Bruch's membrane compartmentalises complement regulation in the eye with implications for therapeutic design in age-related macular degeneration.

摘要

Age-related macular degeneration (AMD) is the leading cause of blindness in the western world and affects nearly 200 million peopleglobally. Local inflammation driven by complement system dysregulation is currently a therapeutic target. Bruch’s membrane(BrM) is a sheet of extracellular matrix that separates the retina from the underlying choroid, a highly vascularized layer thatsupplies oxygen and nutrition to the outer retina. Here we show that most complement proteins are unable to diffuse throughBrM, although FHL-1, factor D and C5a can. AMD-associated lipid deposition in BrM decreases FHL-1 diffusion. We show that thisimpermeability of BrM creates two separate semi-independent compartments with respect to complement activation andregulation. Complement proteins synthesized locally on either side of BrM, or on the choroidal side if derived from the circulation,predominantly remain on their side of origin. As previous studies suggest that complement activation in AMD is confined to thechoroidal side of BrM we propose a model whereby complement activation in the choriocapillaris layer of the choroid generatesC5a, which crosses BrM to interact with its specific receptor on RPE cells to initiate an inflammatory response in the retina.Understanding mechanisms underpinning AMD is essential for developing therapeutics that target the right molecule in the rightanatomical compartment.