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Altered IL-32 Signaling in Abdominal Aortic Aneurysm.
Bengts, Sophy; Shamoun, Levar; Kunath, Anne; Appelgren, Daniel; Welander, Martin; Björck, Martin; Wanhainen, Anders; Wågsäter, Dick.
Afiliação
  • Bengts S; Division of Drug Research, Department of Medical and Health Sciences, Linköping University, Linköping, Sweden.
  • Shamoun L; Division of Medical Diagnostics, Department of Laboratory Medicine, Jönköping County, Jönköping, Sweden.
  • Kunath A; Department of Medical Cell Biology, Uppsala University, Uppsala, Sweden.
  • Appelgren D; Department of Medical Cell Biology, Uppsala University, Uppsala, Sweden.
  • Welander M; Division of Drug Research, Department of Medical and Health Sciences, Linköping University, Linköping, Sweden.
  • Björck M; Division of Cardiovascular Medicine, Department of Medical and Health Sciences, Linköping University, Linköping, Sweden.
  • Wanhainen A; Department of Surgical Sciences, Section of Vascular Surgery, Uppsala University, Uppsala, Sweden.
  • Wågsäter D; Department of Surgical Sciences, Section of Vascular Surgery, Uppsala University, Uppsala, Sweden.
J Vasc Res ; 57(4): 236-244, 2020.
Article em En | MEDLINE | ID: mdl-32434199
INTRODUCTION AND OBJECTIVE: Interleukin (IL)-32 is a pro-inflammatory cytokine not previously studied in relation to abdominal aortic aneurysm (AAA). The aim of this study was to elucidate the expression and localization of IL-32 in AAA. METHODS: Expression and localization of IL-32 in human aortic tissue was studied with immunohistochemical analysis and Western blot (AAA: n = 5; controls: n = 4). ELISA was used to measure IL-32 in human plasma samples (AAA: n = 140; controls: n = 37) and in media from cultured peripheral blood mononuclear cells (PBMCs) from 3 healthy donors. IL-32 mRNA in PBMCs, endothelial cells, aortic smooth muscle cells (SMCs), and aortic tissue samples of AAA (n = 16) and control aortas (n = 9) was measured with qPCR. RESULTS: IL-32 was predominantly expressed in SMCs and T-cell-rich areas. Highest mRNA expression was observed in the intima/media layer of the AAA. A weaker protein expression was detected in non-aneurysmal aortas. Expression of IL-32 was confirmed in isolated T cells, macrophages, endothelial cells, and SMCs, where expression was also inducible by cytokines such as interferon-γ. There was no difference in IL-32 expression in plasma between patients and controls. CONCLUSION: IL-32 signaling is altered locally in AAA and could potentially play an important role in aneurysm development. Further studies using animal models would be helpful to study its potential role in AAA disease.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Aorta Abdominal / Interleucinas / Aneurisma da Aorta Abdominal Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: J Vasc Res Assunto da revista: ANGIOLOGIA Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Suécia

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Aorta Abdominal / Interleucinas / Aneurisma da Aorta Abdominal Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: J Vasc Res Assunto da revista: ANGIOLOGIA Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Suécia