Distribution of Corticosteroid Receptors in Mature Oligodendrocytes and Oligodendrocyte Progenitors of the Adult Mouse Brain

被引:49
作者
Matsusue, Yumiko [1 ,2 ]
Horii-Hayashi, Noriko [2 ]
Kirita, Tadaaki [1 ]
Nishi, Mayumi [2 ]
机构
[1] Nara Med Univ, Dept Oral & Maxillofacial Surg, Kashihara, Nara 6348521, Japan
[2] Nara Med Univ, Dept Anat & Cell Biol, Kashihara, Nara 6348521, Japan
基金
日本学术振兴会;
关键词
corticosteroid (glucocorticoid); Glucocorticoid receptor; mineralocorticoid receptor; oligodendrocyte progenitor; oligodendrocyte; cofactor; CENTRAL-NERVOUS-SYSTEM; GLUCOCORTICOID-RECEPTOR; SCHWANN-CELLS; MINERALOCORTICOID RECEPTOR; NG2; PROTEOGLYCAN; SPINAL-CORD; MULTIPLE-SCLEROSIS; P160; COACTIVATORS; GLIAL-CELLS; ASTROCYTES;
D O I
10.1369/0022155413517700
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
The expression of glucocorticoid receptors (GRs) was investigated immunohistochemically in two different lineages of oligodendrocytes, using carbonic anhydrase (CA) II and neuron glial antigen (NG) 2 as markers of mature oligodendrocytes and oligodendrocyte progenitors, respectively. We focused on the gray matter regions, including CA1, CA3 and the dentate gyrus of the hippocampus, the primary somatosensory cortex barrel field and the basolateral amygdala, and the white matter regions, including the corpus callosum, external capsule and fimbria of the hippocampus. More than 80% of CAII-immunoreactive (IR) cells and more than 95% of NG2-IR cells expressed GRs in various regions of the brain. In contrast, neither CAII-IR cells nor NG2-IR cells expressed mineralocorticoid receptors (MRs) in the same regions. The intensity of GR expression was drastically reduced in CA II-IR cells and NG2-IR cells in the same regions in adrenalectomized mice. Finally, steroid receptor co-activator (SRC)-1 and p300, both of which are cofactors for GR, were expressed in the gray and white matter regions in NG2-IR cells, but not in CAII-IR cells. These results suggest that the expression of GRs in oligodendrocytes and their progenitor cells mediates several functions in vivo, including differentiation and myelination, as a major target of glucocorticoids and their cofactors.
引用
收藏
页码:211 / 226
页数:16
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