Cerebral Apolipoprotein D Exits the Brain and Accumulates in Peripheral Tissues

Apolipoprotein D (ApoD) is a secreted lipocalin associated with neuroprotection and lipid metabolism. In rodent, the bulk of its expression occurs in the central nervous system. Despite this, ApoD has profound effects in peripheral tissues, indicating that neural ApoD may reach peripheral organs. We...

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Main Authors: Frederik Desmarais, Vincent Hervé, Karl F. Bergeron, Gaétan Ravaut, Morgane Perrotte, Guillaume Fyfe-Desmarais, Eric Rassart, Charles Ramassamy, Catherine Mounier
Format: Article
Language:English
Published: MDPI AG 2021-04-01
Series:International Journal of Molecular Sciences
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Online Access:https://www.mdpi.com/1422-0067/22/8/4118
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spelling doaj-6666592feaa74dc0b91334e162e2b1c92021-04-16T23:01:21ZengMDPI AGInternational Journal of Molecular Sciences1661-65961422-00672021-04-01224118411810.3390/ijms22084118Cerebral Apolipoprotein D Exits the Brain and Accumulates in Peripheral TissuesFrederik Desmarais0Vincent Hervé1Karl F. Bergeron2Gaétan Ravaut3Morgane Perrotte4Guillaume Fyfe-Desmarais5Eric Rassart6Charles Ramassamy7Catherine Mounier8Laboratoire du Métabolisme Moléculaire des Lipides, Centre de Recherches CERMO-FC, Département des Sciences Biologiques, Université du Québec à Montréal (UQAM), 141 av. du Président-Kennedy, Montréal, QC H2X 1Y4, CanadaLaboratoire de Biologie Moléculaire, Département des Sciences Biologiques, Université du Québec à Montréal (UQAM), 141 av. du Président-Kennedy, Montréal, QC H2X 1Y4, CanadaLaboratoire du Métabolisme Moléculaire des Lipides, Centre de Recherches CERMO-FC, Département des Sciences Biologiques, Université du Québec à Montréal (UQAM), 141 av. du Président-Kennedy, Montréal, QC H2X 1Y4, CanadaLaboratoire du Métabolisme Moléculaire des Lipides, Centre de Recherches CERMO-FC, Département des Sciences Biologiques, Université du Québec à Montréal (UQAM), 141 av. du Président-Kennedy, Montréal, QC H2X 1Y4, CanadaCentre Armand-Frappier Santé Biotechnologie, Institut National de la Recherche Scientifique (INRS), 531 boul. des Prairies, Laval, QC H7V 1B7, CanadaLaboratoire du Métabolisme Moléculaire des Lipides, Centre de Recherches CERMO-FC, Département des Sciences Biologiques, Université du Québec à Montréal (UQAM), 141 av. du Président-Kennedy, Montréal, QC H2X 1Y4, CanadaLaboratoire de Biologie Moléculaire, Département des Sciences Biologiques, Université du Québec à Montréal (UQAM), 141 av. du Président-Kennedy, Montréal, QC H2X 1Y4, CanadaCentre Armand-Frappier Santé Biotechnologie, Institut National de la Recherche Scientifique (INRS), 531 boul. des Prairies, Laval, QC H7V 1B7, CanadaLaboratoire du Métabolisme Moléculaire des Lipides, Centre de Recherches CERMO-FC, Département des Sciences Biologiques, Université du Québec à Montréal (UQAM), 141 av. du Président-Kennedy, Montréal, QC H2X 1Y4, CanadaApolipoprotein D (ApoD) is a secreted lipocalin associated with neuroprotection and lipid metabolism. In rodent, the bulk of its expression occurs in the central nervous system. Despite this, ApoD has profound effects in peripheral tissues, indicating that neural ApoD may reach peripheral organs. We endeavor to determine if cerebral ApoD can reach the circulation and accumulate in peripheral tissues. Three hours was necessary for over 40% of all the radiolabeled human ApoD (hApoD), injected bilaterally, to exit the central nervous system (CNS). Once in circulation, hApoD accumulates mostly in the kidneys/urine, liver, and muscles. Accumulation specificity of hApoD in these tissues was strongly correlated with the expression of lowly glycosylated basigin (BSG, CD147). hApoD was observed to pass through bEnd.3 blood brain barrier endothelial cells monolayers. However, cyclophilin A did not impact hApoD internalization rates in bEnd.3, indicating that ApoD exit from the brain is either independent of BSG or relies on additional cell types. Overall, our data showed that ApoD can quickly and efficiently exit the CNS and reach the liver and kidneys/urine, organs linked to the recycling and excretion of lipids and toxins. This indicated that cerebral overexpression during neurodegenerative episodes may serve to evacuate neurotoxic ApoD ligands from the CNS.https://www.mdpi.com/1422-0067/22/8/4118apolipoprotein Dbasiginprotein accumulationblood-brain barrier
collection DOAJ
language English
format Article
sources DOAJ
author Frederik Desmarais
Vincent Hervé
Karl F. Bergeron
Gaétan Ravaut
Morgane Perrotte
Guillaume Fyfe-Desmarais
Eric Rassart
Charles Ramassamy
Catherine Mounier
spellingShingle Frederik Desmarais
Vincent Hervé
Karl F. Bergeron
Gaétan Ravaut
Morgane Perrotte
Guillaume Fyfe-Desmarais
Eric Rassart
Charles Ramassamy
Catherine Mounier
Cerebral Apolipoprotein D Exits the Brain and Accumulates in Peripheral Tissues
International Journal of Molecular Sciences
apolipoprotein D
basigin
protein accumulation
blood-brain barrier
author_facet Frederik Desmarais
Vincent Hervé
Karl F. Bergeron
Gaétan Ravaut
Morgane Perrotte
Guillaume Fyfe-Desmarais
Eric Rassart
Charles Ramassamy
Catherine Mounier
author_sort Frederik Desmarais
title Cerebral Apolipoprotein D Exits the Brain and Accumulates in Peripheral Tissues
title_short Cerebral Apolipoprotein D Exits the Brain and Accumulates in Peripheral Tissues
title_full Cerebral Apolipoprotein D Exits the Brain and Accumulates in Peripheral Tissues
title_fullStr Cerebral Apolipoprotein D Exits the Brain and Accumulates in Peripheral Tissues
title_full_unstemmed Cerebral Apolipoprotein D Exits the Brain and Accumulates in Peripheral Tissues
title_sort cerebral apolipoprotein d exits the brain and accumulates in peripheral tissues
publisher MDPI AG
series International Journal of Molecular Sciences
issn 1661-6596
1422-0067
publishDate 2021-04-01
description Apolipoprotein D (ApoD) is a secreted lipocalin associated with neuroprotection and lipid metabolism. In rodent, the bulk of its expression occurs in the central nervous system. Despite this, ApoD has profound effects in peripheral tissues, indicating that neural ApoD may reach peripheral organs. We endeavor to determine if cerebral ApoD can reach the circulation and accumulate in peripheral tissues. Three hours was necessary for over 40% of all the radiolabeled human ApoD (hApoD), injected bilaterally, to exit the central nervous system (CNS). Once in circulation, hApoD accumulates mostly in the kidneys/urine, liver, and muscles. Accumulation specificity of hApoD in these tissues was strongly correlated with the expression of lowly glycosylated basigin (BSG, CD147). hApoD was observed to pass through bEnd.3 blood brain barrier endothelial cells monolayers. However, cyclophilin A did not impact hApoD internalization rates in bEnd.3, indicating that ApoD exit from the brain is either independent of BSG or relies on additional cell types. Overall, our data showed that ApoD can quickly and efficiently exit the CNS and reach the liver and kidneys/urine, organs linked to the recycling and excretion of lipids and toxins. This indicated that cerebral overexpression during neurodegenerative episodes may serve to evacuate neurotoxic ApoD ligands from the CNS.
topic apolipoprotein D
basigin
protein accumulation
blood-brain barrier
url https://www.mdpi.com/1422-0067/22/8/4118
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