首页> 外文期刊>Acta histochemica et cytochemica. >Compensatory Upregulation of Myelin Protein Zero-Like 2 Expression in Spermatogenic Cells in Cell Adhesion Molecule-1-Deficient Mice
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Compensatory Upregulation of Myelin Protein Zero-Like 2 Expression in Spermatogenic Cells in Cell Adhesion Molecule-1-Deficient Mice

机译:细胞粘附分子-1缺陷小鼠生精细胞中髓磷脂蛋白零样2表达的补偿性上调。

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The cell adhesion molecule-1 (Cadm1) is a member of the immunoglobulin superfamily. In the mouse testis, Cadm1 is expressed in the earlier spermatogenic cells up to early pachytene spermatocytes and also in elongated spermatids, but not in Sertoli cells. Cadm1-deficient mice have male infertility due to defective spermatogenesis, in which detachment of spermatids is prominent while spermatocytes appear intact. To elucidate the molecular mechanisms of the impaired spermatogenesis caused by Cadm1 deficiency, we performed DNA microarray analysis of global gene expression in the testis compared between Cadm1-deficient and wild-type mice. Out of the 25 genes upregulated in Cadm1-deficient mice, we took a special interest in myelin protein zero-like 2 (Mpzl2), another cell adhesion molecule of the immunoglobulin superfamily. The levels of Mpzl2 mRNA increased by 20-fold and those of Mpzl2 protein increased by 2-fold in the testis of Cadm1-deficient mice, as analyzed with quantitative PCR and western blotting, respectively. In situ hybridization and immunohistochemistry demonstrated that Mpzl2 mRNA and protein are localized in the earlier spermatogenic cells but not in elongated spermatids or Sertoli cells, in both wild-type and Cadm1-deficient mice. These results suggested that Mpzl2 can compensate for the deficiency of Cadm1 in the earlier spermatogenic cells.
机译:细胞粘附分子-1(Cadm1)是免疫球蛋白超家族的成员。在小鼠的睾丸中,Cadm1在早期的生精细胞中直至早期的粗线精原细胞中都表达,在细长的精子细胞中也表达,但在Sertoli细胞中不表达。 Cadm1缺陷型小鼠由于精子发生缺陷而具有雄性不育,其中精子脱离明显,而精细胞则完整。为了阐明由Cadm1缺乏引起的精子发生受损的分子机制,我们比较了缺乏Cadm1的小鼠和野生型小鼠的睾丸中整体基因表达的DNA微阵列分析。在缺乏Cadm1的小鼠中上调的25个基因中,我们对髓磷脂蛋白零样2(Mpzl2)(免疫球蛋白超家族的另一个细胞粘附分子)特别感兴趣。在Cadm1缺陷小鼠的睾丸中,Mpzl2 mRNA的水平增加了20倍,Mpzl2蛋白的水平增加了2倍,分别通过定量PCR和Western印迹分析。原位杂交和免疫组织化学表明,在野生型和Cadm1缺陷型小鼠中,Mpzl2 mRNA和蛋白都位于较早的生精细胞中,而不在伸长的精子细胞或支持细胞中。这些结果表明,Mpzl2可以弥补早期生精细胞中Cadm1的缺乏。

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