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Complement component C3 and the TLR co-receptor CD14 are not involved in angiotensin II induced cardiac remodelling

Shahini, Negar (author)
Oslo University Hospital, Norway;University of Oslo, Norway
Schjalm, Camilla (author)
Oslo University Hospital, Norway;University of Oslo, Norway
Nilsson, Per H., 1980- (author)
Linnéuniversitetet,Institutionen för kemi och biomedicin (KOB),Avancerade material,Oslo University Hospital, Norway;University of Oslo, Norway,Linnaeus Ctr Biomat Chem, BMC;HoRB
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Holt, Margrethe Flesvig (author)
Oslo University Hospital, Norway;University of Oslo, Norway
Ogaard, Jonas D. S. (author)
Oslo University Hospital, Norway;University of Oslo, Norway
Lien, Egil (author)
UMass Med Sch, USA;Norwegian Univ Sci & Technol, Norway
Ahmed, Muhammad S. (author)
Oslo University Hospital, Norway;University of Oslo, Norway
Attramadal, Havard (author)
Oslo University Hospital, Norway;University of Oslo, Norway
Aukrust, Pal (author)
Oslo University Hospital, Norway;University of Oslo, Norway;Norwegian Univ Sci & Technol, Norway
Yndestad, Arne (author)
Oslo University Hospital, Norway;University of Oslo, Norway
Mollnes, Tom Eirik (author)
Oslo University Hospital, Norway;University of Oslo, Norway;Norwegian Univ Sci & Technol, Norway;Nordland Hosp, Norway;Univ Tromsö, Norway
Louwe, Mieke C. (author)
Oslo University Hospital, Norway;University of Oslo, Norway
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 (creator_code:org_t)
Elsevier, 2020
2020
English.
In: Biochemical and Biophysical Research Communications - BBRC. - : Elsevier. - 0006-291X .- 1090-2104. ; 523:4, s. 867-873
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Inflammation is centrally involved in the development of cardiac hypertrophy and the processes of remodelling. The complement system and Toll-like receptor (TLR) family, two upstream arms of the innate immune system, have previously been reported to be involved in cardiac remodelling. However, the role of complement component 3 (C3), TLR co-receptor CD14 and the synergy between them have not been addressed during pressure overload-induced cardiac remodelling. Here, we examined angiotensin II-induced cardiac hypertrophy and remodelling for 7 days in male C57Bl/6 J mice deficient in C3, CD14, or both (C3CD14), and WT controls. Angiotensin II infusion induced a mild concentric hypertrophic phenotype in WT mice with increased left ventricle weight, wall thicknesses and reduced ventricular internal diameter, associated with increased cardiac fibrosis. However, there were no differences between WT mice and mice deficient for C3, CD14 or C3CD14, as systolic blood pressure, cardiac function and structure and levels of fibrosis were comparable between WT mice and the three other genotypes. C5a did not change in angiotensin II treated mice, whereas Mac2 levels were increased in angiotensin II treated mice, but did not differ between genotypes. The inflammatory IL-6 response was comparable between WT and C3 deficient mice, however, it was decreased in CD14 and C3CD14 deficient mice. We conclude that deficiency in C3, CD14 or C3CD14 had no effect on cardiac remodelling following angiotensin II-induced pressure overload. This suggests that C3 and CD14 are not involved in angiotensin II-induced adverse cardiac remodelling. (C) 2020 Published by Elsevier Inc.

Subject headings

NATURVETENSKAP  -- Biologi -- Biofysik (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences -- Biophysics (hsv//eng)
NATURVETENSKAP  -- Biologi -- Biokemi och molekylärbiologi (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences -- Biochemistry and Molecular Biology (hsv//eng)

Keyword

Complement
Toll-like receptor
C3
CD14
Cardiac remodelling
Angiotensin
Biokemi
Biochemistry

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