首页> 外文期刊>Journal of Anatomy >Transforming growth factor-beta 2 heterozygous mutant mice exhibit Cowper's gland hyperplasia and cystic dilations of the gland ducts (Cowper's syringoceles).
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Transforming growth factor-beta 2 heterozygous mutant mice exhibit Cowper's gland hyperplasia and cystic dilations of the gland ducts (Cowper's syringoceles).

机译:转化生长因子-β2杂合突变小鼠表现出考珀氏腺增生和腺管的囊性扩张(考珀氏囊突)。

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Analyses of mutant mice with a deletion for the transforming growth factor beta 2 (Tgfbeta2) gene revealed cysts in the perineal/scrotal region of male mice. We present evidence from in situ, light and electron microscopy that the cysts observed in Tgfbeta2+/- heterozygous mice males derive from Cowper's gland tissue. The Cowper's glands of Tgfbeta2+/- heterozygous mutant mice display all steps of glandular hyperplasia and cystic dilation. TGF-beta isoforms and TGF-beta receptor (TbetaR-II) were localized immunocytochemically in sections of Cowper's glands. TGF-beta2 and TGF-beta3 were located predominantly in myoepithelial cells of the Cowper's gland whereas the TbetaRII was found in the plasma membrane of the acinar cells. TUNEL-assays revealed that apoptotic cell death is significantly reduced in Cowper's glands of TgfbetaB2+/- heterozygous mutant mice. The fact that Tgfbeta2+/- heterozygous mutant mice exhibit hyperplasia of Cowper's gland epithelium and Cowper's gland cysts suggests a disturbance of epithelial-stromal interaction most likely due to reduced TGF-beta2 level, accompanied by a significant decrease in apoptosis.
机译:突变小鼠的转化生长因子β2(Tgfbeta2)基因缺失的分析显示在雄性小鼠的会阴/阴囊区域有囊肿。我们提供了从原位,光和电子显微镜观察到的证据,即在雄性Tgfbeta2 +/-杂合小鼠中观察到的囊肿来自考珀氏腺组织。 Tgfbeta2 +/-杂合突变小鼠的考珀氏腺表现出腺体增生和囊性扩张的所有步骤。 TGF-β亚型和TGF-β受体(TbetaR-II)免疫细胞化学定位在考珀氏腺的切片中。 TGF-beta2和TGF-beta3主要位于考珀氏腺的肌上皮细胞中,而TbetaRII位于腺泡细胞的质膜中。 TUNEL分析显示,在TgfbetaB2 +/-杂合突变小鼠的考珀氏腺中,凋亡细胞的死亡明显减少。 Tgfbeta2 +/-杂合突变小鼠表现出考珀氏腺上皮和考珀氏囊肿的增生这一事实表明,上皮-基质相互作用的紊乱很可能是由于TGF-beta2水平降低,并伴随着凋亡的显着减少。

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