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Published in: NeuroMolecular Medicine 2-3/2017

01-09-2017 | Original Paper

Low-Density Lipoprotein Receptor-Related Protein-1 (LRP1) C4408R Mutant Promotes Amyloid Precursor Protein (APP) α-Cleavage in Vitro

Authors: Huayan Hou, Ahsan Habib, Dan Zi, Kathy Tian, Jun Tian, Brian Giunta, Darrell Sawmiller, Jun Tan

Published in: NeuroMolecular Medicine | Issue 2-3/2017

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Abstract

Previous studies have demonstrated that the low-density lipoprotein receptor-related protein-1 (LRP1) plays conflicting roles in Alzheimer’s disease (AD) pathogenesis, clearing β-amyloid (Aβ) from the brain while also enhancing APP endocytosis and resultant amyloidogenic processing. We have recently discovered that co-expression of mutant LRP1 C-terminal domain (LRP1-CT C4408R) with Swedish mutant amyloid precursor protein (APPswe) in Chinese hamster ovary (CHO) cells decreases Aβ production, while also increasing sAPPα and APP α-C-terminal fragment (α-CTF), compared with CHO cells expressing APPswe alone. Surprisingly, the location of this mutation on LRP1 corresponded with the α-secretase cleavage site of APP. Further experimentation confirmed that in CHO cells expressing APPswe or wild-type APP (APPwt), co-expression of LRP1-CT C4408R decreases Aβ and increases sAPPα and α-CTF compared with co-expression of wild-type LRP1-CT. In addition, LRP1-CT C4408R enhanced the unglycosylated form of LRP1-CT and reduced APP endocytosis as determined by flow cytometry. This finding identifies a point mutation in LRP1 which slows LRP1-CT-mediated APP endocytosis and amyloidogenic processing, while enhancing APP α-secretase cleavage, thus demonstrating a potential novel target for slowing AD pathogenesis.
Literature
go back to reference Bading, J. R., et al. (2002). Brain clearance of Alzheimer’s amyloid-beta40 in the squirrel monkey: A SPECT study in a primate model of cerebral amyloid angiopathy. Journal of Drug Targeting, 10(4), 359–368.CrossRefPubMed Bading, J. R., et al. (2002). Brain clearance of Alzheimer’s amyloid-beta40 in the squirrel monkey: A SPECT study in a primate model of cerebral amyloid angiopathy. Journal of Drug Targeting, 10(4), 359–368.CrossRefPubMed
go back to reference Bell, R. D., et al. (2009). SRF and myocardin regulate LRP-mediated amyloid-beta clearance in brain vascular cells. Nature Cell Biology, 11(2), 143–153.CrossRefPubMed Bell, R. D., et al. (2009). SRF and myocardin regulate LRP-mediated amyloid-beta clearance in brain vascular cells. Nature Cell Biology, 11(2), 143–153.CrossRefPubMed
go back to reference Boucher, P., & Herz, J. (2011). Signaling through LRP1: Protection from atherosclerosis and beyond. Biochemical Pharmacology, 81(1), 1–5.CrossRefPubMed Boucher, P., & Herz, J. (2011). Signaling through LRP1: Protection from atherosclerosis and beyond. Biochemical Pharmacology, 81(1), 1–5.CrossRefPubMed
go back to reference Bu, G., et al. (2006). LRP in amyloid-beta production and metabolism. Annals of the New York Academy of Sciences, 1086, 35–53.CrossRefPubMed Bu, G., et al. (2006). LRP in amyloid-beta production and metabolism. Annals of the New York Academy of Sciences, 1086, 35–53.CrossRefPubMed
go back to reference Cam, J. A., et al. (2005). Rapid endocytosis of the low density lipoprotein receptor-related protein modulates cell surface distribution and processing of the beta-amyloid precursor protein. Journal of Biological Chemistry, 280(15), 15464–15470.CrossRefPubMed Cam, J. A., et al. (2005). Rapid endocytosis of the low density lipoprotein receptor-related protein modulates cell surface distribution and processing of the beta-amyloid precursor protein. Journal of Biological Chemistry, 280(15), 15464–15470.CrossRefPubMed
go back to reference Deane, R., et al. (2004). LRP/amyloid beta-peptide interaction mediates differential brain efflux of Abeta isoforms. Neuron, 43(3), 333–344.CrossRefPubMed Deane, R., et al. (2004). LRP/amyloid beta-peptide interaction mediates differential brain efflux of Abeta isoforms. Neuron, 43(3), 333–344.CrossRefPubMed
go back to reference Deane, R., et al. (2008). apoE isoform-specific disruption of amyloid beta peptide clearance from mouse brain. The Journal of Clinical Investigation, 118(12), 4002–4013.CrossRefPubMedPubMedCentral Deane, R., et al. (2008). apoE isoform-specific disruption of amyloid beta peptide clearance from mouse brain. The Journal of Clinical Investigation, 118(12), 4002–4013.CrossRefPubMedPubMedCentral
go back to reference DeMattos, R. B., et al. (2004). ApoE and clusterin cooperatively suppress Abeta levels and deposition: Evidence that ApoE regulates extracellular Abeta metabolism in vivo. Neuron, 41(2), 193–202.CrossRefPubMed DeMattos, R. B., et al. (2004). ApoE and clusterin cooperatively suppress Abeta levels and deposition: Evidence that ApoE regulates extracellular Abeta metabolism in vivo. Neuron, 41(2), 193–202.CrossRefPubMed
go back to reference Deng, J., et al. (2015). Soluble amyloid precursor protein alpha inhibits tau phosphorylation through modulation of GSK3beta signaling pathway. Journal of Neurochemistry, 135(3), 630–637.CrossRefPubMedPubMedCentral Deng, J., et al. (2015). Soluble amyloid precursor protein alpha inhibits tau phosphorylation through modulation of GSK3beta signaling pathway. Journal of Neurochemistry, 135(3), 630–637.CrossRefPubMedPubMedCentral
go back to reference Dieckmann, M., et al. (2010). Lipoprotein receptors—An evolutionarily ancient multifunctional receptor family. Biological Chemistry, 391(11), 1341–1363.CrossRefPubMedPubMedCentral Dieckmann, M., et al. (2010). Lipoprotein receptors—An evolutionarily ancient multifunctional receptor family. Biological Chemistry, 391(11), 1341–1363.CrossRefPubMedPubMedCentral
go back to reference Donahue, J. E., et al. (2006). RAGE, LRP-1, and amyloid-beta protein in Alzheimer’s disease. Acta Neuropathologica, 112(4), 405–415.CrossRefPubMed Donahue, J. E., et al. (2006). RAGE, LRP-1, and amyloid-beta protein in Alzheimer’s disease. Acta Neuropathologica, 112(4), 405–415.CrossRefPubMed
go back to reference Hardy, J., & Selkoe, D. J. (2002). The amyloid hypothesis of Alzheimer’s disease: Progress and problems on the road to therapeutics. Science, 297(5580), 353–356.CrossRefPubMed Hardy, J., & Selkoe, D. J. (2002). The amyloid hypothesis of Alzheimer’s disease: Progress and problems on the road to therapeutics. Science, 297(5580), 353–356.CrossRefPubMed
go back to reference Herring, A., et al. (2008). Environmental enrichment counteracts Alzheimer’s neurovascular dysfunction in TgCRND8 mice. Brain Pathology, 18(1), 32–39.CrossRefPubMed Herring, A., et al. (2008). Environmental enrichment counteracts Alzheimer’s neurovascular dysfunction in TgCRND8 mice. Brain Pathology, 18(1), 32–39.CrossRefPubMed
go back to reference Herz, J., & Strickland, D. K. (2001). LRP: A multifunctional scavenger and signaling receptor. The Journal of Clinical Investigation, 108(6), 779–784.CrossRefPubMedPubMedCentral Herz, J., & Strickland, D. K. (2001). LRP: A multifunctional scavenger and signaling receptor. The Journal of Clinical Investigation, 108(6), 779–784.CrossRefPubMedPubMedCentral
go back to reference Hussain, M. M., et al. (1999). The mammalian low-density lipoprotein receptor family. Annual Review of Nutrition, 19, 141–172.CrossRefPubMed Hussain, M. M., et al. (1999). The mammalian low-density lipoprotein receptor family. Annual Review of Nutrition, 19, 141–172.CrossRefPubMed
go back to reference Kimberly, W. T., et al. (2003). Gamma-secretase is a membrane protein complex comprised of presenilin, nicastrin, Aph-1, and Pen-2. Proceedings of the National Academy of Sciences USA, 100(11), 6382–6387.CrossRef Kimberly, W. T., et al. (2003). Gamma-secretase is a membrane protein complex comprised of presenilin, nicastrin, Aph-1, and Pen-2. Proceedings of the National Academy of Sciences USA, 100(11), 6382–6387.CrossRef
go back to reference Koo, E. H., & Squazzo, S. L. (1994). Evidence that production and release of amyloid beta-protein involves the endocytic pathway. Journal of Biological Chemistry, 269(26), 17386–17389.PubMed Koo, E. H., & Squazzo, S. L. (1994). Evidence that production and release of amyloid beta-protein involves the endocytic pathway. Journal of Biological Chemistry, 269(26), 17386–17389.PubMed
go back to reference Kounnas, M. Z., et al. (1995). LDL receptor-related protein, a multifunctional ApoE receptor, binds secreted beta-amyloid precursor protein and mediates its degradation. Cell, 82(2), 331–340.CrossRefPubMed Kounnas, M. Z., et al. (1995). LDL receptor-related protein, a multifunctional ApoE receptor, binds secreted beta-amyloid precursor protein and mediates its degradation. Cell, 82(2), 331–340.CrossRefPubMed
go back to reference Lefort, R., et al. (2012). Cross-linking of cell surface amyloid precursor protein leads to increased beta-amyloid peptide production in hippocampal neurons: Implications for Alzheimer’s disease. Journal of Neuroscience, 32(31), 10674–10685.CrossRefPubMedPubMedCentral Lefort, R., et al. (2012). Cross-linking of cell surface amyloid precursor protein leads to increased beta-amyloid peptide production in hippocampal neurons: Implications for Alzheimer’s disease. Journal of Neuroscience, 32(31), 10674–10685.CrossRefPubMedPubMedCentral
go back to reference Li, S., et al. (2015). Swedish mutant APP-based BACE1 binding site peptide reduces APP β-cleavage and cerebral Aβ levels in Alzheimer’s mice. Scientific Reports, 5, 11322.CrossRefPubMedPubMedCentral Li, S., et al. (2015). Swedish mutant APP-based BACE1 binding site peptide reduces APP β-cleavage and cerebral Aβ levels in Alzheimer’s mice. Scientific Reports, 5, 11322.CrossRefPubMedPubMedCentral
go back to reference Lillis, A. P., et al. (2008). LDL receptor-related protein 1: Unique tissue-specific functions revealed by selective gene knockout studies. Physiological Reviews, 88(3), 887–918.CrossRefPubMedPubMedCentral Lillis, A. P., et al. (2008). LDL receptor-related protein 1: Unique tissue-specific functions revealed by selective gene knockout studies. Physiological Reviews, 88(3), 887–918.CrossRefPubMedPubMedCentral
go back to reference Moestrup, S. K., et al. (1992). Distribution of the alpha 2-macroglobulin receptor/low density lipoprotein receptor-related protein in human tissues. Cell and Tissue Research, 269(3), 375–382.CrossRefPubMed Moestrup, S. K., et al. (1992). Distribution of the alpha 2-macroglobulin receptor/low density lipoprotein receptor-related protein in human tissues. Cell and Tissue Research, 269(3), 375–382.CrossRefPubMed
go back to reference Narita, M., et al. (1997). Alpha2-macroglobulin complexes with and mediates the endocytosis of beta-amyloid peptide via cell surface low-density lipoprotein receptor-related protein. Journal of Neurochemistry, 69(5), 1904–1911.CrossRefPubMed Narita, M., et al. (1997). Alpha2-macroglobulin complexes with and mediates the endocytosis of beta-amyloid peptide via cell surface low-density lipoprotein receptor-related protein. Journal of Neurochemistry, 69(5), 1904–1911.CrossRefPubMed
go back to reference Neels, J. G., et al. (1999). The second and fourth cluster of class A cysteine-rich repeats of the low density lipoprotein receptor-related protein share ligand-binding properties. Journal of Biological Chemistry, 274(44), 31305–31311.CrossRefPubMed Neels, J. G., et al. (1999). The second and fourth cluster of class A cysteine-rich repeats of the low density lipoprotein receptor-related protein share ligand-binding properties. Journal of Biological Chemistry, 274(44), 31305–31311.CrossRefPubMed
go back to reference Parvathy, S., et al. (1999). Cleavage of Alzheimer’s amyloid precursor protein by alpha-secretase occurs at the surface of neuronal cells. Biochemistry, 38(30), 9728–9734.CrossRefPubMed Parvathy, S., et al. (1999). Cleavage of Alzheimer’s amyloid precursor protein by alpha-secretase occurs at the surface of neuronal cells. Biochemistry, 38(30), 9728–9734.CrossRefPubMed
go back to reference Pietrzik, C. U., et al. (2002). The cytoplasmic domain of the LDL receptor-related protein regulates multiple steps in APP processing. EMBO Journal, 21(21), 5691–5700.CrossRefPubMedPubMedCentral Pietrzik, C. U., et al. (2002). The cytoplasmic domain of the LDL receptor-related protein regulates multiple steps in APP processing. EMBO Journal, 21(21), 5691–5700.CrossRefPubMedPubMedCentral
go back to reference Pietrzik, C. U., et al. (2004). FE65 constitutes the functional link between the low-density lipoprotein receptor-related protein and the amyloid precursor protein. Journal of Neuroscience, 24(17), 4259–4265.CrossRefPubMed Pietrzik, C. U., et al. (2004). FE65 constitutes the functional link between the low-density lipoprotein receptor-related protein and the amyloid precursor protein. Journal of Neuroscience, 24(17), 4259–4265.CrossRefPubMed
go back to reference Qiu, Z., et al. (1999). Alpha2-macroglobulin enhances the clearance of endogenous soluble beta-amyloid peptide via low-density lipoprotein receptor-related protein in cortical neurons. Journal of Neurochemistry, 73(4), 1393–1398.CrossRefPubMed Qiu, Z., et al. (1999). Alpha2-macroglobulin enhances the clearance of endogenous soluble beta-amyloid peptide via low-density lipoprotein receptor-related protein in cortical neurons. Journal of Neurochemistry, 73(4), 1393–1398.CrossRefPubMed
go back to reference Rezai-Zadeh, K., et al. (2005). Green tea epigallocatechin-3-gallate (EGCG) modulates amyloid precursor protein cleavage and reduces cerebral amyloidosis in Alzheimer transgenic mice. Journal of Neuroscience, 25(38), 8807–8814.CrossRefPubMed Rezai-Zadeh, K., et al. (2005). Green tea epigallocatechin-3-gallate (EGCG) modulates amyloid precursor protein cleavage and reduces cerebral amyloidosis in Alzheimer transgenic mice. Journal of Neuroscience, 25(38), 8807–8814.CrossRefPubMed
go back to reference Sagare, A. P., et al. (2012). Low-density lipoprotein receptor-related protein 1: A physiological Abeta homeostatic mechanism with multiple therapeutic opportunities. Pharmacology & Therapeutics, 136(1), 94–105.CrossRef Sagare, A. P., et al. (2012). Low-density lipoprotein receptor-related protein 1: A physiological Abeta homeostatic mechanism with multiple therapeutic opportunities. Pharmacology & Therapeutics, 136(1), 94–105.CrossRef
go back to reference Shibata, M., et al. (2000). Clearance of Alzheimer’s amyloid-ss(1-40) peptide from brain by LDL receptor-related protein-1 at the blood-brain barrier. The Journal of Clinical Investigation, 106(12), 1489–1499.CrossRefPubMedPubMedCentral Shibata, M., et al. (2000). Clearance of Alzheimer’s amyloid-ss(1-40) peptide from brain by LDL receptor-related protein-1 at the blood-brain barrier. The Journal of Clinical Investigation, 106(12), 1489–1499.CrossRefPubMedPubMedCentral
go back to reference Silverberg, G. D., et al. (2010). Amyloid efflux transporter expression at the blood–brain barrier declines in normal aging. Journal of Neuropathology and Experimental Neurology, 69(10), 1034–1043.CrossRefPubMed Silverberg, G. D., et al. (2010). Amyloid efflux transporter expression at the blood–brain barrier declines in normal aging. Journal of Neuropathology and Experimental Neurology, 69(10), 1034–1043.CrossRefPubMed
go back to reference Ulery, P. G., et al. (2000). Modulation of beta-amyloid precursor protein processing by the low density lipoprotein receptor-related protein (LRP). Evidence that LRP contributes to the pathogenesis of Alzheimer’s disease. Journal of Biological Chemistry, 275(10), 7410–7415.CrossRefPubMed Ulery, P. G., et al. (2000). Modulation of beta-amyloid precursor protein processing by the low density lipoprotein receptor-related protein (LRP). Evidence that LRP contributes to the pathogenesis of Alzheimer’s disease. Journal of Biological Chemistry, 275(10), 7410–7415.CrossRefPubMed
go back to reference Vassar, R., et al. (1999). Beta-secretase cleavage of Alzheimer’s amyloid precursor protein by the transmembrane aspartic protease BACE. Science, 286(5440), 735–741.CrossRefPubMed Vassar, R., et al. (1999). Beta-secretase cleavage of Alzheimer’s amyloid precursor protein by the transmembrane aspartic protease BACE. Science, 286(5440), 735–741.CrossRefPubMed
go back to reference Waldron, E., et al. (2008). LRP1 modulates APP trafficking along early compartments of the secretory pathway. Neurobiology of Diseases, 31(2), 188–197.CrossRef Waldron, E., et al. (2008). LRP1 modulates APP trafficking along early compartments of the secretory pathway. Neurobiology of Diseases, 31(2), 188–197.CrossRef
go back to reference Zerbinatti, C. V., & Bu, G. (2005). LRP and Alzheimer’s disease. Reviews in the Neurosciences, 16(2), 123–135.CrossRefPubMed Zerbinatti, C. V., & Bu, G. (2005). LRP and Alzheimer’s disease. Reviews in the Neurosciences, 16(2), 123–135.CrossRefPubMed
go back to reference Zerbinatti, C. V., et al. (2004). Increased soluble amyloid-beta peptide and memory deficits in amyloid model mice overexpressing the low-density lipoprotein receptor-related protein. Proceedings of the National Academy of Sciences USA, 101(4), 1075–1080.CrossRef Zerbinatti, C. V., et al. (2004). Increased soluble amyloid-beta peptide and memory deficits in amyloid model mice overexpressing the low-density lipoprotein receptor-related protein. Proceedings of the National Academy of Sciences USA, 101(4), 1075–1080.CrossRef
go back to reference Zhang, X., & Song, W. (2013). The role of APP and BACE1 trafficking in APP processing and amyloid-beta generation. Alzheimer’s Research & Therapy, 5(5), 46.CrossRef Zhang, X., & Song, W. (2013). The role of APP and BACE1 trafficking in APP processing and amyloid-beta generation. Alzheimer’s Research & Therapy, 5(5), 46.CrossRef
go back to reference Zlokovic, B. V., et al. (2010). Low-density lipoprotein receptor-related protein-1: A serial clearance homeostatic mechanism controlling Alzheimer’s amyloid beta-peptide elimination from the brain. Journal of Neurochemistry, 115(5), 1077–1089.CrossRefPubMedPubMedCentral Zlokovic, B. V., et al. (2010). Low-density lipoprotein receptor-related protein-1: A serial clearance homeostatic mechanism controlling Alzheimer’s amyloid beta-peptide elimination from the brain. Journal of Neurochemistry, 115(5), 1077–1089.CrossRefPubMedPubMedCentral
Metadata
Title
Low-Density Lipoprotein Receptor-Related Protein-1 (LRP1) C4408R Mutant Promotes Amyloid Precursor Protein (APP) α-Cleavage in Vitro
Authors
Huayan Hou
Ahsan Habib
Dan Zi
Kathy Tian
Jun Tian
Brian Giunta
Darrell Sawmiller
Jun Tan
Publication date
01-09-2017
Publisher
Springer US
Published in
NeuroMolecular Medicine / Issue 2-3/2017
Print ISSN: 1535-1084
Electronic ISSN: 1559-1174
DOI
https://doi.org/10.1007/s12017-017-8446-x

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