Fig. 2From: Isolated nigral degeneration without pathological protein aggregation in autopsied brains with LRRK2 p.R1441H homozygous and heterozygous mutationsNeuronal loss and astrogliosis in the substantia nigra of cases with the LRRK2 p.R1441H mutation. A macroscopic picture of the midbrains (a: age-matched control, b: A-II-6, c: B-III-2). The substantia nigra of A-II-6 and B-III-2 were markedly depigmented, compared with the age-matched control (a macroscopic photograph of A-II-3 was not available). Black arrowheads indicate the pigmented nigral areas. The substantia nigra of all cases showed apparent neuronal loss and astrogliosis in hematoxylin and eosin (H&E) stain (d: A-II-3, e: A-II-6, f: B-III-2) and glial fibrillary acidic protein (GFAP) stain (g: A-II-3, h: A-II-6, i: B-III-2), but proliferations of reactive microglia were absent or mild (j: A-II-3, k: A-II-6, l: B-III-2). The scale bars represent d–f: 500 μm, g–i: 200 μm, and j–l: 200 μm, respectivelyBack to article page