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RESEARCH PAPER / 2025-04-21

Separation of powers: A key feature underlying the neuroprotective role of Retromer in age-related neurodegenerative disease?

Brett M Collins, Peter J Cullen

The University of Queensland, Institute for Molecular Bioscience, St Lucia, Queensland, 4072, Australia. Electronic address: [email protected]. · pubmed

Abstract

The retromer complex was discovered in Saccharomyces cerevisiae as a multiprotein, pentameric assembly essential for recycling of integral membrane cargo proteins through the endosomal network [1,2]. We now understand how retromer is assembled, its membrane architecture, and how it selects proteins for recycling [3-6]. Conserved across eukaryotes, analyses have revealed retromer's role in organism development, and homeostasis and has linked retromer defects with age-related Alzheimer's disease and Parkinson's disease and other neurological disorders [3,5,7]. Indeed, stabilizing retromer function is now actively considered a therapeutic strategy [8]. Here, we reflect on its structural and functional evolution rather than overviewing retromer biology (see, e.g. [5,7]). Specifically, we clarify the organization of the human retromer to provide greater focus for future research, especially within the context of retromer's function in neuroprotection.

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Research summary

The paper claims that understanding the structural and functional evolution of the retromer complex can provide insights into its neuroprotective role in age-related neurodegenerative diseases. The relevance stems from its focus on retromer's potential therapeutic implications in addressing the underlying mechanisms of neurodegeneration associated with aging.

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