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. Author manuscript; available in PMC: 2010 Jul 1.
Published in final edited form as: J Neuropathol Exp Neurol. 2009 Jul;68(7):785–796. doi: 10.1097/NEN.0b013e3181aaf4fd

Figure 4.

Figure 4

Leucine-rich repeat kinase-2 (LRRK2) expression or aggregate formation does not change levels of GFP-u. LRRK2-V5 was used to transfect cells that stably express a short-lived GFP that is degraded by the proteasome (GFP-u). Double immunofluorescence was performed between a monoclonal anti-V5 antibody (red) and GFP (green). Under basal conditions (A), cells with aggregates (arrows) do not increase GFP fluorescence. (B) MG132 treatment (10 µM, 16 hours) increased GFP fluorescence of all cells. GFP colocalized with LRRK2 aggregates in some cells (arrowhead). Images are representative of 3 independent experiments. Bar scale: 50 µm.