Zarnescu Otilia
Department of Animal Biology, Faculty of Biology, University of Bucharest, Splaiul Independentei 91-95, Bucharest-5, Romania.
Cell Tissue Res. 2007 May;328(2):401-10. doi: 10.1007/s00441-006-0373-3. Epub 2007 Jan 25.
The acetylation of core histones has been correlated with the deposition of free histones onto newly replicated DNA, transcriptional activity and the displacement of histones by protamines during spermiogenesis. The aim of the present study was to investigate the immunohistochemical distribution of hyperacetylated H4 during spermatogenesis in Polyodon spathula and to correlate these findings with the pattern of chromatin condensation in spermatids. In immature testis, the Sertoli cells showed more intense immunoreactivity for highly acetylated H4 than that of most primary spermatogonia. The testis of paddlefish at the beginning of spermatogenesis possessed early secondary spermatogonia and late secondary spermatogonia/preleptotene primary spermatocyte with intense nuclear immunoreactivity for highly acetylated H4. In seminiferous tubules in which secondary spermatogonia nuclei were intensely immunostained, Sertoli cell nuclei were unstained. Testes in late spermatogenesis contained tubules in which the immunohistochemical reaction for highly acetylated H4 was positive in the nuclei of preleptotene primary spermatocytes and secondary spermatocytes and in spermatids at the beginning of the elongation process. No immunostaining was found in round spermatids and spermatozoa. During the resting stage, immunostaining was confined to the nuclei of spermatogonia and the cells from the interstitial tissue. Transmission electron microscopy revealed that early spermatids had a round nucleus with filaments of fine chromatin that were dispersed or condensed in clumps. In later stages of maturation, the spermatids had slightly oval nuclei and homogeneous granular chromatin. The chromatin of advanced spermatids was organized into thick fibres. At the end of spermiogenesis, spermatozoan nuclei consisted of homogeneous highly compacted chromatin.
核心组蛋白的乙酰化与游离组蛋白在新复制DNA上的沉积、转录活性以及精子发生过程中鱼精蛋白取代组蛋白有关。本研究的目的是调查匙吻鲟精子发生过程中高乙酰化H4的免疫组织化学分布,并将这些发现与精子细胞中染色质浓缩模式相关联。在未成熟睾丸中,支持细胞对高乙酰化H4的免疫反应性比大多数初级精原细胞更强。精子发生开始时匙吻鲟的睾丸含有早期次级精原细胞和晚期次级精原细胞/前细线期初级精母细胞,其细胞核对高乙酰化H4有强烈的免疫反应性。在次级精原细胞核被强烈免疫染色的生精小管中,支持细胞核未被染色。精子发生后期的睾丸含有一些小管,其中高乙酰化H4的免疫组织化学反应在前期初级精母细胞和次级精母细胞以及伸长过程开始时的精子细胞的细胞核中呈阳性。圆形精子细胞和精子中未发现免疫染色。在静止期,免疫染色局限于精原细胞核和间质组织细胞。透射电子显微镜显示,早期精子细胞有一个圆形细胞核,其中细染色质丝分散或聚集成团。在成熟后期,精子细胞有略呈椭圆形的细胞核和均匀的颗粒状染色质。晚期精子细胞的染色质组织成粗纤维。在精子发生结束时,精子细胞核由均匀高度压缩的染色质组成。