Clusterin Is a Ligand for Apolipoprotein E Receptor 2 (ApoER2) and Very Low Density Lipoprotein Receptor (VLDLR) and Signals via the Reelin-signaling Pathway

Clusterin, also known as apolipoprotein J, is a multifunctional glycoprotein with the capacity to interact with a wide range of molecules. Although clusterin has been implicated in a broad spectrum of physiological and pathological processes, such as Alzheimer disease or cancer, its precise function...

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Published inThe Journal of biological chemistry Vol. 289; no. 7; pp. 4161 - 4172
Main Authors Leeb, Christian, Eresheim, Christine, Nimpf, Johannes
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 14.02.2014
American Society for Biochemistry and Molecular Biology
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Abstract Clusterin, also known as apolipoprotein J, is a multifunctional glycoprotein with the capacity to interact with a wide range of molecules. Although clusterin has been implicated in a broad spectrum of physiological and pathological processes, such as Alzheimer disease or cancer, its precise functions remain elusive. Here we report, that clusterin binds to apolipoprotein E receptor 2 (ApoER2) and very low density lipoprotein receptor (VLDLR) and is internalized by cells expressing either one of these receptors. Binding of clusterin to these receptors triggers a Reelin-like signal in cells expressing disabled-1 (Dab1). It induces phosphorylation of Dab1, which leads to activation of PI3K/Akt and n-cofilin. Cell proliferation and neuroblast chain formation in subventricular zone (SVZ) explants are compromised when clusterin, which is present in the subventricular zone, is blocked in vitro. These data suggest that in the subventricular zone where Reelin is not present but ApoER2, VLDLR, and Dab1, clusterin might be involved in maintaining neurogenesis in vivo. Clusterin is a highly conserved glycoprotein with broad tissue distribution but enigmatic biological functions. Clusterin signals via the lipoprotein receptors ApoER2 and VLDLR and stimulates cell proliferation in subventricular zone explants enabling neuronal outgrowth. Clusterin-mediated signaling is essential for neuronal chain formation in vitro. Discovery of a novel function of clusterin in neurogenesis.
AbstractList Clusterin, also known as apolipoprotein J, is a multifunctional glycoprotein with the capacity to interact with a wide range of molecules. Although clusterin has been implicated in a broad spectrum of physiological and pathological processes, such as Alzheimer disease or cancer, its precise functions remain elusive. Here we report, that clusterin binds to apolipoprotein E receptor 2 (ApoER2) and very low density lipoprotein receptor (VLDLR) and is internalized by cells expressing either one of these receptors. Binding of clusterin to these receptors triggers a Reelin-like signal in cells expressing disabled-1 (Dab1). It induces phosphorylation of Dab1, which leads to activation of PI3K/Akt and n-cofilin. Cell proliferation and neuroblast chain formation in subventricular zone (SVZ) explants are compromised when clusterin, which is present in the subventricular zone, is blocked in vitro. These data suggest that in the subventricular zone where Reelin is not present but ApoER2, VLDLR, and Dab1, clusterin might be involved in maintaining neurogenesis in vivo. Clusterin is a highly conserved glycoprotein with broad tissue distribution but enigmatic biological functions. Clusterin signals via the lipoprotein receptors ApoER2 and VLDLR and stimulates cell proliferation in subventricular zone explants enabling neuronal outgrowth. Clusterin-mediated signaling is essential for neuronal chain formation in vitro. Discovery of a novel function of clusterin in neurogenesis.
Clusterin, also known as apolipoprotein J, is a multifunctional glycoprotein with the capacity to interact with a wide range of molecules. Although clusterin has been implicated in a broad spectrum of physiological and pathological processes, such as Alzheimer disease or cancer, its precise functions remain elusive. Here we report, that clusterin binds to apolipoprotein E receptor 2 (ApoER2) and very low density lipoprotein receptor (VLDLR) and is internalized by cells expressing either one of these receptors. Binding of clusterin to these receptors triggers a Reelin-like signal in cells expressing disabled-1 (Dab1). It induces phosphorylation of Dab1, which leads to activation of PI3K/Akt and n-cofilin. Cell proliferation and neuroblast chain formation in subventricular zone (SVZ) explants are compromised when clusterin, which is present in the subventricular zone, is blocked in vitro. These data suggest that in the subventricular zone where Reelin is not present but ApoER2, VLDLR, and Dab1, clusterin might be involved in maintaining neurogenesis in vivo.
Background: Clusterin is a highly conserved glycoprotein with broad tissue distribution but enigmatic biological functions. Results: Clusterin signals via the lipoprotein receptors ApoER2 and VLDLR and stimulates cell proliferation in subventricular zone explants enabling neuronal outgrowth. Conclusion: Clusterin-mediated signaling is essential for neuronal chain formation in vitro . Significance: Discovery of a novel function of clusterin in neurogenesis. Clusterin, also known as apolipoprotein J, is a multifunctional glycoprotein with the capacity to interact with a wide range of molecules. Although clusterin has been implicated in a broad spectrum of physiological and pathological processes, such as Alzheimer disease or cancer, its precise functions remain elusive. Here we report, that clusterin binds to apolipoprotein E receptor 2 (ApoER2) and very low density lipoprotein receptor (VLDLR) and is internalized by cells expressing either one of these receptors. Binding of clusterin to these receptors triggers a Reelin-like signal in cells expressing disabled-1 (Dab1). It induces phosphorylation of Dab1, which leads to activation of PI3K/Akt and n-cofilin. Cell proliferation and neuroblast chain formation in subventricular zone (SVZ) explants are compromised when clusterin, which is present in the subventricular zone, is blocked in vitro . These data suggest that in the subventricular zone where Reelin is not present but ApoER2, VLDLR, and Dab1, clusterin might be involved in maintaining neurogenesis in vivo .
Author Nimpf, Johannes
Eresheim, Christine
Leeb, Christian
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BackLink https://www.ncbi.nlm.nih.gov/pubmed/24381170$$D View this record in MEDLINE/PubMed
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Issue 7
Keywords apoE Receptor 2
Cell Proliferation
Reelin
Lipoprotein Receptor
Cell Signaling
Apolipoproteins
Neurogenesis
Very Low Density Lipoprotein Receptor
Clusterin
Language English
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Snippet Clusterin, also known as apolipoprotein J, is a multifunctional glycoprotein with the capacity to interact with a wide range of molecules. Although clusterin...
Background: Clusterin is a highly conserved glycoprotein with broad tissue distribution but enigmatic biological functions. Results: Clusterin signals via the...
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proquest
crossref
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elsevier
SourceType Open Access Repository
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Index Database
Publisher
StartPage 4161
SubjectTerms Animals
apoE Receptor 2
Apolipoproteins
Cell Adhesion Molecules, Neuronal - genetics
Cell Adhesion Molecules, Neuronal - metabolism
Cell Biology
Cell Proliferation
Cell Signaling
Cells, Cultured
Clusterin
Clusterin - genetics
Clusterin - metabolism
Extracellular Matrix Proteins - genetics
Extracellular Matrix Proteins - metabolism
HEK293 Cells
Humans
LDL-Receptor Related Proteins - genetics
LDL-Receptor Related Proteins - metabolism
Lipoprotein Receptor
Mice
Midline Thalamic Nuclei - cytology
Midline Thalamic Nuclei - metabolism
Nerve Tissue Proteins - genetics
Nerve Tissue Proteins - metabolism
Neurogenesis
Neurogenesis - physiology
NIH 3T3 Cells
Receptors, LDL - genetics
Receptors, LDL - metabolism
Reelin
Reelin Protein
Serine Endopeptidases - genetics
Serine Endopeptidases - metabolism
Signal Transduction - physiology
Very Low Density Lipoprotein Receptor
Title Clusterin Is a Ligand for Apolipoprotein E Receptor 2 (ApoER2) and Very Low Density Lipoprotein Receptor (VLDLR) and Signals via the Reelin-signaling Pathway
URI https://dx.doi.org/10.1074/jbc.M113.529271
https://www.ncbi.nlm.nih.gov/pubmed/24381170
https://search.proquest.com/docview/1499148979
https://pubmed.ncbi.nlm.nih.gov/PMC3924281
Volume 289
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