Human and rat brain lipofuscin proteome

• Published in: Proteomics (Weinheim) Vol. 12; no. 15-16; pp. 2445 - 2454
• Main Authors: Ottis, Philipp, Koppe, Katharina, Onisko, Bruce, Dynin, Irina, Arzberger, Thomas, Kretzschmar, Hans, Requena, Jesus R., Silva, Christopher J., Huston, Joseph P., Korth, Carsten
• Format: Journal Article
• Language: English
• Published: Germany Blackwell Publishing Ltd 01.08.2012; Wiley Subscription Services, Inc
• Subjects: Aging; Animals; ATP synthase; Biomedicine; Brain - metabolism; Centrifugation, Density Gradient; Fluorescence; Fluorescence detection; Humans; Lipofuscin - metabolism; Macular degeneration; Mitochondria; Oxidative phosphorylation; Proteins; Proteome - metabolism; Rats; Rats, Wistar; Reproducibility of Results; Species Specificity
• ISSN: 1615-9853; 1862-8346; 1615-9861
• DOI: 10.1002/pmic.201100668

The accumulation of an autofluorescent pigment called lipofuscin in neurons is an invariable hallmark of brain aging. So far, this material has been considered to be waste material without particular relevance for cellular pathology. However, two lines of evidence argue that lipofuscin may play a yet unidentified role for pathological cellular functions: (i) Genetic forms of premature accumulation of similar autofluorescent material in neuronal ceroid lipofuscinosis indicate a direct disease‐associated link to lipofuscin; (ii) Retinal pigment epithelium cell lipofuscin is mechanistically linked to age‐associated macular degeneration. Here, we purified autofluorescent material from the temporal and hippocampal cortices of three different human individuals by a two‐step ultracentrifugation on sucrose gradients. For human brain lipofuscin, we could identify a common set of 49 (among > 200 total) proteins that are mainly derived from mitochondria, cytoskeleton, and cell membrane. This brain lipofuscin proteome was validated in an interspecies comparison with whole brain rat lipofuscin (total > 300 proteins), purified by the same procedure, yielding an overlap of 32 proteins (64%) between lipofuscins of both species. Our study is the first to characterize human and rat brain lipofuscin and identifies high homology, pointing to common cellular pathomechanisms of age‐associated lipofuscin accumulation despite the huge (40‐fold) difference in the lifespan of these species. Our identification of these distinct proteins will now allow research in disturbed molecular pathways during age‐associated dysfunctional lysosomal degradation.