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Sökning: onr:"swepub:oai:DiVA.org:uu-442178" > COX-1 dependent bio...

COX-1 dependent biosynthesis of 15-hydroxyeicosatetraenoic acid in human mast cells

Johnsson, Anna-Karin (författare)
Karolinska Institutet
Rönnberg, Elin (författare)
Karolinska Institutet
Fuchs, David (författare)
Karolinska Inst, Dept Med Biochem & Biophys, Div Physiol Chem 2, Stockholm, Sweden.
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Kolmert, Johan (författare)
Karolinska Institutet
Säfholm, Jesper (författare)
Karolinska Institutet
Claesson, Hans-Erik (författare)
Karolinska Institutet
Hamberg, Mats (författare)
Karolinska Institutet
Wheelock, Craig E. (författare)
Karolinska Institutet
Nilsson, Gunnar (författare)
Karolinska Institutet,Uppsala universitet,Hematologi,Karolinska Inst, Immunol & Allergy Div, Dept Med, Stockholm, Sweden.;Karolinska Univ Hosp Solna, Stockholm, Sweden.;Karolinska Inst, Ctr Allergy Res, Stockholm, Sweden.
Dahlén, Sven-Erik (författare)
Karolinska Institutet
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Karolinska Institutet Karolinska Inst, Dept Med Biochem & Biophys, Div Physiol Chem 2, Stockholm, Sweden (creator_code:org_t)
Elsevier, 2021
2021
Engelska.
Ingår i: Biochimica et Biophysica Acta - Molecular and Cell Biology of Lipids. - : Elsevier. - 1388-1981 .- 1879-2618. ; 1866:5
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • 15-hydroxyeicosatetraenoic acid (15-HETE) is an arachidonic acid derived lipid mediator which can originate both from 15-lipoxygenase (15-LOX) activity and cyclooxygenase (COX) activity. The enzymatic source determines the enantiomeric profile of the 15-HETE formed. 15-HETE is the most abundant arachidonic acid metabolite in the human lung and has been suggested to influence the pathophysiology of asthma. Mast cells are central effectors in asthma, but there are contradictory reports on whether 15-HETE originates from 15-LOX or COX in human mast cells. This prompted the current study where the pathway of 15-HETE biosynthesis was examined in three human mast cell models; the cell line LAD2, cord blood derived mast cells (CBMC) and tissue isolated human lung mast cells (HLMC). Levels and enantiomeric profiles of 15-HETE and levels of the downstream metabolite 15-KETE, were analyzed by UPLC-MS/MS after stimulation with anti-IgE or calcium ionophore A23187 in the presence and absence of inhibitors of COX isoenzymes. We found that 15-HETE was produced by COX-1 in human mast cells under these experimental conditions. Unexpectedly, chiral analysis showed that the 15(R) isomer was predominant and gradually accumulated, whereas the 15(S) isomer was metabolized by the 15hydroxyprostaglandin dehydrogenase. We conclude that during physiological conditions, i.e., without addition of exogenous arachidonic acid, both enantiomers of 15-HETE are produced by COX-1 in human mast cells but that the 15(S) isomer is selectively depleted by undergoing further metabolism. The study highlights that 15-HETE cannot be used as an indicator of 15-LOX activity for cellular studies, unless chirality and sensitivity to pharmacologic inhibition is determined.

Ämnesord

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

Nyckelord

Prostanoids
Eicosanoids
15-KETE
Mass spectrometry
Mediators of allergy

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