The DOI matches its Crossref record; 202 of the 202 references it cites were found in a registry or an index.
Lipoprotein Receptors in the Nervous System
Abstract
The low-density-lipoprotein (LDL) receptor family is an evolutionarily ancient gene family of structurally closely related cell-surface receptors. Members of the family are involved in the cellular uptake of extracellular ligands and regulate diverse biological processes including lipid and vitamin metabolism and cell-surface protease activity. Some members of the family also participate in cellular signaling and regulate the development and functional maintenance of the nervous system. Here we review the roles of this family of multifunctional receptors in the nervous system and focus on recent advances toward the understanding of the mechanisms by which lipoprotein receptors and their ligands transmit and modulate signals in the brain.
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ApoE binds to a group of structurally related proteins known as the LDL receptor family.
“ApoE binds to a group of structurally related proteins known as the low density lipoprotein receptor (LDLR) family.”
From Overexpression of Low-Density Lipoprotein Receptor in the Brain Markedly Inhibits Amyloid Deposition and Increases Extracellular Aβ Clearance (2009) · cites this paper as Herz and Bock, 2002
VLDLR and ApoER2 share the highest overall sequence homology with LDLR among the LDLR family.
“Among the LDLR family of proteins, the VLDLR (very low density lipoprotein receptor) and ApoER2 (also known as LRP8) share the highest overall sequence homology with the LDLR (14).”
From The E3 ubiquitin ligase IDOL induces the degradation of the low density lipoprotein receptor family members VLDLR and ApoER2 (2010) · cites this paper as [14]
The high degree of evolutionary conservation within the LDLR family of receptors prompted the investigation of substrate specificity of IDOL.
“Our investigation of the substrate specificity of IDOL was largely prompted by the high degree of evolutionary conservation within the LDLR family of receptors (14).”
From The E3 ubiquitin ligase IDOL induces the degradation of the low density lipoprotein receptor family members VLDLR and ApoER2 (2010) · cites this paper as [14]
ApoE receptors are members of the low-density lipoprotein receptor gene family that play important roles in maintaining the proper function of neurons.
“ApoE receptors are members of the low-density lipoprotein receptor gene family that play important roles in maintaining the proper function of neurons (Herz and Bock, 2002).”
From The E3 ubiquitin ligase IDOL regulates synaptic ApoER2 levels and is important for plasticity and learning (2017) · cites this paper as Herz and Bock, 2002
The ligands for LRP1 include several proteins already implicated in AD pathogenesis, such as apoE, APP, Aβ, α2-macroglobulin, matrix metallopeptidase 9, and tissue-type plasminogen activator.
“The ligands for LRP1 include several proteins already implicated in AD pathogenesis, such as apoE, APP, Aβ, α2-macroglobulin, matrix metallopeptidase 9, and tissue-type plasminogen activator (Herz and Bock, 2002).”
From The role of apolipoprotein E in Alzheimer's disease (2009) · cites this paper as Herz and Bock, 2002
LRP1 functions as an endocytic and signaling receptor with a wide expression pattern in a variety of tissues.
“LRP1 functions as an endocytic and signaling receptor with a wide expression pattern in a variety of tissues.”
From The role of apolipoprotein E in Alzheimer's disease (2009) · cites this paper as Herz and Bock, 2002
LDLR is a cell surface glycoprotein that plays an important role in mediating the removal of cholesterol and cholesteryl ester-containing low-density lipoprotein particles from the circulation.
“LDLR is a cell surface glycoprotein that plays an important role in mediating the removal of cholesterol and cholesteryl ester-containing low-density lipoprotein (LDL) particles from the circulation (Brown and Goldstein, 1986; Herz and Bock, 2002).”
From The role of apolipoprotein E in Alzheimer's disease (2009) · cites this paper as Herz and Bock, 2002
LRP is a multiligand endocytic receptor and a member of the LDL receptor family.
“The LDL receptor-related protein (LRP) is a multiligand endocytic receptor that belongs to the LDL receptor family (Herz and Bock, 2002).”
From Sorting nexin 17 facilitates LRP recycling in the early endosome (2005) · cites this paper as Herz and Bock, 2002
LRP1 is a transmembrane receptor that belongs to the LDLR family.
“The low-density lipoprotein receptor (LDLR)-related protein 1 (LRP1) is a transmembrane receptor that belongs to the LDLR family [20].”
From LRP1 is a neuronal receptor for α-synuclein uptake and spread (2022) · cites this paper as [20]
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Metadata
- Authors
- Herz, J., & Bock, H. H.
- Affiliations
- The University of Texas Southwestern Medical Center (US)
- Venue
- Annual Review of Biochemistry
- Publisher
- Annual Reviews
- Published
- 2002-06
- Volume
- 71
- Issue
- 1
- Pages
- 405-434
- ISSN
- 0066-4154 (ISSN-L)
- 1545-4509
- OpenAlex
- W2149816215
- Cited by
- 457
- References
- 202
- Citations by year
- 2026: 6 · 2025: 12 · 2024: 14 · 2023: 18 · 2022: 19 · 2021: 11 · 2020: 16 · 2019: 13 · 2018: 10 · 2017: 8 · 2016: 11 · 2015: 8 · 2014: 21 · 2013: 12 · 2012: 20
- FWCI
- 6.54
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Annual Review of Biochemistry (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institutes of Health
- National Heart, Lung, and Blood Institute (R37HL063762)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Biochemistry › Cholesterol and Lipid Metabolism
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Alzheimer's disease research and treatments
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Keywords
- low-density lipoprotein receptor family, lipoprotein receptors, nervous system, brain, receptor signaling, lipid metabolism, vitamin metabolism, proteolytic activity, cell surface receptors, brain development, neuroprotection
- MeSH terms
- Reelin Protein, Animals, Apolipoproteins E, Brain, Central Nervous System, Cholesterol, Multigene Family, Learning, Ligands, Nerve Tissue Proteins, Proto-Oncogene Proteins, Receptors, LDL, Serine Endopeptidases, Signal Transduction, Trans-Activators, Cell Adhesion Molecules, Neuronal, Receptors, N-Methyl-D-Aspartate, Extracellular Matrix Proteins, Protein Transport, Caveolae, Membrane Microdomains, Zebrafish Proteins, Wnt Proteins, Hedgehog Proteins
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
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