Pujianto Dwi Ari, Permatasari Silvani
Department of Biology, Faculty of Medicine, Universitas Indonesia, Palangka Raya, Indonesia.
Department of Biology, Faculty of Medicine, Universitas Palangka Raya, Palangka Raya, Indonesia.
J Hum Reprod Sci. 2021 Oct-Dec;14(4):350-355. doi: 10.4103/jhrs.jhrs_29_21. Epub 2021 Dec 31.
Sperm maturation takes place through contact between sperm and proteins produced in the epididymal lumen. CD52 had been characterised in the sperm; however, the expression and its regulation in the epididymis are mostly unknown.
This study aimed to analyse the expression and regulation of CD52 in the mouse epididymis.
Experimental design was used in this study.
Epididymis tissues from mice strain Deutch Democratic Yokohama were used as sources of total RNA. Bioinformatic tool was used to predict signal peptides. Quantitative real-time reverse transcription-polymerase chain reaction was used to analyse tissue distribution, androgen, testicular factors dependency and postnatal development.
One-way analysis of variance was used to analyse differences between treatment and control untreated group. < 0.05 was determined as a significant difference.
CD52 amino acid sequence contains a signal peptide, indicating it is a secretory protein. CD52 exhibited region-specific expression in the epididymis, with the highest level being in the cauda. CD52 expression was regulated by androgen indicated by a significant downregulation at day 1 and day 3 following a castration ( < 0.05). Dependency on androgen was confirmed by injection of exogenous testosterone which prevented downregulation by 50%. Moreover, lumicrine factors also influenced CD52 expression indicated by ligation of efferent duct which also reduced expression at day 1 to day 5 following the ligation ( < 0.05). CD52 expression was developmentally regulated. This was shown by increase in the level of expression starting at day 15 postnatally.
CD52 shows characteristics of genes involved in sperm maturation in the epididymis.
精子成熟通过精子与附睾管腔中产生的蛋白质接触而发生。CD52已在精子中得到表征;然而,其在附睾中的表达及其调控情况大多未知。
本研究旨在分析CD52在小鼠附睾中的表达及调控。
本研究采用实验设计。
以德国民主横滨小鼠品系的附睾组织作为总RNA来源。使用生物信息学工具预测信号肽。采用定量实时逆转录聚合酶链反应分析组织分布、雄激素、睾丸因子依赖性及出生后发育情况。
采用单因素方差分析分析处理组与未处理对照组之间的差异。P < 0.05被确定为有显著差异。
CD52氨基酸序列包含一个信号肽,表明它是一种分泌蛋白。CD52在附睾中呈现区域特异性表达,在附睾尾部水平最高。去势后第1天和第3天CD52表达显著下调,表明其表达受雄激素调控(P < 0.05)。注射外源性睾酮可防止下调50%,从而证实了对雄激素的依赖性。此外,结扎输出小管后CD52表达也受到影响,结扎后第1天至第5天表达也降低,表明管腔分泌因子也影响CD52表达(P < 0.05)。CD52表达受发育调控。这表现为出生后第15天开始表达水平增加。
CD52显示出附睾中参与精子成熟的基因特征。