Reduced Morg1 expression in ischemic human brain

被引:8
作者
Haase, Daniela [2 ]
Keiner, Silke [3 ]
Mawrin, Christian [1 ,2 ]
Wolf, Gunter [4 ]
机构
[1] Otto VonGuericke Univ Magdegurg, Dept Neuropathol, D-39120 Magdeburg, Germany
[2] Univ Jena, Dept Neuropathol, D-6900 Jena, Germany
[3] Univ Jena, Dept Neurol, D-6900 Jena, Germany
[4] Univ Jena, Dept Internal Med 3, D-6900 Jena, Germany
关键词
Morg1; Brain; Ischemia; HIF-1; HYPOXIA-INDUCIBLE FACTOR-1-ALPHA; PROLYL HYDROXYLASE INHIBITORS; CELL-DEATH; FACTOR-I; APOPTOSIS; SCAFFOLD; PROTEIN; TARGET; GENES;
D O I
10.1016/j.neulet.2009.03.048
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
The mitogen-activated protein kinase organizer 1 (Morg1) has been recently identified as modular scaffold regulating ERK signaling. Morg1 also attenuates expression of the hypoxia-inducible factor-1 alpha (HIF-1 alpha) by activating or stabilizing of prolyl-hydroxylase 3 (PHD3). Here we demonstrate for the first time that Morg1 is expressed in the human brain in neurons, glial cells, and blood vessel walls. Immunohistochemistry, RT real-time PCR and western blotting indicated that Morg1 expression is reduced in human brain tissue with ischemic damage. Moreover, reactive astrocytes in the surrounding brain tissue showed strong Morg1 expression. Since hypoxic adaptation with enhancing HIF-1 alpha expression can engage a genetic program leading to profound sparing of brain tissue and enhanced recovery of function, down-regulation of Morg1 expression in the ischemic brain may be viewed as an intrinsic mechanism to stimulate this response. On the other hand, upregulation of Morg1 in astrocytes surrounding the penumbra may counteract this hypoxic adaptation. (C) 2009 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:46 / 50
页数:5
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