Abstract | INTRODUCTION: MATERIALS AND METHODS: Human atherosclerotic plaques from carotid endarterectomies were used for mRNA and immunohistochemistry analyses. hPBMCs isolated from buffy coats and THP-1 cells were differentiated and polarized into M1 or M2 macrophages, and subsequently cultured with or without cholesterol crystals (CC). mRNA and protein expression were measured with qRT-PCR and ELISA, respectively, and procoagulant activity was assessed using a two-stage chromogenic assay. RESULTS: TFPIα and TFPIβ mRNA levels were significantly increased in carotid plaques, whereas TF levels were unchanged as compared to healthy arteries. Antibodies against total TFPI showed elevated levels compared to antibodies against free TFPIα, both by immunohistochemical and ELISA detection in plaques. The antibody against total TFPI also co-localized with CD68 and the M1 and M2 markers CD80 and CD163, respectively. The TFPI mRNA expression was elevated and the procoagulant activity was decreased in M2 compared to M1 polarized human macrophages. TFPI was present in early foam cell formation and CC treatment increased the TFPI mRNA expression even further in M2 macrophages. CONCLUSIONS: Our data indicate that both isoforms of TFPI are present in advanced plaques and that anti-inflammatory M2 macrophages may be a potential source of TFPI.
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Authors | Benedicte Stavik, Sverre Holm, Sandra Espada, Nina Iversen, Bjørnar Sporsheim, Vigdis Bjerkeli, Tuva Børresdatter Dahl, Per Morten Sandset, Mona Skjelland, Terje Espevik, Grethe Skretting, Bente Halvorsen |
Journal | Thrombosis research
(Thromb Res)
Vol. 155
Pg. 31-37
(Jul 2017)
ISSN: 1879-2472 [Electronic] United States |
PMID | 28482260
(Publication Type: Journal Article)
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Copyright | Copyright © 2017 Elsevier Ltd. All rights reserved. |
Chemical References |
- Lipoproteins
- Protein Isoforms
- RNA, Messenger
- lipoprotein-associated coagulation inhibitor
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Topics |
- Carotid Arteries
(metabolism, pathology)
- Carotid Stenosis
(genetics, pathology)
- Cell Line
- Cells, Cultured
- Humans
- Lipoproteins
(genetics)
- Macrophages
(metabolism, pathology)
- Plaque, Atherosclerotic
(genetics, pathology)
- Protein Isoforms
(genetics)
- RNA, Messenger
(genetics)
- Up-Regulation
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