{Reference Type}: Journal Article
{Title}: Integrative proteomics identifies a conserved Aβ amyloid responsome, novel plaque proteins, and pathology modifiers in Alzheimer's disease.
{Author}: Levites Y;Dammer EB;Ran Y;Tsering W;Duong D;Abreha M;Gadhavi J;Lolo K;Trejo-Lopez J;Phillips J;Iturbe A;Erquizi A;Moore BD;Ryu D;Natu A;Dillon K;Torrellas J;Moran C;Ladd T;Afroz F;Islam T;Jagirdar J;Funk CC;Robinson M;Rangaraju S;Borchelt DR;Ertekin-Taner N;Kelly JW;Heppner FL;Johnson ECB;McFarland K;Levey AI;Prokop S;Seyfried NT;Golde TE;
{Journal}: Cell Rep Med
{Volume}: 5
{Issue}: 8
{Year}: 2024 Aug 20
{Factor}: 16.988
{DOI}: 10.1016/j.xcrm.2024.101669
{Abstract}: Alzheimer's disease (AD) is a complex neurodegenerative disorder that develops over decades. AD brain proteomics reveals vast alterations in protein levels and numerous altered biologic pathways. Here, we compare AD brain proteome and network changes with the brain proteomes of amyloid β (Aβ)-depositing mice to identify conserved and divergent protein networks with the conserved networks identifying an Aβ amyloid responsome. Proteins in the most conserved network (M42) accumulate in plaques, cerebrovascular amyloid (CAA), and/or dystrophic neuronal processes, and overexpression of two M42 proteins, midkine (Mdk) and pleiotrophin (PTN), increases the accumulation of Aβ in plaques and CAA. M42 proteins bind amyloid fibrils in vitro, and MDK and PTN co-accumulate with cardiac transthyretin amyloid. M42 proteins appear intimately linked to amyloid deposition and can regulate amyloid deposition, suggesting that they are pathology modifiers and thus putative therapeutic targets. We posit that amyloid-scaffolded accumulation of numerous M42+ proteins is a central mechanism mediating downstream pathophysiology in AD.