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Small noncoding RNA profiling across cellular and biofluid compartments and their implications for multiple sclerosis immunopathology

Zheleznyakova, Galina Yurevna (author)
Piket, Eliane (author)
Karolinska Institutet
Needhamsen, Maria (author)
Karolinska Institutet
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Hagemann-Jensen, Michael (author)
Karolinska Institutet
Ekman, Diana (author)
Stockholms universitet,Institutionen för biokemi och biofysik,Science for Life Laboratory (SciLifeLab)
Han, Yanan (author)
Karolinska Institutet
James, Tojo (author)
Karolinska Institutet
Khademi, Mohsen (author)
Karolinska Institutet
Al Nimer, Faiez (author)
Karolinska Institutet
Scicluna, Patrick (author)
Huang, Jesse (author)
Kockum, Ingrid (author)
Karolinska Institutet
Faridani, Omid R. (author)
Karolinska Institutet
Olsson, Tomas (author)
Karolinska Institutet
Piehl, Fredrik (author)
Karolinska Institutet
Jagodic, Maja (author)
Karolinska Institutet
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 (creator_code:org_t)
2021-04-20
2021
English.
In: Proceedings of the National Academy of Sciences of the United States of America. - : Proceedings of the National Academy of Sciences. - 0027-8424 .- 1091-6490. ; 118:17
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Multiple sclerosis (MS) is a chronic inflammatory demyelinating disease affecting the central nervous system (CNS). Small non-coding RNAs (sncRNAs) and, in particular, microRNAs (miRNAs) have frequently been associated with MS. Here, we performed a comprehensive analysis of all classes of sncRNAs in matching samples of peripheral blood mononuclear cells (PBMCs), plasma, cerebrospinal fluid (CSF) cells, and cell-free CSF from relapsing-remitting (RRMS, n = 12 in relapse and n = 11 in remission) patients, secondary progressive (SPMS, n = 6) MS patients, and noninflammatory and inflammatory neurological disease controls (NINDC, n = 11; INDC, n = 5). We show widespread changes in miRNAs and sncRNA-derived fragments of small nuclear, nucleolar, and transfer RNAs. In CSF cells, 133 out of 133 and 115 out of 117 differentially expressed sncRNAs were increased in RRMS relapse compared to remission and RRMS compared to NINDC, respectively. In contrast, 65 out of 67 differentially expressed PBMC sncRNAs were decreased in RRMS compared to NINDC. The striking contrast between the periphery and CNS suggests that sncRNA-mediated mechanisms, including alternative splicing, RNA degradation, and mRNA translation, regulate the transcriptome of pathogenic cells primarily in the CNS target organ.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Cell- och molekylärbiologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Cell and Molecular Biology (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Immunologi inom det medicinska området (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Immunology in the medical area (hsv//eng)

Keyword

multiple sclerosis
microRNAs
small noncoding RNAs

Publication and Content Type

ref (subject category)
art (subject category)

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