Hypoxia inhibits semicarbazide-sensitive amine oxidase activity in adipocytes

被引:7
|
作者
Repesse, Xavier [1 ,2 ]
Moldes, Marthe [3 ,4 ]
Muscat, Adeline [1 ,3 ,4 ]
Vatier, Camille [3 ,4 ,5 ]
Chetrite, Gerard [1 ,3 ,4 ,5 ]
Gille, Thomas [6 ,7 ]
Planes, Carole [6 ,7 ]
Filip, Anna [8 ]
Mercier, Nathalie [8 ,9 ]
Duranteau, Jacques [10 ,11 ]
Feve, Bruno [1 ,3 ,4 ,5 ]
机构
[1] Univ Paris 11, INSERM, UMR S 1185, Le Kremlin Bicetre, France
[2] Hop Ambroise Pare, AP HP, Pole Thorax Vaisseaux Abdomen Metabolisme, Serv Reanimat Med Chirurg, F-92104 Boulogne, France
[3] Univ Paris 06, Sorbonne Univ, Ctr Rech St Antoine, INSERM,UMR S 938, Paris, France
[4] Univ ICAN, Inst Hosp, Paris, France
[5] Hop St Antoine, AP HP, Serv Endocrinol, F-75571 Paris, France
[6] Univ Paris 13, Sorbonne Paris Cite, EA2363, Bobigny, France
[7] Hop Avicenne, AP HP, Serv Explorat Fonct, F-93009 Bobigny, France
[8] INSERM, U1116, Fac Med, Vandoeuvre Les Nancy, France
[9] Univ Lorraine, Nancy, France
[10] Hop Bicetre, AP HP, Serv Anesthesie Reanimat, Le Kremlin Bicetre, France
[11] Equipe Univ 3509, Microcirculat Bioenerget Inflammat & Insuffisance, Paris, France
关键词
Adipocyte; Hypoxia; Diabetes; Obesity; SSAO; DEPENDENT DIABETES-MELLITUS; ADIPOSE-TISSUE; INDUCIBLE FACTOR-1; TRANSGENIC MICE; CRITICALLY-ILL; EXPRESSION; OBESITY; DIFFERENTIATION; DEHYDROGENASE; CONSEQUENCES;
D O I
10.1016/j.mce.2015.04.011
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Semicarbazide-sensitive amine oxidase (SSAO), an enzyme highly expressed on adipocyte plasma membranes, converts primary amines into aldehydes, ammonium and hydrogen peroxide, and is likely involved in endothelial damage during the course of diabetes and obesity. We investigated whether in vitro, adipocyte SSAO was modulated under hypoxic conditions that is present in adipose tissue from obese or intensive care unit. Physical or pharmacological hypoxia decreased SSAO activity in murine adipocytes and human adipose tissue explants, while enzyme expression was preserved. This effect was time-, dose-dependent and reversible. This down-regulation was confirmed in vivo in subcutaneous adipose tissue from a rat model of hypoxia. Hypoxia-induced suppression in SSAO activity was independent of the HIF-1-alpha pathway or of oxidative stress, but was partially antagonized by medium acidification. Hypoxia-induced downregulation of SSAO activity could represent an adaptive mechanism to lower toxic molecules production, and may thus protect from tissue injury during these harmful conditions. (C) 2015 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:58 / 66
页数:9
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