, PLGA: polylactic glycolic acid. PS Polystyrene.