(A) Time-lapse images taken in a DA animal showing a microglial process that terminates into a structurally stable phagocytic cup (white arrow), while another process dynamically contacts two dendritic spines (red arrowheads before the contact; white arrowheads during the contact). Scale bar = 5 µm. (B) Time-lapse images showing another example of a structurally stable phagocytic cup (white arrow) in a DA animal. Scale bar = 10 µm. (C) Time-lapse images showing the motility of microglia during normal visual experience over three time points, 0, 5, and 25 min. Images from each time point were colored in red, green, and blue, respectively, and then merged to reveal microglia-associated pixels that were unchanged throughout the three time points (stable; white), changed in one of the three time points (dynamic; yellow and fuchsia), or changed in two of the three time points (highly dynamic; red, green, or blue). Scale bar = 10 µm. (D) Change in microglial motility index during DA and DA+light, measured as the proportion of the pixels that differed between images of a single microglia taken 5 or 25 min apart (mean±SEM). Black asterisks refer to comparisons with control animals, and green or blue asterisks to comparisons with DA animals. (E) Initial size of non-contacted and contacted dendritic spines in control, DA, and DA+light animals (mean ± SEM). Black asterisks refer to comparisons with non-contacted spines in control animals, dark grey asterisks to comparisons with non-contacted spines in DA animals, and light grey asterisks to comparisons with non-contacted spines in animals reexposed to light. (F) Dendritic spine size before, during, and after microglial contact in DA animals (left) and DA+light animals (right). Data were normalized to the first condition for presentation purposes. *, p<0.05; **, p<0.01; ***, p<0.001. See also Figures S11 and S12, as well as Videos S2, S3, S5, and S6.