Because the uncontrolled adhesion of cells onto synthetic surfaces causes the malfunctioning of biomedical devices, the control of cell adhesion on artificial surfaces is of importance, especially in the biomedical field. Thus, various approaches have been developed to control cell adhesion on surfaces; among them, cell-resistant polymer coatings have extensively been utilized. Poly(ethylene glycol) and zwitterionic polymers are representative examples of polymers that display cell-resistant properties, and they have successfully been introduced onto a wide range of surfaces by appropriate immobilization techniques. With the growing interest in control over cell adhesion onto surfaces, another approach to achieving this goal has recently been developed, which is based on superhydrophobic surfaces. As hydrophobic coating of nanostructured surfaces has been identified as a key method for introducing the selfcleaningand superhydrophobic-surface properties of lotus leaves, both the construction and applications of biomimetic superhydrophobic surfaces have extensively been investigated. As a result, several promising properties, including the repellence of cells, have been reported. For instance, Lei et al. fabricated superhydrophobic surfaces by using aligned carbon nanotubes and reported that platelet adhesion was considerably reduced. Stratakis et al. investigated cell adhesion on nanostructured superhydrophobic surfaces as well, and concluded that the mammalian cell adhesion could be controlled by varying the roughness and wettability of the surface. The application of superhydrophobic surface has further advanced to the selective attachment of cells. Patterning of cells on superhydrophobic surfaces was, for instance, realized by site-specific UV/plasma treatment, giving rise to the hydrophilic/superhydrophobic patterning. Line-, circle-, and square-shaped hydrophilic patterns were fabricated on the surface, with the cell adherence only onto the hydrophilic region, resulting in spatio-selective cell adhesion. Although superhydrophobic surfaces have been applied to the preparation of cell patterns, the applied methods display several drawbacks with respect to practical use. They require external instruments for modifying the superhydrophobic surfaces. In addition, the methods are transient; the hydrophilicity decreases over time, eventually reverting to the original (hydrophobic) state. Therefore, a permanent method for modifying superhydrophobic surfaces is required. Indeed, recently, a facile and robust approach to modifying superhydrophobic surfaces was developed based on polydopamine coating. During polydopamine coating, dopamine is used to modify the surface under alkaline conditions, resulting in polydopamine-coated substrates. The advantage of this method is that it can be applied to any material surfaces, including superhydrophobic surfaces. Moreover, it is known that polydopamine-coated surfaces show excellent cell-adhesive properties. We, therefore, reasoned that polydopamine-coated superhydrophobic surfaces could provide efficient platforms for controlling cell adhesion. For the preparation of a superhydrophobic surface, anodized aluminum oxide was used as a nanostructured surface onto which hydrophobic fluorosilane was deposited. After preparation, the surface was selectively coated with polydopamine to induce cell-adhesive properties. Selective polydopamine coating was performed by half-masking the surface using a polydimethylsiloxane (PDMS) slab, which was carefully removed after 18-h coating (Figure 1). Modification of the superhydrophobic surface by polydopamine was characterized by water-contact angle measurements. The significant change in the angle from 157.5 ± 3.0 to 36.3 ± 1.4 indicated that the surface was successfully modified by a layer of polydopamine (Figure 2). The surface was further analyzed by X-ray photoelectron spectroscopy (XPS). The unmodified superhydrophobic surface showed an intense CF2 peak at 291 eV, originating from the hydrophobic fluorosilane layers. After polydopamine coating, a decrease in intensity of the peak at 291 eV was observed, and the peak at 284 eV, corresponding to the C 1s of the polydopamine