Hadjkacem-Loukil Lobna, Hadj-Kacem Hassen, Hadj Salem Ikhlass, Bahloul Ali, Fakhfakh Faiza, Ayadi Hammadi
Laboratory of Human Molecular Genetics, Faculty of Medicine, Sfax, Tunisia Unité Cibles pour le Diagnostic et la Thérapie, Centre de Biotechnologie de Sfax, Sfax, Tunisia Unit of research US 17, CHU Hospital Habib Bourguiba, Sfax, Tunisia.
Andrologia. 2011 Jul 6. doi: 10.1111/j.1439-0272.2010.01088.x.
Azoospermia factor (AZF) deletions were associated with severe oligospermia and azoospermia with testicular histologies varying from maturation arrest (MA) to Sertoli cell-only (SCO) phenotypes. Abnormal androgen receptor (AR) structure or function has also been implicated in male infertility. To assess the contribution of these genetic defects to azoospermic patients, 19 Tunisian men with SCO (n = 13) or MA (n = 6) were enrolled in this study. Using immunohistochemistry method, we evaluated the expression of AR in testicular biopsy for the two phenotypes. PCR with primers flanking the AR-(CAG)n region and direct sequencing were used to determine AR-(CAG)n length. And PCR amplification of 14 sequence-tagged sites (STSs) located at Yq was used to determine the rate and extent of Y microdeletions. We found a significant difference of the AR expression between SCO and MA cases. Hence, this expression in the testis depends on the status of spermatogenesis. However, we did not find any relationship between the (CAG) repeat and the testicular histology (neither for SCO nor MA). On the other hand, we found a high frequency of AZF deletions (46.2%) in SCOS and in MA (50%). The present results also suggest the contribution of Y chromosome microdeletions in SCO and MA pathogenesis.
无精子症因子(AZF)缺失与严重少精子症和无精子症相关,睾丸组织学表现从成熟停滞(MA)到唯支持细胞(SCO) phenotype不等。雄激素受体(AR)结构或功能异常也与男性不育有关。为了评估这些基因缺陷对无精子症患者的影响,本研究纳入了19名患有SCO(n = 13)或MA(n = 6)的突尼斯男性。使用免疫组织化学方法,我们评估了两种表型的睾丸活检中AR的表达。使用侧翼为AR-(CAG)n区域的引物进行PCR和直接测序来确定AR-(CAG)n的长度。并且使用位于Yq的14个序列标签位点(STS)的PCR扩增来确定Y微缺失的发生率和程度。我们发现SCO和MA病例之间AR表达存在显著差异。因此,睾丸中的这种表达取决于精子发生的状态。然而,我们没有发现(CAG)重复与睾丸组织学之间存在任何关系(无论是SCO还是MA)。另一方面,我们发现在SCOS和MA中AZF缺失的频率很高(分别为46.2%和50%)。目前的结果还表明Y染色体微缺失在SCO和MA发病机制中的作用。