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Possible Involvement of Intracellular Calcium-Independent Phospholipase A(2) in the Release of Secretory Phospholipases from Mast Cells—Increased Expression in Ileal Mast Cells of Crohn’s Disease

Increased activity of secretory phospholipases A(2) (sPLA(2)) type-II was previously observed in ileum of Crohn’s disease (CD). Our aims were to explore the involvement of calcium-independent (i)PLA(2)β in the release of sPLA(2)s from the human mast cell (MC) line (HMC-1) and investigate expressions...

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Autores principales: Christerson, Ulrika, Keita, Åsa V., Winberg, Martin E., Söderholm, Johan D., Gustafson-Svärd, Christina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6678282/
https://www.ncbi.nlm.nih.gov/pubmed/31277247
http://dx.doi.org/10.3390/cells8070672
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author Christerson, Ulrika
Keita, Åsa V.
Winberg, Martin E.
Söderholm, Johan D.
Gustafson-Svärd, Christina
author_facet Christerson, Ulrika
Keita, Åsa V.
Winberg, Martin E.
Söderholm, Johan D.
Gustafson-Svärd, Christina
author_sort Christerson, Ulrika
collection PubMed
description Increased activity of secretory phospholipases A(2) (sPLA(2)) type-II was previously observed in ileum of Crohn’s disease (CD). Our aims were to explore the involvement of calcium-independent (i)PLA(2)β in the release of sPLA(2)s from the human mast cell (MC) line (HMC-1) and investigate expressions of cytosolic (c)PLA(2)α, iPLA(2)β, sPLA(2)-IIA and sPLA(2)-V in MCs of CD ileum. The release of sPLA(2) was investigated in HMC-1 by immunocytochemistry and ELISA. The expression intensities of PLA(2)s in mucosal MCs, and the proportion of PLA(2)-positive MCs, were investigated in normal ileum and in ileum from patients with CD by immunohistochemistry. The calcium ionophore-stimulated release of sPLA(2)-IIA and sPLA(2)-V from HMC-1 was reduced by the iPLA(2)-inhibitor bromoenol lactone. All four PLA(2)s were detectable in mucosal MCs, both in normal ileum and in CD, but the proportion of iPLA(2)β-containing mucosal MCs and the expression intensity of sPLA(2)-IIA was increased in CD. Results indicate that iPLA(2)β is involved in the secretion of sPLA(2)s from HMC-1, and suggest that iPLA(2)β-mediated release of sPLA(2) from intestinal MCs may contribute to CD pathophysiology. Ex vivo studies on isolated mucosal mast cells are however needed to clarify the precise role of MC PLA(2)s in the inflammatory processes of CD.
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spelling pubmed-66782822019-08-19 Possible Involvement of Intracellular Calcium-Independent Phospholipase A(2) in the Release of Secretory Phospholipases from Mast Cells—Increased Expression in Ileal Mast Cells of Crohn’s Disease Christerson, Ulrika Keita, Åsa V. Winberg, Martin E. Söderholm, Johan D. Gustafson-Svärd, Christina Cells Article Increased activity of secretory phospholipases A(2) (sPLA(2)) type-II was previously observed in ileum of Crohn’s disease (CD). Our aims were to explore the involvement of calcium-independent (i)PLA(2)β in the release of sPLA(2)s from the human mast cell (MC) line (HMC-1) and investigate expressions of cytosolic (c)PLA(2)α, iPLA(2)β, sPLA(2)-IIA and sPLA(2)-V in MCs of CD ileum. The release of sPLA(2) was investigated in HMC-1 by immunocytochemistry and ELISA. The expression intensities of PLA(2)s in mucosal MCs, and the proportion of PLA(2)-positive MCs, were investigated in normal ileum and in ileum from patients with CD by immunohistochemistry. The calcium ionophore-stimulated release of sPLA(2)-IIA and sPLA(2)-V from HMC-1 was reduced by the iPLA(2)-inhibitor bromoenol lactone. All four PLA(2)s were detectable in mucosal MCs, both in normal ileum and in CD, but the proportion of iPLA(2)β-containing mucosal MCs and the expression intensity of sPLA(2)-IIA was increased in CD. Results indicate that iPLA(2)β is involved in the secretion of sPLA(2)s from HMC-1, and suggest that iPLA(2)β-mediated release of sPLA(2) from intestinal MCs may contribute to CD pathophysiology. Ex vivo studies on isolated mucosal mast cells are however needed to clarify the precise role of MC PLA(2)s in the inflammatory processes of CD. MDPI 2019-07-03 /pmc/articles/PMC6678282/ /pubmed/31277247 http://dx.doi.org/10.3390/cells8070672 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Christerson, Ulrika
Keita, Åsa V.
Winberg, Martin E.
Söderholm, Johan D.
Gustafson-Svärd, Christina
Possible Involvement of Intracellular Calcium-Independent Phospholipase A(2) in the Release of Secretory Phospholipases from Mast Cells—Increased Expression in Ileal Mast Cells of Crohn’s Disease
title Possible Involvement of Intracellular Calcium-Independent Phospholipase A(2) in the Release of Secretory Phospholipases from Mast Cells—Increased Expression in Ileal Mast Cells of Crohn’s Disease
title_full Possible Involvement of Intracellular Calcium-Independent Phospholipase A(2) in the Release of Secretory Phospholipases from Mast Cells—Increased Expression in Ileal Mast Cells of Crohn’s Disease
title_fullStr Possible Involvement of Intracellular Calcium-Independent Phospholipase A(2) in the Release of Secretory Phospholipases from Mast Cells—Increased Expression in Ileal Mast Cells of Crohn’s Disease
title_full_unstemmed Possible Involvement of Intracellular Calcium-Independent Phospholipase A(2) in the Release of Secretory Phospholipases from Mast Cells—Increased Expression in Ileal Mast Cells of Crohn’s Disease
title_short Possible Involvement of Intracellular Calcium-Independent Phospholipase A(2) in the Release of Secretory Phospholipases from Mast Cells—Increased Expression in Ileal Mast Cells of Crohn’s Disease
title_sort possible involvement of intracellular calcium-independent phospholipase a(2) in the release of secretory phospholipases from mast cells—increased expression in ileal mast cells of crohn’s disease
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6678282/
https://www.ncbi.nlm.nih.gov/pubmed/31277247
http://dx.doi.org/10.3390/cells8070672
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