The migratory abilities of motile human spermatozoa in vivo are essential for natural fertility, but it remains a mystery what properties distinguish the tens of cells which find an egg from the millions of cells ejaculated. To reach the site of fertilization, sperm must traverse narrow and convoluted channels, filled with viscous fluids. To elucidate individual and group behaviors that may occur in the complex three-dimensional female tract environment, we examine the behavior of migrating sperm in assorted microchannel geometries. Cells rarely swim in the central part of the channel cross-section, instead traveling along the intersection of the channel walls ("channel corners"). When the channel turns sharply, cells leave the corner, continuing ahead until hitting the opposite wall of the channel, with a distribution of departure angles, the latter being modulated by fluid viscosity. If the channel bend is smooth, cells depart from the inner wall when the curvature radius is less than a threshold value close to 150 μm. Specific wall shapes are able to preferentially direct motile cells. As a consequence of swimming along the corners, the domain occupied by cells becomes essentially one-dimensional, leading to frequent collisions, and needs to be accounted for when modeling the behavior of populations of migratory cells and considering how sperm populate and navigate the female tract. The combined effect of viscosity and three-dimensional architecture should be accounted for in future in vitro studies of sperm chemoattraction.cell swimming | motility | reproduction | thigmotaxis S perm motility is influenced by surfaces; this is most simply and strikingly evident in the accumulation of cells on the surfaces of microscope slides and coverslips, a phenomenon known to every andrologist. The effect and its causes have been investigated extensively through a variety of approaches, including microscopy (1-4), computational fluid mechanics, (5-9), molecular dynamics (10), and mathematical analysis (11). Principal points addressed by previous studies are the extent to which surface accumulation is a generic feature fluid dynamic effect associated with near-wall swimming, the role of specialized flagellar beat patterns, species-specific morphology, and the relative prevalence of swimming "near" as opposed to "against" walls; discussion of these questions can be found in recent editorials (12, 13). There has also been a resurgence of interest recently in the fluid mechanics of motile bacteria (14-17) and generic models for swimming cells (11,(18)(19)(20).Previous studies have usually focused on the behavior of a cell near a single planar surface or between a pair of planar surfaces, modeling the interior of a haemocytometer or similar device; however, both the female reproductive tract and microfluidic in vitro fertilization (IVF) devices present sperm with a much more confined and potentially tortuous geometry. The fallopian tubes consist of ciliated epithelium (21), the distance between opposed epithelial surfaces bein...