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Sökning: WFRF:(Kramann Rafael) > (2019) > Heterogeneity and p...

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FältnamnIndikatorerMetadata
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001oai:DiVA.org:uu-396467
003SwePub
008191114s2019 | |||||||||||000 ||eng|
009oai:prod.swepub.kib.ki.se:142108486
024a https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-3964672 URI
024a https://doi.org/10.1093/cvr/cvz1852 DOI
024a http://kipublications.ki.se/Default.aspx?queryparsed=id:1421084862 URI
040 a (SwePub)uud (SwePub)ki
041 a engb eng
042 9 SwePub
072 7a ref2 swepub-contenttype
072 7a for2 swepub-publicationtype
100a van Kuijk, Kimu MUMC Maastricht, CARIM Sch Cardiovasc Dis, Pathol Dept, P Debyelaan 25, NL-6229HX Maastricht, Netherlands4 aut
2451 0a Heterogeneity and plasticity in healthy and atherosclerotic vasculature explored by single-cell sequencing
264 c 2019-07-27
264 1b Oxford University Press,c 2019
338 a print2 rdacarrier
520 a Cellular characteristics and their adjustment to a state of disease have become more evident due to recent advances in imaging, fluorescent reporter mice, and whole genome RNA sequencing. The uncovered cellular heterogeneity and/or plasticity potentially complicates experimental studies and clinical applications, as markers derived from whole tissue 'bulk' sequencing is unable to yield a subtype transcriptome and specific markers. Here, we propose definitions on heterogeneity and plasticity, discuss current knowledge thereof in the vasculature and how this may be improved by single-cell sequencing (SCS). SCS is emerging as an emerging technique, enabling researchers to investigate different cell populations in more depth than ever before. Cell selection methods, e.g. flow assisted cell sorting, and the quantity of cells can influence the choice of SCS method. Smart-Seq2 offers sequencing of the complete mRNA molecule on a low quantity of cells, while Drop-seq is possible on large numbers of cells on a more superficial level. SCS has given more insight in heterogeneity in healthy vasculature, where it revealed that zonation is crucial in gene expression profiles among the anatomical axis. In diseased vasculature, this heterogeneity seems even more prominent with discovery of new immune subsets in atherosclerosis as proof. Vascular smooth muscle cells and mesenchymal cells also share these plastic characteristics with the ability to up-regulate markers linked to stem cells, such as Sca-1 or CD34. Current SCS studies show some limitations to the number of replicates, quantity of cells used, or the loss of spatial information. Bioinformatical tools could give some more insight in current datasets, making use of pseudo-time analysis or RNA velocity to investigate cell differentiation or polarization. In this review, we discuss the use of SCS in unravelling heterogeneity in the vasculature, its current limitations and promising future applications.
650 7a MEDICIN OCH HÄLSOVETENSKAPx Medicinska och farmaceutiska grundvetenskaperx Cell- och molekylärbiologi0 (SwePub)301082 hsv//swe
650 7a MEDICAL AND HEALTH SCIENCESx Basic Medicinex Cell and Molecular Biology0 (SwePub)301082 hsv//eng
653 a Heterogeneity
653 a Single-cell sequencing
653 a Vasculature
653 a Atherosclerosis
700a Kuppe, Christophu Rhein Westfal TH Aachen, Biochem Dept, Aachen, Germany4 aut
700a Betsholtz, Christeru Uppsala universitet,Vaskulärbiologi,Karolinska Inst Stockholm, Integrated Cardio Metab Ctr, Stockholm, Sweden4 aut0 (Swepub:uu)chbet517
700a Vanlandewijck, Michael,d 1982-u Uppsala universitet,Vaskulärbiologi,Karolinska Inst Stockholm, Integrated Cardio Metab Ctr, Stockholm, Sweden4 aut0 (Swepub:uu)micva660
700a Kramann, Rafaelu Rhein Westfal TH Aachen, Biochem Dept, Aachen, Germany4 aut
700a Sluimer, Judith C.u MUMC Maastricht, CARIM Sch Cardiovasc Dis, Pathol Dept, P Debyelaan 25, NL-6229HX Maastricht, Netherlands;Univ Edinburgh, British Heart Fdn, Ctr Cardiovasc Sci CVS, Edinburgh, Midlothian, Scotland4 aut
710a MUMC Maastricht, CARIM Sch Cardiovasc Dis, Pathol Dept, P Debyelaan 25, NL-6229HX Maastricht, Netherlandsb Rhein Westfal TH Aachen, Biochem Dept, Aachen, Germany4 org
773t Cardiovascular Researchd : Oxford University Pressg 115:12, s. 1705-1715q 115:12<1705-1715x 0008-6363x 1755-3245
856u https://academic.oup.com/cardiovascres/article-pdf/115/12/1705/31082806/cvz185.pdf
8564 8u https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-396467
8564 8u https://doi.org/10.1093/cvr/cvz185
8564 8u http://kipublications.ki.se/Default.aspx?queryparsed=id:142108486

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