Näytä suppeat kuvailutiedot

dc.contributor.authorHuuska, Nora
dc.contributor.authorNetti, Eliisa
dc.contributor.authorLehti, Satu
dc.contributor.authorKovanen, Petri T.
dc.contributor.authorNiemelä, Mika
dc.contributor.authorTulamo, Riikka
dc.date.accessioned2022-09-14T05:18:39Z
dc.date.available2022-09-14T05:18:39Z
dc.date.issued2022
dc.identifier.citationHuuska, N., Netti, E., Lehti, S., Kovanen, P. T., Niemelä, M., & Tulamo, R. (2022). Lymphatic vessels are present in human saccular intracranial aneurysms. <i>Acta Neuropathologica Communications</i>, <i>10</i>, Article 130. <a href="https://doi.org/10.1186/s40478-022-01430-8" target="_blank">https://doi.org/10.1186/s40478-022-01430-8</a>
dc.identifier.otherCONVID_155950461
dc.identifier.urihttps://jyx.jyu.fi/handle/123456789/83232
dc.description.abstractSaccular intracranial aneurysm (sIA) rupture leads to subarachnoid haemorrhage and is preceded by chronic inflammation and atherosclerotic changes of the sIA wall. Increased lymphangiogenesis has been detected in atherosclerotic extracranial arteries and in abdominal aortic aneurysms, but the presence of lymphatic vessels in sIAs has remained unexplored. Here we studied the presence of lymphatic vessels in 36 intraoperatively resected sIAs (16 unruptured and 20 ruptured), using immunohistochemical and immunofluorescence stainings for lymphatic endothelial cell (LEC) markers. Of these LEC-markers, both extracellular and intracellular LYVE-1-, podoplanin-, VEGFR-3-, and Prox1-positive stainings were detected in 83%, 94%, 100%, and 72% of the 36 sIA walls, respectively. Lymphatic vessels were identified as ring-shaped structures positive for one or more of the LEC markers. Of the sIAs, 78% contained lymphatic vessels positive for at least one LEC marker. The presence of LECs and lymphatic vessels were associated with the number of CD68+ and CD163+  cells in the sIA walls, and with the expression of inflammation indicators such as serum amyloid A, myeloperoxidase, and cyclo-oxygenase 2, with the presence of a thrombus, and with the sIA wall rupture. Large areas of VEGFR-3 and α-smooth muscle actin (αSMA) double-positive cells were detected in medial parts of the sIA walls. Also, a few podoplanin and αSMA double-positive cells were discovered. In addition, LYVE-1 and CD68 double-positive cells were detected in the sIA walls and in the thrombus revealing that certain CD68+ macrophages are capable of expressing LEC markers. This study demonstrates for the first time the presence of lymphatic vessels in human sIA walls. Further studies are needed to understand the role of lymphatic vessels in the pathogenesis of sIA.en
dc.format.mimetypeapplication/pdf
dc.language.isoeng
dc.publisherBiomed Central
dc.relation.ispartofseriesActa Neuropathologica Communications
dc.rightsCC BY 4.0
dc.subject.otherlymphangiogenesis
dc.subject.otherlymphatic vessels
dc.subject.othersaccular intracranial aneurysm
dc.subject.otherinflammation
dc.subject.othercerebral aneurysm
dc.titleLymphatic vessels are present in human saccular intracranial aneurysms
dc.typearticle
dc.identifier.urnURN:NBN:fi:jyu-202209144578
dc.contributor.laitosLiikuntatieteellinen tiedekuntafi
dc.contributor.laitosFaculty of Sport and Health Sciencesen
dc.contributor.oppiaineGerontologian tutkimuskeskusfi
dc.contributor.oppiaineHyvinvoinnin tutkimuksen yhteisöfi
dc.contributor.oppiaineGerontology Research Centeren
dc.contributor.oppiaineSchool of Wellbeingen
dc.type.urihttp://purl.org/eprint/type/JournalArticle
dc.type.coarhttp://purl.org/coar/resource_type/c_2df8fbb1
dc.description.reviewstatuspeerReviewed
dc.relation.issn2051-5960
dc.relation.volume10
dc.type.versionpublishedVersion
dc.rights.copyright© The Author(s) 2022
dc.rights.accesslevelopenAccessfi
dc.subject.ysobiomarkkerit
dc.subject.ysotulehdus
dc.subject.ysoaneurysma
dc.subject.ysoimusuonisto
dc.subject.ysoaivoverenvuoto
dc.subject.ysokallonsisäinen aneurysma
dc.format.contentfulltext
jyx.subject.urihttp://www.yso.fi/onto/yso/p12288
jyx.subject.urihttp://www.yso.fi/onto/yso/p1049
jyx.subject.urihttp://www.yso.fi/onto/yso/p23458
jyx.subject.urihttp://www.yso.fi/onto/yso/p9231
jyx.subject.urihttp://www.yso.fi/onto/yso/p1712
jyx.subject.urihttp://www.yso.fi/onto/yso/p27425
dc.rights.urlhttps://creativecommons.org/licenses/by/4.0/
dc.relation.doi10.1186/s40478-022-01430-8
jyx.fundinginformationThis work was supported by the Helsinki University Hospital EVO Grant No. TYH2021323, Maire Taponen Foundation, the Finnish Medical Foundation, and Petri Honkanen Foundation. Wihuri Research Institute is maintained by the Jenny and Antti Wihuri Foundation.
dc.type.okmA1


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