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Sökning: WFRF:(Harris Robert A) > (2020-2024) > Altered perivascula...

LIBRIS Formathandbok  (Information om MARC21)
FältnamnIndikatorerMetadata
00008248naa a2200817 4500
001oai:DiVA.org:umu-182762
003SwePub
008210511s2021 | |||||||||||000 ||eng|
009oai:DiVA.org:kth-295441
009oai:prod.swepub.kib.ki.se:146460728
024a https://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-1827622 URI
024a https://doi.org/10.1038/s41591-021-01295-92 DOI
024a https://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-2954412 URI
024a http://kipublications.ki.se/Default.aspx?queryparsed=id:1464607282 URI
040 a (SwePub)umud (SwePub)kthd (SwePub)ki
041 a engb eng
042 9 SwePub
072 7a ref2 swepub-contenttype
072 7a art2 swepub-publicationtype
100a Månberg, Anna,d 1985-u KTH,Science for Life Laboratory, SciLifeLab,Affinitets-proteomik4 aut0 (Swepub:kth)u1g5roxd
2451 0a Altered perivascular fibroblast activity precedes ALS disease onset
264 c 2021-04-15
264 1b Nature Publishing Group,c 2021
338 a print2 rdacarrier
500 a Publisher Correction:Månberg, A., Skene, N., Sanders, F. et al. Publisher Correction: Altered perivascular fibroblast activity precedes ALS disease onset. Nat Med 27, 1308 (2021). DOI: 10.1038/s41591-021-01414-6
500 a QC 20210621
520 a Apart from well-defined factors in neuronal cells1, only a few reports consider that the variability of sporadic amyotrophic lateral sclerosis (ALS) progression can depend on less-defined contributions from glia2,3 and blood vessels4. In this study we use an expression-weighted cell-type enrichment method to infer cell activity in spinal cord samples from patients with sporadic ALS and mouse models of this disease. Here we report that patients with sporadic ALS present cell activity patterns consistent with two mouse models in which enrichments of vascular cell genes preceded microglial response. Notably, during the presymptomatic stage, perivascular fibroblast cells showed the strongest gene enrichments, and their marker proteins SPP1 and COL6A1 accumulated in enlarged perivascular spaces in patients with sporadic ALS. Moreover, in plasma of 574 patients with ALS from four independent cohorts, increased levels of SPP1 at disease diagnosis repeatedly predicted shorter survival with stronger effect than the established risk factors of bulbar onset or neurofilament levels in cerebrospinal fluid. We propose that the activity of the recently discovered perivascular fibroblast can predict survival of patients with ALS and provide a new conceptual framework to re-evaluate definitions of ALS etiology.
650 7a MEDICIN OCH HÄLSOVETENSKAPx Medicinska och farmaceutiska grundvetenskaperx Neurovetenskaper0 (SwePub)301052 hsv//swe
650 7a MEDICAL AND HEALTH SCIENCESx Basic Medicinex Neurosciences0 (SwePub)301052 hsv//eng
650 7a MEDICIN OCH HÄLSOVETENSKAPx Klinisk medicinx Neurologi0 (SwePub)302072 hsv//swe
650 7a MEDICAL AND HEALTH SCIENCESx Clinical Medicinex Neurology0 (SwePub)302072 hsv//eng
700a Skene, Nathanu Department of Medical Biochemistry and Biophysics, Karolinska Institute, Stockholm, Sweden; Division of Neuroscience, Department of Brain Sciences, Imperial College London, London, United Kingdom; United Kingdom Dementia Research Institute, London, United Kingdom4 aut
700a Sanders, Folkertu Department of Clinical Neuroscience, Karolinska Institute, Centre for Molecular Medicine, Karolinska Hospital, Stockholm, Sweden4 aut
700a Trusohamn, Martau Department of Medical Biochemistry and Biophysics, Karolinska Institute, Stockholm, Sweden4 aut
700a Remnestål, Juliau KTH,Affinitets-proteomik,Science for Life Laboratory, SciLifeLab4 aut0 (Swepub:kth)u13wztpi
700a Szczepińska, Annau Karolinska Institutet4 aut
700a Aksoylu, Inci Sevvalu Karolinska Institutet4 aut
700a Lönnerberg, Peteru Karolinska Institutet4 aut
700a Ebarasi, Lwakiu Department of Laboratory Medicine, Karolinska Institute, Stockholm, Sweden4 aut
700a Wouters, Stefanu Department of Clinical Neuroscience, Karolinska Institute, Centre for Molecular Medicine, Karolinska Hospital, Stockholm, Sweden4 aut
700a Lehmann, Manuelau Umeå universitet,Institutionen för integrativ medicinsk biologi (IMB)4 aut0 (Swepub:umu)male0080
700a Olofsson, Jennieu KTH,Science for Life Laboratory, SciLifeLab,Affinitets-proteomik4 aut0 (Swepub:kth)u1q8hz5k
700a von Gohren Antequera, Intiu Department of Clinical Neuroscience, Karolinska Institute, Centre for Molecular Medicine, Karolinska Hospital, Stockholm, Sweden4 aut
700a Domaniku, Aylinu Department of Clinical Neuroscience, Karolinska Institute, Centre for Molecular Medicine, Karolinska Hospital, Stockholm, Sweden4 aut
700a De Schaepdryver, Maximu Laboratory for Neurobiomarker Research, Department of Neurology, Leuven Brain Institute, KU Leuven (University of Leuven), Leuven, Belgium4 aut
700a De Vocht, Jokeu Neurology Department and Center for Brain & Disease Research, KU Leuven, VIB, Leuven, Belgium4 aut
700a Poesen, Koenu Laboratory for Neurobiomarker Research, Department of Neurology, Leuven Brain Institute, KU Leuven (University of Leuven), Leuven, Belgium; Laboratory Medicine, UZ Leuven (University Hospital Leuven), Leuven, Belgium4 aut
700a Uhlén, Mathiasu KTH,Science for Life Laboratory, SciLifeLab,Systembiologi,Karolinska Inst, Dept Neurosci, Stockholm, Sweden.4 aut0 (Swepub:kth)u1dulvmw
700a Anink, Jasperu Department of (Neuro)Pathology, Amsterdam UMC, University of Amsterdam, Amsterdam Neuroscience, Amsterdam, Netherlands4 aut
700a Mijnsbergen, Carolineu Department of (Neuro)Pathology, Amsterdam UMC, University of Amsterdam, Amsterdam Neuroscience, Amsterdam, Netherlands4 aut
700a Vergunst-Bosch, Hermienekeu UMC Utrecht Brain Center, University Medical Center Utrecht, Department of Neurology, Utrecht University, Utrecht, Netherlands4 aut
700a Hübers, Annemarieu University of Ulm, Neurology Clinic, Ulm, Germany; Division of Neurology, Geneva University Hospital, Geneva, Switzerland4 aut
700a Kläppe, Ulfu Karolinska Institutet4 aut
700a Rodriguez-Vieitez, Elenau Karolinska Institutet4 aut
700a Gilthorpe, Jonathan D.u Umeå universitet,Institutionen för integrativ medicinsk biologi (IMB)4 aut0 (Swepub:umu)jogi0002
700a Hedlund, Evau Karolinska Institutet4 aut
700a Harris, Robert A.u Karolinska Institutet4 aut
700a Aronica, Eleonorau Department of (Neuro)Pathology, Amsterdam UMC, University of Amsterdam, Amsterdam Neuroscience, Amsterdam, Netherlands4 aut
700a Van Damme, Philipu Neurology Department and Center for Brain & Disease Research, KU Leuven, VIB, Leuven, Belgium4 aut
700a Ludolph, Albertu University of Ulm, Neurology Clinic, Ulm, Germany; Deutsches Zentrum für Neurodegenerative Erkrankungen (DZNE), Ulm, Bonn, Germany4 aut
700a Veldink, Janu UMC Utrecht Brain Center, University Medical Center Utrecht, Department of Neurology, Utrecht University, Utrecht, Netherlands4 aut
700a Ingre, Carolineu Karolinska Institutet4 aut
700a Nilsson, Peteru KTH,Science for Life Laboratory, SciLifeLab,Affinitets-proteomik4 aut0 (Swepub:kth)u1ws88sk
700a Lewandowski, Sebastianu KTH,Affinitets-proteomik,Science for Life Laboratory, SciLifeLab,Department of Clinical Neuroscience, Karolinska Institute, Centre for Molecular Medicine, Karolinska Hospital, Stockholm, Sweden4 aut0 (Swepub:kth)u1d4y8tu
710a KTHb Science for Life Laboratory, SciLifeLab4 org
773t Nature Medicined : Nature Publishing Groupg 27:4, s. 640-646q 27:4<640-646x 1078-8956x 1546-170X
856u http://spiral.imperial.ac.uk/bitstream/10044/1/89868/2/output.pdf
8564 8u https://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-182762
8564 8u https://doi.org/10.1038/s41591-021-01295-9
8564 8u https://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-295441
8564 8u http://kipublications.ki.se/Default.aspx?queryparsed=id:146460728

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