The local heating of poly(3,4-ethylenedioxythiophene) (PEDOT) by ap hotothermal effect directed by nearinfrared (NIR) light induces unfolding of absorbed collagen triple helices,yielding soluble collagen single-helical structures. This dissociation of collagens allowed the harvesting of aliving idiomorphic cell sheet, achieved upon irradiation with NIR light (l = 808 nm). The PEDOTlayer was patterned and cells were successfully cultured on the patterned substrate.C ell sheets of various shapes mirroring the PEDOTp attern could be detached after af ew minutes of irradiation with NIR light. The PEDOTp atterns guided not only the entire shape of the cell sheets but also the spreading direction of the cells in the sheets.T his photothermally induced dissociation of collagen provided af ast non-invasive harvesting method and tailormade cell-sheet patterns.Collagen, which has at riple-helical structure,i st he one of the most important proteins in cell science. [1][2][3][4] Each triple helixisstabilized by numerous hydrogen bonds and supports cell binding.H owever,t he triple helix of collagens unfolds upon heating. [5] Therefore,c ontrolling the dissociation of collagen could be highly important for cell-to-surface interactions and eventually for the detachment of cells.Most celldetachment studies are undertaken using temperatureresponsive culture dishes on which thermoresponsive polymers,s uch as poly(N-isopropylacrylamide) (pNIPAAm), are covalently grafted. [6][7][8][9][10] Although this is one of the most promising methods and is well-established, spatial control of dissociation is particularly difficult using these thermoresponsive substrates.N ear-IR (NIR) laser irradiation is "biologically friendly" and can be employed to provide au nique method to spatially control cell behavior. [11][12][13][14] By spatially dissociating collagens through the photothermal effect, we now describe,for the first time,tunable cell-sheet detachment and harvesting from ap oly(3,4-ethylenedioxythiophene) (PEDOT) substrate without achange in the cell morphology.PEDOTwas directly coated onto polystyrene by polymer solution casting to form SP-PEDOT (PEDOT made by solution casting polymerization (SP)). Then collagen type I (0.3 wt %) was dropcast onto the SP-PEDOT substrate.T he thickness of the collagen layer was 14-18 mm, as determined using an Alpha-Step surface profiler.Fibroblasts were seeded on top of ac ollagen-coated PEDOT substrate (CSP-PEDOT) at ac oncentration of 310 5 cells/dish and were cultured for 3days.T he CSP-PEDOTw as irradiated with aN IR diode laser (l = 808 nm), with an input power density (I pw )between 1.9 Wcm À2 and 2.5 Wcm À2 (see Table S1 in the Supporting Information). When exposed to NIR light, the temperature of the CSP-PEDOTw as increased to 41.4 8 8C ( Figure S1). After 5min of irradiation, the cell sheets were detached from the substrate (Figure 1a). Theh arvested cell sheets showed positive E-cadherin expression (Figure 1b), verifying that cell-cell interactions are maintained in the harvested cell sheet...