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Vehicle-dependent Effects of Sphingosine 1-phosphate on Plasminogen Activator Inhibitor-1 Expression

Aim: Sphingosine 1-phosphate (S1P) has been suggested to be a positive regulator of plasminogen activator inhibitor 1 (PAI-1) in adipocytes, while some studies are not consistent with this prothrombotic property of S1P. Since S1P is bound to apolipoprotein M (apoM) on HDL or to albumin in plasma, we...

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Autores principales: Takahashi, Chiharu, Kurano, Makoto, Nishikawa, Masako, Kano, Kuniyuki, Dohi, Tomotaka, Miyauchi, Katsumi, Daida, Hiroyuki, Shimizu, Tomo, Aoki, Junken, Yatomi, Yutaka
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Japan Atherosclerosis Society 2017
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5587522/
https://www.ncbi.nlm.nih.gov/pubmed/28321011
http://dx.doi.org/10.5551/jat.37663
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author Takahashi, Chiharu
Kurano, Makoto
Nishikawa, Masako
Kano, Kuniyuki
Dohi, Tomotaka
Miyauchi, Katsumi
Daida, Hiroyuki
Shimizu, Tomo
Aoki, Junken
Yatomi, Yutaka
author_facet Takahashi, Chiharu
Kurano, Makoto
Nishikawa, Masako
Kano, Kuniyuki
Dohi, Tomotaka
Miyauchi, Katsumi
Daida, Hiroyuki
Shimizu, Tomo
Aoki, Junken
Yatomi, Yutaka
author_sort Takahashi, Chiharu
collection PubMed
description Aim: Sphingosine 1-phosphate (S1P) has been suggested to be a positive regulator of plasminogen activator inhibitor 1 (PAI-1) in adipocytes, while some studies are not consistent with this prothrombotic property of S1P. Since S1P is bound to apolipoprotein M (apoM) on HDL or to albumin in plasma, we compared the properties of these two forms on the PAI-1 induction. Methods: We investigated the associations of S1P, apoM, and PAI-1 concentrations in the plasma of normal coronary artery (NCA), stable angina pectoris (SAP), and acute coronary syndrome (ACS) subjects (n = 32, 71, and 38, respectively). Then, we compared the effects of S1P with various vehicles on the PAI-1 expression in 3T3L1 adipocytes. We also investigated the modulation of the PAI-1 levels in mice infected with adenovirus coding apoM. Results: Among ACS subjects, the PAI-1 level was positively correlated with the S1P level, but not the apoM level. In adipocytes, S1P bound to an apoM-rich vehicle induced PAI-1 expression to a lesser extent than the control vehicle, while S1P bound to an apoM-depleted vehicle induced PAI-1 expression to a greater extent than the control vehicle in 3T3L1 adipocytes. Additionally, apoM overexpression in mice failed to modulate the plasma PAI-1 level and the adipose PAI-1 expression level. S1P bound to albumin increased PAI-1 expression through the S1P receptor 2-Rho/ROCK-NFκB pathway. Conclusion: S1P bound to albumin, but not to apoM, induces PAI-1 expression in adipocytes, indicating that S1P can exert different properties on the pathogenesis of vascular diseases, depending on its vehicle.
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spelling pubmed-55875222017-09-11 Vehicle-dependent Effects of Sphingosine 1-phosphate on Plasminogen Activator Inhibitor-1 Expression Takahashi, Chiharu Kurano, Makoto Nishikawa, Masako Kano, Kuniyuki Dohi, Tomotaka Miyauchi, Katsumi Daida, Hiroyuki Shimizu, Tomo Aoki, Junken Yatomi, Yutaka J Atheroscler Thromb Original Article Aim: Sphingosine 1-phosphate (S1P) has been suggested to be a positive regulator of plasminogen activator inhibitor 1 (PAI-1) in adipocytes, while some studies are not consistent with this prothrombotic property of S1P. Since S1P is bound to apolipoprotein M (apoM) on HDL or to albumin in plasma, we compared the properties of these two forms on the PAI-1 induction. Methods: We investigated the associations of S1P, apoM, and PAI-1 concentrations in the plasma of normal coronary artery (NCA), stable angina pectoris (SAP), and acute coronary syndrome (ACS) subjects (n = 32, 71, and 38, respectively). Then, we compared the effects of S1P with various vehicles on the PAI-1 expression in 3T3L1 adipocytes. We also investigated the modulation of the PAI-1 levels in mice infected with adenovirus coding apoM. Results: Among ACS subjects, the PAI-1 level was positively correlated with the S1P level, but not the apoM level. In adipocytes, S1P bound to an apoM-rich vehicle induced PAI-1 expression to a lesser extent than the control vehicle, while S1P bound to an apoM-depleted vehicle induced PAI-1 expression to a greater extent than the control vehicle in 3T3L1 adipocytes. Additionally, apoM overexpression in mice failed to modulate the plasma PAI-1 level and the adipose PAI-1 expression level. S1P bound to albumin increased PAI-1 expression through the S1P receptor 2-Rho/ROCK-NFκB pathway. Conclusion: S1P bound to albumin, but not to apoM, induces PAI-1 expression in adipocytes, indicating that S1P can exert different properties on the pathogenesis of vascular diseases, depending on its vehicle. Japan Atherosclerosis Society 2017-09-01 /pmc/articles/PMC5587522/ /pubmed/28321011 http://dx.doi.org/10.5551/jat.37663 Text en 2017 Japan Atherosclerosis Society This article is distributed under the terms of the latest version of CC BY-NC-SA defined by the Creative Commons Attribution License.http://creativecommons.org/licenses/by-nc-sa/3.0/
spellingShingle Original Article
Takahashi, Chiharu
Kurano, Makoto
Nishikawa, Masako
Kano, Kuniyuki
Dohi, Tomotaka
Miyauchi, Katsumi
Daida, Hiroyuki
Shimizu, Tomo
Aoki, Junken
Yatomi, Yutaka
Vehicle-dependent Effects of Sphingosine 1-phosphate on Plasminogen Activator Inhibitor-1 Expression
title Vehicle-dependent Effects of Sphingosine 1-phosphate on Plasminogen Activator Inhibitor-1 Expression
title_full Vehicle-dependent Effects of Sphingosine 1-phosphate on Plasminogen Activator Inhibitor-1 Expression
title_fullStr Vehicle-dependent Effects of Sphingosine 1-phosphate on Plasminogen Activator Inhibitor-1 Expression
title_full_unstemmed Vehicle-dependent Effects of Sphingosine 1-phosphate on Plasminogen Activator Inhibitor-1 Expression
title_short Vehicle-dependent Effects of Sphingosine 1-phosphate on Plasminogen Activator Inhibitor-1 Expression
title_sort vehicle-dependent effects of sphingosine 1-phosphate on plasminogen activator inhibitor-1 expression
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5587522/
https://www.ncbi.nlm.nih.gov/pubmed/28321011
http://dx.doi.org/10.5551/jat.37663
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