A Heme Oxygenase-1 Transducer Model of Degenerative and Developmental Brain Disorders
Identifieur interne : 001A94 ( Ncbi/Merge ); précédent : 001A93; suivant : 001A95A Heme Oxygenase-1 Transducer Model of Degenerative and Developmental Brain Disorders
Auteurs : Hyman M. Schipper [Canada] ; Wei SongSource :
- International Journal of Molecular Sciences [ 1422-0067 ] ; 2015.
English descriptors
- KwdEn :
- MESH :
- chemical , genetics : Heme Oxygenase-1.
- genetics : Alzheimer Disease, Parkinson Disease.
- metabolism : Alzheimer Disease, Heme Oxygenase-1, Iron, Parkinson Disease.
- therapy : Alzheimer Disease, Parkinson Disease.
- Animals, Humans, Signal Transduction.
Abstract
Heme oxygenase-1 (HO-1) is a 32 kDa protein which catalyzes the breakdown of heme to free iron, carbon monoxide and biliverdin. The
Url:
DOI: 10.3390/ijms16035400
PubMed: 25761244
PubMed Central: 4394483
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PMC:4394483Le document en format XML
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<sourceDesc><biblStruct><analytic><title xml:lang="en" level="a" type="main">A Heme Oxygenase-1 Transducer Model of Degenerative and Developmental Brain Disorders</title>
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<author><name sortKey="Song, Wei" sort="Song, Wei" uniqKey="Song W" first="Wei" last="Song">Wei Song</name>
<affiliation><nlm:aff id="af1-ijms-16-05400">Bloomfield Centre for Research in Aging, Lady Davis Institute for Medical Research, Jewish General Hospital, Montreal, QC H3T1E2, Canada; E-Mail:<email>wsong39@yahoo.com</email>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Alzheimer Disease (genetics)</term>
<term>Alzheimer Disease (metabolism)</term>
<term>Alzheimer Disease (therapy)</term>
<term>Animals</term>
<term>Heme Oxygenase-1 (genetics)</term>
<term>Heme Oxygenase-1 (metabolism)</term>
<term>Humans</term>
<term>Iron (metabolism)</term>
<term>Parkinson Disease (genetics)</term>
<term>Parkinson Disease (metabolism)</term>
<term>Parkinson Disease (therapy)</term>
<term>Signal Transduction</term>
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<keywords scheme="MESH" type="chemical" qualifier="genetics" xml:lang="en"><term>Heme Oxygenase-1</term>
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<keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Alzheimer Disease</term>
<term>Parkinson Disease</term>
</keywords>
<keywords scheme="MESH" qualifier="metabolism" xml:lang="en"><term>Alzheimer Disease</term>
<term>Heme Oxygenase-1</term>
<term>Iron</term>
<term>Parkinson Disease</term>
</keywords>
<keywords scheme="MESH" qualifier="therapy" xml:lang="en"><term>Alzheimer Disease</term>
<term>Parkinson Disease</term>
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<keywords scheme="MESH" xml:lang="en"><term>Animals</term>
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<front><div type="abstract" xml:lang="en"><p>Heme oxygenase-1 (HO-1) is a 32 kDa protein which catalyzes the breakdown of heme to free iron, carbon monoxide and biliverdin. The <italic>Hmox1</italic>
promoter contains numerous consensus sequences that render the gene exquisitely sensitive to induction by diverse pro-oxidant and inflammatory stimuli. In “stressed” astroglia, HO-1 hyperactivity promotes mitochondrial iron sequestration and macroautophagy and may thereby contribute to the pathological iron deposition and bioenergetic failure documented in Alzheimer disease, Parkinson disease and certain neurodevelopmental conditions. Glial HO-1 expression may also impact neuroplasticity and cell survival by modulating brain sterol metabolism and the proteasomal degradation of neurotoxic proteins. The glial HO-1 response may represent a pivotal transducer of noxious environmental and endogenous stressors into patterns of neural damage and repair characteristic of many human degenerative and developmental CNS disorders.</p>
</div>
</front>
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<double pmid="25761244"><pmc><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">A Heme Oxygenase-1 Transducer Model of Degenerative and Developmental Brain Disorders</title>
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<affiliation><nlm:aff id="af1-ijms-16-05400">Bloomfield Centre for Research in Aging, Lady Davis Institute for Medical Research, Jewish General Hospital, Montreal, QC H3T1E2, Canada; E-Mail:<email>wsong39@yahoo.com</email>
</nlm:aff>
</affiliation>
<affiliation wicri:level="1"><nlm:aff id="af2-ijms-16-05400">Department of Neurology & Neurosurgery and Department of Medicine, McGill University and Jewish General Hospital, Montreal, QC H3T1E2, Canada</nlm:aff>
<country xml:lang="fr">Canada</country>
<wicri:regionArea>Department of Neurology & Neurosurgery and Department of Medicine, McGill University and Jewish General Hospital, Montreal, QC H3T1E2</wicri:regionArea>
<wicri:noRegion>QC H3T1E2</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Song, Wei" sort="Song, Wei" uniqKey="Song W" first="Wei" last="Song">Wei Song</name>
<affiliation><nlm:aff id="af1-ijms-16-05400">Bloomfield Centre for Research in Aging, Lady Davis Institute for Medical Research, Jewish General Hospital, Montreal, QC H3T1E2, Canada; E-Mail:<email>wsong39@yahoo.com</email>
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<idno type="RBID">PMC:4394483</idno>
<idno type="doi">10.3390/ijms16035400</idno>
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<sourceDesc><biblStruct><analytic><title xml:lang="en" level="a" type="main">A Heme Oxygenase-1 Transducer Model of Degenerative and Developmental Brain Disorders</title>
<author><name sortKey="Schipper, Hyman M" sort="Schipper, Hyman M" uniqKey="Schipper H" first="Hyman M." last="Schipper">Hyman M. Schipper</name>
<affiliation><nlm:aff id="af1-ijms-16-05400">Bloomfield Centre for Research in Aging, Lady Davis Institute for Medical Research, Jewish General Hospital, Montreal, QC H3T1E2, Canada; E-Mail:<email>wsong39@yahoo.com</email>
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</affiliation>
<affiliation wicri:level="1"><nlm:aff id="af2-ijms-16-05400">Department of Neurology & Neurosurgery and Department of Medicine, McGill University and Jewish General Hospital, Montreal, QC H3T1E2, Canada</nlm:aff>
<country xml:lang="fr">Canada</country>
<wicri:regionArea>Department of Neurology & Neurosurgery and Department of Medicine, McGill University and Jewish General Hospital, Montreal, QC H3T1E2</wicri:regionArea>
<wicri:noRegion>QC H3T1E2</wicri:noRegion>
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<author><name sortKey="Song, Wei" sort="Song, Wei" uniqKey="Song W" first="Wei" last="Song">Wei Song</name>
<affiliation><nlm:aff id="af1-ijms-16-05400">Bloomfield Centre for Research in Aging, Lady Davis Institute for Medical Research, Jewish General Hospital, Montreal, QC H3T1E2, Canada; E-Mail:<email>wsong39@yahoo.com</email>
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<series><title level="j">International Journal of Molecular Sciences</title>
<idno type="eISSN">1422-0067</idno>
<imprint><date when="2015">2015</date>
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<front><div type="abstract" xml:lang="en"><p>Heme oxygenase-1 (HO-1) is a 32 kDa protein which catalyzes the breakdown of heme to free iron, carbon monoxide and biliverdin. The <italic>Hmox1</italic>
promoter contains numerous consensus sequences that render the gene exquisitely sensitive to induction by diverse pro-oxidant and inflammatory stimuli. In “stressed” astroglia, HO-1 hyperactivity promotes mitochondrial iron sequestration and macroautophagy and may thereby contribute to the pathological iron deposition and bioenergetic failure documented in Alzheimer disease, Parkinson disease and certain neurodevelopmental conditions. Glial HO-1 expression may also impact neuroplasticity and cell survival by modulating brain sterol metabolism and the proteasomal degradation of neurotoxic proteins. The glial HO-1 response may represent a pivotal transducer of noxious environmental and endogenous stressors into patterns of neural damage and repair characteristic of many human degenerative and developmental CNS disorders.</p>
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</pmc>
<pubmed><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">A heme oxygenase-1 transducer model of degenerative and developmental brain disorders.</title>
<author><name sortKey="Schipper, Hyman M" sort="Schipper, Hyman M" uniqKey="Schipper H" first="Hyman M" last="Schipper">Hyman M. Schipper</name>
<affiliation wicri:level="1"><nlm:affiliation>Bloomfield Centre for Research in Aging, Lady Davis Institute for Medical Research, Jewish General Hospital, Montreal, QC H3T1E2, Canada. hyman.schipper@mcgill.ca.</nlm:affiliation>
<country xml:lang="fr">Canada</country>
<wicri:regionArea>Bloomfield Centre for Research in Aging, Lady Davis Institute for Medical Research, Jewish General Hospital, Montreal, QC H3T1E2</wicri:regionArea>
<wicri:noRegion>QC H3T1E2</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Song, Wei" sort="Song, Wei" uniqKey="Song W" first="Wei" last="Song">Wei Song</name>
<affiliation wicri:level="1"><nlm:affiliation>Bloomfield Centre for Research in Aging, Lady Davis Institute for Medical Research, Jewish General Hospital, Montreal, QC H3T1E2, Canada. wsong39@yahoo.com.</nlm:affiliation>
<country xml:lang="fr">Canada</country>
<wicri:regionArea>Bloomfield Centre for Research in Aging, Lady Davis Institute for Medical Research, Jewish General Hospital, Montreal, QC H3T1E2</wicri:regionArea>
<wicri:noRegion>QC H3T1E2</wicri:noRegion>
</affiliation>
</author>
</titleStmt>
<publicationStmt><idno type="wicri:source">PubMed</idno>
<date when="2015">2015</date>
<idno type="RBID">pubmed:25761244</idno>
<idno type="pmid">25761244</idno>
<idno type="doi">10.3390/ijms16035400</idno>
<idno type="wicri:Area/PubMed/Corpus">000542</idno>
<idno type="wicri:explorRef" wicri:stream="PubMed" wicri:step="Corpus" wicri:corpus="PubMed">000542</idno>
<idno type="wicri:Area/PubMed/Curation">000542</idno>
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<idno type="wicri:Area/PubMed/Checkpoint">000542</idno>
<idno type="wicri:explorRef" wicri:stream="Checkpoint" wicri:step="PubMed">000542</idno>
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<sourceDesc><biblStruct><analytic><title xml:lang="en">A heme oxygenase-1 transducer model of degenerative and developmental brain disorders.</title>
<author><name sortKey="Schipper, Hyman M" sort="Schipper, Hyman M" uniqKey="Schipper H" first="Hyman M" last="Schipper">Hyman M. Schipper</name>
<affiliation wicri:level="1"><nlm:affiliation>Bloomfield Centre for Research in Aging, Lady Davis Institute for Medical Research, Jewish General Hospital, Montreal, QC H3T1E2, Canada. hyman.schipper@mcgill.ca.</nlm:affiliation>
<country xml:lang="fr">Canada</country>
<wicri:regionArea>Bloomfield Centre for Research in Aging, Lady Davis Institute for Medical Research, Jewish General Hospital, Montreal, QC H3T1E2</wicri:regionArea>
<wicri:noRegion>QC H3T1E2</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Song, Wei" sort="Song, Wei" uniqKey="Song W" first="Wei" last="Song">Wei Song</name>
<affiliation wicri:level="1"><nlm:affiliation>Bloomfield Centre for Research in Aging, Lady Davis Institute for Medical Research, Jewish General Hospital, Montreal, QC H3T1E2, Canada. wsong39@yahoo.com.</nlm:affiliation>
<country xml:lang="fr">Canada</country>
<wicri:regionArea>Bloomfield Centre for Research in Aging, Lady Davis Institute for Medical Research, Jewish General Hospital, Montreal, QC H3T1E2</wicri:regionArea>
<wicri:noRegion>QC H3T1E2</wicri:noRegion>
</affiliation>
</author>
</analytic>
<series><title level="j">International journal of molecular sciences</title>
<idno type="eISSN">1422-0067</idno>
<imprint><date when="2015" type="published">2015</date>
</imprint>
</series>
</biblStruct>
</sourceDesc>
</fileDesc>
<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Alzheimer Disease (genetics)</term>
<term>Alzheimer Disease (metabolism)</term>
<term>Alzheimer Disease (therapy)</term>
<term>Animals</term>
<term>Heme Oxygenase-1 (genetics)</term>
<term>Heme Oxygenase-1 (metabolism)</term>
<term>Humans</term>
<term>Iron (metabolism)</term>
<term>Parkinson Disease (genetics)</term>
<term>Parkinson Disease (metabolism)</term>
<term>Parkinson Disease (therapy)</term>
<term>Signal Transduction</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="genetics" xml:lang="en"><term>Heme Oxygenase-1</term>
</keywords>
<keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Alzheimer Disease</term>
<term>Parkinson Disease</term>
</keywords>
<keywords scheme="MESH" qualifier="metabolism" xml:lang="en"><term>Alzheimer Disease</term>
<term>Heme Oxygenase-1</term>
<term>Iron</term>
<term>Parkinson Disease</term>
</keywords>
<keywords scheme="MESH" qualifier="therapy" xml:lang="en"><term>Alzheimer Disease</term>
<term>Parkinson Disease</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Animals</term>
<term>Humans</term>
<term>Signal Transduction</term>
</keywords>
</textClass>
</profileDesc>
</teiHeader>
<front><div type="abstract" xml:lang="en">Heme oxygenase-1 (HO-1) is a 32 kDa protein which catalyzes the breakdown of heme to free iron, carbon monoxide and biliverdin. The Hmox1 promoter contains numerous consensus sequences that render the gene exquisitely sensitive to induction by diverse pro-oxidant and inflammatory stimuli. In "stressed" astroglia, HO-1 hyperactivity promotes mitochondrial iron sequestration and macroautophagy and may thereby contribute to the pathological iron deposition and bioenergetic failure documented in Alzheimer disease, Parkinson disease and certain neurodevelopmental conditions. Glial HO-1 expression may also impact neuroplasticity and cell survival by modulating brain sterol metabolism and the proteasomal degradation of neurotoxic proteins. The glial HO-1 response may represent a pivotal transducer of noxious environmental and endogenous stressors into patterns of neural damage and repair characteristic of many human degenerative and developmental CNS disorders.</div>
</front>
</TEI>
</pubmed>
</double>
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