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性成熟过程中以及去势后睾酮处理时,小鼠睾丸和附睾中L-前列腺素D合成酶的表达与调控

L-prostaglandin D synthase expression and regulation in mouse testis and epididymis during sexual maturation and testosterone treatment after castration.

作者信息

Zhu Hui, Ma Hong, Ni Hua, Ma Xing-Hong, Mills Nathaniel, Yang Zeng-Ming

机构信息

College of Life Sciences, Northeast Agricultural University, Harbin 150030, China.

出版信息

Endocrine. 2004 Jun;24(1):39-45. doi: 10.1385/ENDO:24:1:039.

Abstract

Lipocalin-type prostaglandin D synthase (L-PGDS) is highly expressed in the adult testis and epididymis of many mammals. The present study was to investigate L-PGDS expression in mouse testis and epididymis during sexual maturation, and the effects of testosterone replacement on L-PGDS expression in epididymis by in situ hybridization and immunohistochemistry. Both L-PGDS mRNA and protein were highly expressed in the interstitial tissue of adult testis. L-PGDS mRNA was first detected on d 30 after birth and exhibited an abundant signal in adult caput and cauda epididymis. L-PGDS immunostaining was first observed on d 30 after birth. There was a strong level of L-PGDS immunostaining in adult epididymis. Castrated male mice were treated with either vehicle or testosterone propionate following 3 d postcastration. L-PGDS expression steadily declined in a time-dependent fashion in control groups. No L-PGDS mRNA expression or immunostaining was detected in the controls for 12 d. When the castrated mice were treated with testosterone propionate for 5 or 12 d, L-PGDS expression was significantly increased in the whole epididymis. These data suggest that L-PGDS expression in mouse epididymis gradually declined in parallel to the declining concentration of endogenous androgen after castration and increased with the treatment of exogenous testosterone, indicating that L-PGDS expression in mouse epididymis was modulated by androgen levels. However, differential expression in different areas of the epididymis may also be influenced by factors derived from the testis.

摘要

脂联素型前列腺素D合成酶(L-PGDS)在许多哺乳动物的成年睾丸和附睾中高表达。本研究旨在通过原位杂交和免疫组织化学方法,研究性成熟过程中小鼠睾丸和附睾中L-PGDS的表达情况,以及睾酮替代对附睾中L-PGDS表达的影响。L-PGDS mRNA和蛋白在成年睾丸的间质组织中均高表达。L-PGDS mRNA在出生后第30天首次被检测到,在成年附睾头和附睾尾中呈现丰富的信号。L-PGDS免疫染色在出生后第30天首次观察到。成年附睾中有较强水平的L-PGDS免疫染色。去势雄性小鼠在去势后3天,分别用溶剂或丙酸睾酮处理。对照组中L-PGDS表达呈时间依赖性稳步下降。在12天内,对照组中未检测到L-PGDS mRNA表达或免疫染色。当去势小鼠用丙酸睾酮处理5天或12天时,整个附睾中L-PGDS表达显著增加。这些数据表明,去势后小鼠附睾中L-PGDS表达随着内源性雄激素浓度的下降而逐渐降低,而外源性睾酮处理则使其表达增加,这表明小鼠附睾中L-PGDS表达受雄激素水平调节。然而,附睾不同区域的差异表达也可能受来自睾丸的因素影响。

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