Vascular basement membranes as pathways for the passage of fluid into and out of the brain
In the absence of conventional lymphatics, drainage of interstitial fluid and solutes from the brain parenchyma to cervical lymph nodes is along basement membranes in the walls of cerebral capillaries and tunica media of arteries. Perivascular pathways are also involved in the entry of CSF into the...
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description | In the absence of conventional lymphatics, drainage of interstitial fluid and solutes from the brain parenchyma to cervical lymph nodes is along basement membranes in the walls of cerebral capillaries and tunica media of arteries. Perivascular pathways are also involved in the entry of CSF into the brain by the convective influx/glymphatic system. The objective of this study is to differentiate the cerebral vascular basement membrane pathways by which fluid passes out of the brain from the pathway by which CSF enters the brain. Experiment 1: 0.5 µl of soluble biotinylated or fluorescent Aβ, or 1 µl 15 nm gold nanoparticles was injected into the mouse hippocampus and their distributions determined at 5 min by transmission electron microscopy. Aβ was distributed within the extracellular spaces of the hippocampus and within basement membranes of capillaries and tunica media of arteries. Nanoparticles did not enter capillary basement membranes from the extracellular spaces. Experiment 2: 2 µl of 15 nm nanoparticles were injected into mouse CSF. Within 5min, groups of nanoparticles were present in the pial-glial basement membrane on the outer aspect of cortical arteries between the investing layer of pia mater and the glia limitans. The results of this study and previous research suggest that cerebral vascular basement membranes form the pathways by which fluid passes into and out of the brain but that different basement membrane layers are involved. The significance of these findings for neuroimmunology, Alzheimer’s disease, drug delivery to the brain and the concept of the Virchow–Robin space are discussed. |
doi_str_mv | 10.1007/s00401-016-1555-z |
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J. ; Sharp, Matthew MacGregor ; Albargothy, Nazira J. ; Fernandes, Rute ; Hawkes, Cheryl A. ; Verma, Ajay ; Weller, Roy O. ; Carare, Roxana O.</creator><creatorcontrib>Morris, Alan W. J. ; Sharp, Matthew MacGregor ; Albargothy, Nazira J. ; Fernandes, Rute ; Hawkes, Cheryl A. ; Verma, Ajay ; Weller, Roy O. ; Carare, Roxana O.</creatorcontrib><description>In the absence of conventional lymphatics, drainage of interstitial fluid and solutes from the brain parenchyma to cervical lymph nodes is along basement membranes in the walls of cerebral capillaries and tunica media of arteries. Perivascular pathways are also involved in the entry of CSF into the brain by the convective influx/glymphatic system. The objective of this study is to differentiate the cerebral vascular basement membrane pathways by which fluid passes out of the brain from the pathway by which CSF enters the brain. Experiment 1: 0.5 µl of soluble biotinylated or fluorescent Aβ, or 1 µl 15 nm gold nanoparticles was injected into the mouse hippocampus and their distributions determined at 5 min by transmission electron microscopy. Aβ was distributed within the extracellular spaces of the hippocampus and within basement membranes of capillaries and tunica media of arteries. Nanoparticles did not enter capillary basement membranes from the extracellular spaces. Experiment 2: 2 µl of 15 nm nanoparticles were injected into mouse CSF. Within 5min, groups of nanoparticles were present in the pial-glial basement membrane on the outer aspect of cortical arteries between the investing layer of pia mater and the glia limitans. The results of this study and previous research suggest that cerebral vascular basement membranes form the pathways by which fluid passes into and out of the brain but that different basement membrane layers are involved. The significance of these findings for neuroimmunology, Alzheimer’s disease, drug delivery to the brain and the concept of the Virchow–Robin space are discussed.</description><identifier>ISSN: 0001-6322</identifier><identifier>EISSN: 1432-0533</identifier><identifier>DOI: 10.1007/s00401-016-1555-z</identifier><identifier>PMID: 26975356</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Actins - metabolism ; Alzheimer's disease ; Amyloid beta-Peptides - metabolism ; Amyloid beta-Peptides - pharmacokinetics ; Animals ; Antigens ; Basement Membrane - drug effects ; Basement Membrane - metabolism ; Basement Membrane - ultrastructure ; Biotinylation ; Blood vessels ; Blood Vessels - cytology ; Brain ; Cerebrospinal Fluid - drug effects ; Cerebrospinal Fluid - metabolism ; Cisterna Magna - drug effects ; Cisterna Magna - metabolism ; Endothelium ; Extracellular Space - drug effects ; Extracellular Space - metabolism ; Fluorescent Dyes - pharmacokinetics ; Hippocampus - drug effects ; Hippocampus - metabolism ; Hippocampus - ultrastructure ; Laminin - metabolism ; Lymphatic system ; Male ; Medicine ; Medicine & Public Health ; Membranes ; Metal Nanoparticles - administration & dosage ; Metal Nanoparticles - ultrastructure ; Mice ; Mice, Inbred C57BL ; Microscopy, Electron, Transmission ; Nanoparticles ; Neurosciences ; Original Paper ; Pathology ; Peptide Fragments - metabolism ; Peptide Fragments - pharmacokinetics ; Veins & arteries</subject><ispartof>Acta neuropathologica, 2016-05, Vol.131 (5), p.725-736</ispartof><rights>The Author(s) 2016</rights><rights>COPYRIGHT 2016 Springer</rights><rights>Springer-Verlag Berlin Heidelberg 2016</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c570t-f0f75440c0cea402f70cdf570558936d5e436c79da65a6d5d08c9f19b0abdc5f3</citedby><cites>FETCH-LOGICAL-c570t-f0f75440c0cea402f70cdf570558936d5e436c79da65a6d5d08c9f19b0abdc5f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00401-016-1555-z$$EPDF$$P50$$Gspringer$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00401-016-1555-z$$EHTML$$P50$$Gspringer$$Hfree_for_read</linktohtml><link.rule.ids>230,314,780,784,885,27924,27925,41488,42557,51319</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26975356$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Morris, Alan W. J.</creatorcontrib><creatorcontrib>Sharp, Matthew MacGregor</creatorcontrib><creatorcontrib>Albargothy, Nazira J.</creatorcontrib><creatorcontrib>Fernandes, Rute</creatorcontrib><creatorcontrib>Hawkes, Cheryl A.</creatorcontrib><creatorcontrib>Verma, Ajay</creatorcontrib><creatorcontrib>Weller, Roy O.</creatorcontrib><creatorcontrib>Carare, Roxana O.</creatorcontrib><title>Vascular basement membranes as pathways for the passage of fluid into and out of the brain</title><title>Acta neuropathologica</title><addtitle>Acta Neuropathol</addtitle><addtitle>Acta Neuropathol</addtitle><description>In the absence of conventional lymphatics, drainage of interstitial fluid and solutes from the brain parenchyma to cervical lymph nodes is along basement membranes in the walls of cerebral capillaries and tunica media of arteries. Perivascular pathways are also involved in the entry of CSF into the brain by the convective influx/glymphatic system. The objective of this study is to differentiate the cerebral vascular basement membrane pathways by which fluid passes out of the brain from the pathway by which CSF enters the brain. Experiment 1: 0.5 µl of soluble biotinylated or fluorescent Aβ, or 1 µl 15 nm gold nanoparticles was injected into the mouse hippocampus and their distributions determined at 5 min by transmission electron microscopy. Aβ was distributed within the extracellular spaces of the hippocampus and within basement membranes of capillaries and tunica media of arteries. Nanoparticles did not enter capillary basement membranes from the extracellular spaces. Experiment 2: 2 µl of 15 nm nanoparticles were injected into mouse CSF. Within 5min, groups of nanoparticles were present in the pial-glial basement membrane on the outer aspect of cortical arteries between the investing layer of pia mater and the glia limitans. The results of this study and previous research suggest that cerebral vascular basement membranes form the pathways by which fluid passes into and out of the brain but that different basement membrane layers are involved. The significance of these findings for neuroimmunology, Alzheimer’s disease, drug delivery to the brain and the concept of the Virchow–Robin space are discussed.</description><subject>Actins - metabolism</subject><subject>Alzheimer's disease</subject><subject>Amyloid beta-Peptides - metabolism</subject><subject>Amyloid beta-Peptides - pharmacokinetics</subject><subject>Animals</subject><subject>Antigens</subject><subject>Basement Membrane - drug effects</subject><subject>Basement Membrane - metabolism</subject><subject>Basement Membrane - ultrastructure</subject><subject>Biotinylation</subject><subject>Blood vessels</subject><subject>Blood Vessels - cytology</subject><subject>Brain</subject><subject>Cerebrospinal Fluid - drug effects</subject><subject>Cerebrospinal Fluid - metabolism</subject><subject>Cisterna Magna - drug effects</subject><subject>Cisterna Magna - metabolism</subject><subject>Endothelium</subject><subject>Extracellular Space - drug effects</subject><subject>Extracellular Space - metabolism</subject><subject>Fluorescent Dyes - pharmacokinetics</subject><subject>Hippocampus - drug effects</subject><subject>Hippocampus - metabolism</subject><subject>Hippocampus - ultrastructure</subject><subject>Laminin - metabolism</subject><subject>Lymphatic system</subject><subject>Male</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Membranes</subject><subject>Metal Nanoparticles - administration & dosage</subject><subject>Metal Nanoparticles - ultrastructure</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Microscopy, Electron, Transmission</subject><subject>Nanoparticles</subject><subject>Neurosciences</subject><subject>Original Paper</subject><subject>Pathology</subject><subject>Peptide Fragments - metabolism</subject><subject>Peptide Fragments - pharmacokinetics</subject><subject>Veins & arteries</subject><issn>0001-6322</issn><issn>1432-0533</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNqNkk1rFTEUhoMo9lr9AW4k4MbN1JOvyWQjlOIXFNyoCzchk0nuTZlJrslMpf31Zri1tqIgWRxyzvO-JIcXoecETgiAfF0AOJAGSNsQIURz_QBtCGe0AcHYQ7QBqNOWUXqEnpRyUW9UcvEYHdFWScFEu0Hfvppil9Fk3JviJhdnPLmpzya6gk3BezPvfpirgn3KeN652ijFbB1OHvtxCQMOcU7YxAGnZV67K1T1IT5Fj7wZi3t2U4_Rl3dvP599aM4_vf94dnreWCFhbjx4KTgHC9YZDtRLsIOvIyE6xdpBOM5aK9VgWmHqdYDOKk9UD6YfrPDsGL05-O6XfnKDrX_IZtT7HCaTr3QyQd-fxLDT23SpeceEAFUNXt0Y5PR9cWXWUyjWjWNdQlqKJrKTSipF_gulHeO1VPTlH-hFWnKsm1gpImknuPxNbc3odIg-1Sfa1VSfcq6UUJK2lTr5C1XP4KZgU3Q-1P49ATkIbE6lZOdv10FAr9nRh-zomh29ZkdfV82Lu3u8VfwKSwXoASh1FLcu3_nRP11_AgL4zmc</recordid><startdate>20160501</startdate><enddate>20160501</enddate><creator>Morris, Alan W. 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J.</creatorcontrib><creatorcontrib>Sharp, Matthew MacGregor</creatorcontrib><creatorcontrib>Albargothy, Nazira J.</creatorcontrib><creatorcontrib>Fernandes, Rute</creatorcontrib><creatorcontrib>Hawkes, Cheryl A.</creatorcontrib><creatorcontrib>Verma, Ajay</creatorcontrib><creatorcontrib>Weller, Roy O.</creatorcontrib><creatorcontrib>Carare, Roxana O.</creatorcontrib><collection>Springer Nature OA Free Journals</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Neurosciences Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Psychology Database (Alumni)</collection><collection>ProQuest Pharma Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Psychology Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest One Psychology</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Acta neuropathologica</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Morris, Alan W. J.</au><au>Sharp, Matthew MacGregor</au><au>Albargothy, Nazira J.</au><au>Fernandes, Rute</au><au>Hawkes, Cheryl A.</au><au>Verma, Ajay</au><au>Weller, Roy O.</au><au>Carare, Roxana O.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Vascular basement membranes as pathways for the passage of fluid into and out of the brain</atitle><jtitle>Acta neuropathologica</jtitle><stitle>Acta Neuropathol</stitle><addtitle>Acta Neuropathol</addtitle><date>2016-05-01</date><risdate>2016</risdate><volume>131</volume><issue>5</issue><spage>725</spage><epage>736</epage><pages>725-736</pages><issn>0001-6322</issn><eissn>1432-0533</eissn><abstract>In the absence of conventional lymphatics, drainage of interstitial fluid and solutes from the brain parenchyma to cervical lymph nodes is along basement membranes in the walls of cerebral capillaries and tunica media of arteries. Perivascular pathways are also involved in the entry of CSF into the brain by the convective influx/glymphatic system. The objective of this study is to differentiate the cerebral vascular basement membrane pathways by which fluid passes out of the brain from the pathway by which CSF enters the brain. Experiment 1: 0.5 µl of soluble biotinylated or fluorescent Aβ, or 1 µl 15 nm gold nanoparticles was injected into the mouse hippocampus and their distributions determined at 5 min by transmission electron microscopy. Aβ was distributed within the extracellular spaces of the hippocampus and within basement membranes of capillaries and tunica media of arteries. Nanoparticles did not enter capillary basement membranes from the extracellular spaces. Experiment 2: 2 µl of 15 nm nanoparticles were injected into mouse CSF. Within 5min, groups of nanoparticles were present in the pial-glial basement membrane on the outer aspect of cortical arteries between the investing layer of pia mater and the glia limitans. The results of this study and previous research suggest that cerebral vascular basement membranes form the pathways by which fluid passes into and out of the brain but that different basement membrane layers are involved. The significance of these findings for neuroimmunology, Alzheimer’s disease, drug delivery to the brain and the concept of the Virchow–Robin space are discussed.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>26975356</pmid><doi>10.1007/s00401-016-1555-z</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Actins - metabolism Alzheimer's disease Amyloid beta-Peptides - metabolism Amyloid beta-Peptides - pharmacokinetics Animals Antigens Basement Membrane - drug effects Basement Membrane - metabolism Basement Membrane - ultrastructure Biotinylation Blood vessels Blood Vessels - cytology Brain Cerebrospinal Fluid - drug effects Cerebrospinal Fluid - metabolism Cisterna Magna - drug effects Cisterna Magna - metabolism Endothelium Extracellular Space - drug effects Extracellular Space - metabolism Fluorescent Dyes - pharmacokinetics Hippocampus - drug effects Hippocampus - metabolism Hippocampus - ultrastructure Laminin - metabolism Lymphatic system Male Medicine Medicine & Public Health Membranes Metal Nanoparticles - administration & dosage Metal Nanoparticles - ultrastructure Mice Mice, Inbred C57BL Microscopy, Electron, Transmission Nanoparticles Neurosciences Original Paper Pathology Peptide Fragments - metabolism Peptide Fragments - pharmacokinetics Veins & arteries |
title | Vascular basement membranes as pathways for the passage of fluid into and out of the brain |
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