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β-amyloid Peptide Binds and Regulates Ectopic ATP Synthase α-Chain on Neural Surface
ABSTRACT Accumulation of the amyloid β protein (Aβ) in the brain is an important step in the pathogenesis of Alzheimer's disease. Many molecules could bind with Aβ, among which some molecules mediate Aβ neuronal toxicity. Thus, it is of interest to study the binding proteins of Aβ, and the func...
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Published in: | International journal of neuroscience 2012-06, Vol.122 (6), p.290-297 |
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container_title | International journal of neuroscience |
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creator | Xing, San-Li Chen, Bo Shen, Ding-Zhu Zhu, Cui-Qing |
description | ABSTRACT
Accumulation of the amyloid β protein (Aβ) in the brain is an important step in the pathogenesis of Alzheimer's disease. Many molecules could bind with Aβ, among which some molecules mediate Aβ neuronal toxicity. Thus, it is of interest to study the binding proteins of Aβ, and the functions that might be affected by Aβ. In the present study, we observed that accumulation of α-subunit of ATP synthase is associated with aggregates of Aβ proteins in amyloid plaques of amyloid precursor protein/presennillin-1 transgenic mice, and identified the α-subunit of ATP synthase as one of the Aβ binding proteins on the plasma membrane of neural cells by Western blot and mass spectrometry. In order to evaluate the consequences of the interaction between Aβ and surface α-subunit of ATP synthase, the extracellular ATP generation was analyzed, which showed that aggregated Aβ partially inhibited the extracellular generation of ATP, but was unable to significantly induce a decrease in cell surface ATP synthase α on neurons. These results suggest that the cell surface ATP synthase α is a binding protein for Aβ on neural cells, the functional inhibition of surface ATP synthase might be involved in machinery of brain malfunction in Aβ-mediated pathogenesis of Alzheimer's disease. |
doi_str_mv | 10.3109/00207454.2011.649867 |
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Accumulation of the amyloid β protein (Aβ) in the brain is an important step in the pathogenesis of Alzheimer's disease. Many molecules could bind with Aβ, among which some molecules mediate Aβ neuronal toxicity. Thus, it is of interest to study the binding proteins of Aβ, and the functions that might be affected by Aβ. In the present study, we observed that accumulation of α-subunit of ATP synthase is associated with aggregates of Aβ proteins in amyloid plaques of amyloid precursor protein/presennillin-1 transgenic mice, and identified the α-subunit of ATP synthase as one of the Aβ binding proteins on the plasma membrane of neural cells by Western blot and mass spectrometry. In order to evaluate the consequences of the interaction between Aβ and surface α-subunit of ATP synthase, the extracellular ATP generation was analyzed, which showed that aggregated Aβ partially inhibited the extracellular generation of ATP, but was unable to significantly induce a decrease in cell surface ATP synthase α on neurons. These results suggest that the cell surface ATP synthase α is a binding protein for Aβ on neural cells, the functional inhibition of surface ATP synthase might be involved in machinery of brain malfunction in Aβ-mediated pathogenesis of Alzheimer's disease.</description><identifier>ISSN: 0020-7454</identifier><identifier>EISSN: 1563-5279</identifier><identifier>EISSN: 1543-5245</identifier><identifier>DOI: 10.3109/00207454.2011.649867</identifier><identifier>PMID: 22185089</identifier><language>eng</language><publisher>England: Informa Healthcare</publisher><subject>Adenosine Triphosphate - biosynthesis ; aggregated Aβ ; Alzheimer's disease ; Amyloid beta-Peptides - metabolism ; Amyloid beta-Protein Precursor - genetics ; Animals ; ATP production ; ATP synthase α ; Brain - metabolism ; Brain - ultrastructure ; Cells, Cultured ; Female ; Male ; Mice ; Mice, Transgenic ; Mitochondrial Proton-Translocating ATPases - metabolism ; Neurons - metabolism ; Neurons - ultrastructure ; Peptide Fragments - metabolism ; Plaque, Amyloid - metabolism ; Presenilin-1 - genetics ; Rats ; Rats, Sprague-Dawley</subject><ispartof>International journal of neuroscience, 2012-06, Vol.122 (6), p.290-297</ispartof><rights>2012 Informa Healthcare USA, Inc. 2012</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c418t-7b4755d380e5d44c1785b686ad93bed207be61aedf518491223a2dc0999304623</citedby><cites>FETCH-LOGICAL-c418t-7b4755d380e5d44c1785b686ad93bed207be61aedf518491223a2dc0999304623</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27922,27923</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22185089$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Xing, San-Li</creatorcontrib><creatorcontrib>Chen, Bo</creatorcontrib><creatorcontrib>Shen, Ding-Zhu</creatorcontrib><creatorcontrib>Zhu, Cui-Qing</creatorcontrib><title>β-amyloid Peptide Binds and Regulates Ectopic ATP Synthase α-Chain on Neural Surface</title><title>International journal of neuroscience</title><addtitle>Int J Neurosci</addtitle><description>ABSTRACT
Accumulation of the amyloid β protein (Aβ) in the brain is an important step in the pathogenesis of Alzheimer's disease. Many molecules could bind with Aβ, among which some molecules mediate Aβ neuronal toxicity. Thus, it is of interest to study the binding proteins of Aβ, and the functions that might be affected by Aβ. In the present study, we observed that accumulation of α-subunit of ATP synthase is associated with aggregates of Aβ proteins in amyloid plaques of amyloid precursor protein/presennillin-1 transgenic mice, and identified the α-subunit of ATP synthase as one of the Aβ binding proteins on the plasma membrane of neural cells by Western blot and mass spectrometry. In order to evaluate the consequences of the interaction between Aβ and surface α-subunit of ATP synthase, the extracellular ATP generation was analyzed, which showed that aggregated Aβ partially inhibited the extracellular generation of ATP, but was unable to significantly induce a decrease in cell surface ATP synthase α on neurons. These results suggest that the cell surface ATP synthase α is a binding protein for Aβ on neural cells, the functional inhibition of surface ATP synthase might be involved in machinery of brain malfunction in Aβ-mediated pathogenesis of Alzheimer's disease.</description><subject>Adenosine Triphosphate - biosynthesis</subject><subject>aggregated Aβ</subject><subject>Alzheimer's disease</subject><subject>Amyloid beta-Peptides - metabolism</subject><subject>Amyloid beta-Protein Precursor - genetics</subject><subject>Animals</subject><subject>ATP production</subject><subject>ATP synthase α</subject><subject>Brain - metabolism</subject><subject>Brain - ultrastructure</subject><subject>Cells, Cultured</subject><subject>Female</subject><subject>Male</subject><subject>Mice</subject><subject>Mice, Transgenic</subject><subject>Mitochondrial Proton-Translocating ATPases - metabolism</subject><subject>Neurons - metabolism</subject><subject>Neurons - ultrastructure</subject><subject>Peptide Fragments - metabolism</subject><subject>Plaque, Amyloid - metabolism</subject><subject>Presenilin-1 - genetics</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><issn>0020-7454</issn><issn>1563-5279</issn><issn>1543-5245</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><recordid>eNp9kO1KwzAUhoMoOqZ3IJIb6EzSpE3-KHPMDxg6_PpbTpPURbp2JC2yy9IL2TXZMhX8s1_hwPO-J-dB6JSSUUyJOieEkZQLPmKE0lHClUzSPTSgIokjwVK1jwY9EvXMEToJweXdHCvFpDxER4xRKYhUA_S6-YpguS5rZ_DcrhpnLL5ylQkYKoMf7VtbQmMDnuqmXjmNx89z_LSumgUEizef0WQBrsJ1he9t66HET60vQNtjdFBAGezJzztEL9fT58ltNHu4uZuMZ5HmVDZRmvNUCBNLYoXhXNNUijyRCRgV59Z0N-Y2oWBNIajkijIWAzOaKKViwhMWDxHf9mpfh-Btka28W4JfZ5Rkvans11TWm8q2prrY2Ta2avOlNX-hXy8dcLkFXFXUfgkftS9N1kAnyhceKu1CX79zxcW_hoWFsllo8DZ7r1tfdVZ2__EbL4CK6Q</recordid><startdate>20120601</startdate><enddate>20120601</enddate><creator>Xing, San-Li</creator><creator>Chen, Bo</creator><creator>Shen, Ding-Zhu</creator><creator>Zhu, Cui-Qing</creator><general>Informa Healthcare</general><general>Taylor & Francis</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20120601</creationdate><title>β-amyloid Peptide Binds and Regulates Ectopic ATP Synthase α-Chain on Neural Surface</title><author>Xing, San-Li ; Chen, Bo ; Shen, Ding-Zhu ; Zhu, Cui-Qing</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c418t-7b4755d380e5d44c1785b686ad93bed207be61aedf518491223a2dc0999304623</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Adenosine Triphosphate - biosynthesis</topic><topic>aggregated Aβ</topic><topic>Alzheimer's disease</topic><topic>Amyloid beta-Peptides - metabolism</topic><topic>Amyloid beta-Protein Precursor - genetics</topic><topic>Animals</topic><topic>ATP production</topic><topic>ATP synthase α</topic><topic>Brain - metabolism</topic><topic>Brain - ultrastructure</topic><topic>Cells, Cultured</topic><topic>Female</topic><topic>Male</topic><topic>Mice</topic><topic>Mice, Transgenic</topic><topic>Mitochondrial Proton-Translocating ATPases - metabolism</topic><topic>Neurons - metabolism</topic><topic>Neurons - ultrastructure</topic><topic>Peptide Fragments - metabolism</topic><topic>Plaque, Amyloid - metabolism</topic><topic>Presenilin-1 - genetics</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Xing, San-Li</creatorcontrib><creatorcontrib>Chen, Bo</creatorcontrib><creatorcontrib>Shen, Ding-Zhu</creatorcontrib><creatorcontrib>Zhu, Cui-Qing</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>International journal of neuroscience</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Xing, San-Li</au><au>Chen, Bo</au><au>Shen, Ding-Zhu</au><au>Zhu, Cui-Qing</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>β-amyloid Peptide Binds and Regulates Ectopic ATP Synthase α-Chain on Neural Surface</atitle><jtitle>International journal of neuroscience</jtitle><addtitle>Int J Neurosci</addtitle><date>2012-06-01</date><risdate>2012</risdate><volume>122</volume><issue>6</issue><spage>290</spage><epage>297</epage><pages>290-297</pages><issn>0020-7454</issn><eissn>1563-5279</eissn><eissn>1543-5245</eissn><abstract>ABSTRACT
Accumulation of the amyloid β protein (Aβ) in the brain is an important step in the pathogenesis of Alzheimer's disease. Many molecules could bind with Aβ, among which some molecules mediate Aβ neuronal toxicity. Thus, it is of interest to study the binding proteins of Aβ, and the functions that might be affected by Aβ. In the present study, we observed that accumulation of α-subunit of ATP synthase is associated with aggregates of Aβ proteins in amyloid plaques of amyloid precursor protein/presennillin-1 transgenic mice, and identified the α-subunit of ATP synthase as one of the Aβ binding proteins on the plasma membrane of neural cells by Western blot and mass spectrometry. In order to evaluate the consequences of the interaction between Aβ and surface α-subunit of ATP synthase, the extracellular ATP generation was analyzed, which showed that aggregated Aβ partially inhibited the extracellular generation of ATP, but was unable to significantly induce a decrease in cell surface ATP synthase α on neurons. These results suggest that the cell surface ATP synthase α is a binding protein for Aβ on neural cells, the functional inhibition of surface ATP synthase might be involved in machinery of brain malfunction in Aβ-mediated pathogenesis of Alzheimer's disease.</abstract><cop>England</cop><pub>Informa Healthcare</pub><pmid>22185089</pmid><doi>10.3109/00207454.2011.649867</doi><tpages>8</tpages></addata></record> |
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source | Taylor and Francis:Jisc Collections:Taylor and Francis Read and Publish Agreement 2024-2025:Medical Collection (Reading list) |
subjects | Adenosine Triphosphate - biosynthesis aggregated Aβ Alzheimer's disease Amyloid beta-Peptides - metabolism Amyloid beta-Protein Precursor - genetics Animals ATP production ATP synthase α Brain - metabolism Brain - ultrastructure Cells, Cultured Female Male Mice Mice, Transgenic Mitochondrial Proton-Translocating ATPases - metabolism Neurons - metabolism Neurons - ultrastructure Peptide Fragments - metabolism Plaque, Amyloid - metabolism Presenilin-1 - genetics Rats Rats, Sprague-Dawley |
title | β-amyloid Peptide Binds and Regulates Ectopic ATP Synthase α-Chain on Neural Surface |
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