open access publication

Article, 2024

Novel insights into the multifaceted and tissue-specific roles of the endocytic receptor LRP1

Journal of Biological Chemistry, ISSN 1083-351X, 0021-9258, Page 107521, 10.1016/j.jbc.2024.107521

Contributors

Yamamoto, Kazuhiro (Corresponding author) [1] Scilabra, Simone Dario 0000-0001-7300-6153 [2] Bonelli, Simone 0009-0003-7789-2502 [2] [3] Jensen, Anders M 0000-0003-1185-3343 [1] Scavenius, Carsten 0000-0002-4304-0681 [4] Enghild, Jan Johannes 0000-0001-9292-9172 [4] Strickland, Dudley K [5]

Affiliations

  1. [1] University of Liverpool
  2. [NORA names: United Kingdom; Europe, Non-EU; OECD];
  3. [2] Ri.MED
  4. [NORA names: Italy; Europe, EU; OECD];
  5. [3] University of Palermo
  6. [NORA names: Italy; Europe, EU; OECD];
  7. [4] Aarhus University
  8. [NORA names: AU Aarhus University; University; Denmark; Europe, EU; Nordic; OECD];
  9. [5] University of Maryland, Baltimore
  10. [NORA names: United States; America, North; OECD]

Abstract

Receptor-mediated endocytosis provides a mechanism for the selective uptake of specific molecules thereby controlling the composition of the extracellular environment and biological processes. The low-density lipoprotein receptor-related protein 1 (LRP1) is a widely expressed endocytic receptor that regulates cellular events by modulating the levels of numerous extracellular molecules via rapid endocytic removal. LRP1 also participates in signalling pathways through this modulation as well as in the interaction with membrane receptors and cytoplasmic adaptor proteins. LRP1 single nucleotide polymorphisms are associated with several diseases and conditions such as migraines, aortic aneurysms, cardiopulmonary dysfunction, corneal clouding, and bone dysmorphology and mineral density. Studies using Lrp1 knockout mice revealed a critical, non-redundant and tissue-specific role of LRP1 in regulating various physiological events. However, exactly how LRP1 functions to regulate so many distinct and specific processes is still not fully clear. Our recent proteomics studies have identified more than 300 secreted proteins that either directly interact with LRP1 or are modulated by LRP1 in various tissues. This review will highlight the remarkable ability of this receptor to regulate secreted molecules in a tissue-specific manner and discuss potential mechanisms underpinning such specificity. Uncovering the depth of these "hidden" specific interactions modulated by LRP1 will provide novel insights into a dynamic and complex extracellular environment that is involved in diverse biological and pathological processes.

Keywords

LRP1, Novel insights, adaptor protein, aneurysm, aortic aneurysm, associated with several diseases, biological processes, bone, bone dysmorphology, cardiopulmonary dysfunction, cellular events, cloud, complex extracellular environment, composition, conditions, corneal, corneal clouding, cytoplasmic adaptor proteins, density, depth, disease, dysfunction, dysmorphology, endocytic receptor, endocytic removal, endocytosis, environment, events, extracellular environment, extracellular molecules, insights, interaction, knockout mice, levels, lipoprotein receptor-related protein 1, low-density lipoprotein receptor-related protein 1, manner, mechanism, membrane, membrane receptors, mice, migraine, mineral density, modulation, molecules, non-redundant, nucleotide polymorphisms, pathological processes, pathway, physiological events, polymorphism, potential mechanisms, process, protein, protein 1, proteomic studies, proteomics, receptor low-density lipoprotein receptor-related protein 1, receptor-mediated endocytosis, receptors, regulate cellular events, removal, review, role, secreted proteins, severe disease, signal, signaling pathway, single nucleotide polymorphisms, specificity, study, tissue, tissue-specific manner, tissue-specific roles, uptake

Funders

  • Dunhill Medical Trust
  • Novo Nordisk Foundation
  • National Institute on Aging
  • The Velux Foundations
  • Versus Arthritis
  • National Heart Lung and Blood Institute

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