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Inhibition of 12-lipoxygenase reduces platelet activation and prevents their mitogenic function

Svensson Holm, Ann-Charlotte (author)
Linköpings universitet,Avdelningen för cellbiologi,Avdelningen för läkemedelsforskning,Hälsouniversitetet
Grenegård, Magnus, 1963- (author)
Linköpings universitet,Örebro universitet,Institutionen för läkarutbildning,Department of Medical and Health Sciences, Faculty of Health Sciences, Linköping University, Linköping, Sweden; Department of Clinical Pathology and Clinical Genetics, County Council of Östergötland, Linköping, Sweden,Avdelningen för läkemedelsforskning,Hälsouniversitetet,Örebro University, Sweden
Ollinger, Karin (author)
Östergötlands Läns Landsting,Linköpings universitet,Avdelningen för cellbiologi,Hälsouniversitetet,Klinisk patologi och klinisk genetik
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Lindström, Eva (author)
Linköpings universitet,Avdelningen för läkemedelsforskning,Hälsouniversitetet
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 (creator_code:org_t)
2013-03-27
2014
English.
In: Platelets. - London, United Kingdom : Informa Healthcare. - 0953-7104 .- 1369-1635. ; 25:2, s. 111-117
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • The aim of the present study was to investigate the role of 12-lipoxygenase (12-LOX) on platelet-induced airway smooth muscle cell (ASMC) proliferation. Co-incubation of platelets and ASMC caused platelet activation as determined by morphological changes. Simultaneously, reactive oxygen species (ROS)-generation was detected and ASMC proliferation (measured by using the MTS assay) increased significantly. Furthermore, we found that the 12-LOX inhibitors cinnamyl-3,4-dihydroxy-a-cyanocinnamate (CDC) and Baicalein prevented platelet activation in a co-cultures of platelets and ASMC. The inhibitory effect of CDC and Baicalein on platelets was also registered in a pure platelet preparation. Specifically, the 12-LOX inhibitors reduced collagen-induced platelet aggregation both in the presence and absence of external added fibrinogen. Importantly, platelet-induced ASMC proliferation and ROS production generated during the platelet/ASMC interaction was significantly inhibited in the presence of 12-LOX inhibitors. In conclusion, our findings reveal that 12-LOX is crucial for the observed enhancement of ASMC proliferation in co-cultures of platelets and ASMC. The present result suggests that 12-LOX activity is important in the initial step of platelet/ASMC interaction and platelet activation. Such action of 12-LOX represents a potential important mechanism that may contribute to platelet-induced airway remodelling.

Subject headings

NATURVETENSKAP  -- Biologi -- Cellbiologi (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences -- Cell Biology (hsv//eng)

Keyword

12-lipoxygenase
airway remodelling
airway smooth muscle
platelet-induced proliferation
Cellforskning
Cell Research
Medicine
Medicin

Publication and Content Type

ref (subject category)
art (subject category)

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