The pericyte coverage ratio along the blood vasculature in cerebellar sections was quantified at three time periods in the EAE model (day 10–13, day 16, and day 21) and in naïve animals. Confocal images from cerebellar tissues stained to visualize pericytes, using the markers NG2 and PDGFRβ, and blood vessels through CD31, were assessed. Three naïve and three EAE animals were examined at each time point and three fields of view were quantified per animal. The pericyte coverage ratio was quantified by measuring the total length of the blood vessels in each field of view and the total length of the blood vessel covered by pericytes in each field of view. The pericyte coverage ratio in 60× confocal images having an area of 215 μm × 215 μm was calculated as follows:
To quantify pericyte density, the number of pericytes along the blood vasculature was quantified in each 60× confocal image, having an area of 215 μm × 215 μm.
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