Oko R, Hermo L, Hecht N B
Department of Anatomy, McGill University, Montreal, Canada.
Anat Rec. 1991 Sep;231(1):63-81. doi: 10.1002/ar.1092310108.
Recently, a cDNA that coded for an enteric smooth muscle gamma-actin (SMGA) that was expressed in post-meiotic mouse testicular cells was identified. To determine the cellular location(s) of the protein encoded by this cDNA, this SMGA was probed for by immunocytochemistry in the cells of the seminiferous epithelium with two different monoclonal antibodies (Mabs), B4 and HUC 1-1, known to be muscle actin selective. As a control, we also examined the immunoreactivity of a third Mab, C4, that reacts with all non-muscle and muscle vertebrate isoactins. Using light and electron microscopy, a progressive increase in immunolabeling was observed with the muscle selective HUC 1-1 Mab over a loose actin filamentous network distributed throughout the cytoplasm of steps 4-16 spermatids. Thereafter, the labeling decreased such that at step 17 spermatids, only cytoplasmic labeling in the tail of the spermatids was observed. No labeling of this network was noted with the C4 or B4 Mabs. However, myoid cells enveloping seminiferous tubules and smooth muscle cells of interstitial blood vessels demonstrated comparable intense labeling with each of the three Mabs. The C4 Mab intensely labeled actin filaments of the Sertoli-Sertoli and Sertoli-spermatid ectoplasmic specializations. Also well labeled were numerous actin filaments found in the apical Sertoli cell processes encapsulating the heads of late step 19 spermatids at stage VII of the cycle of the seminiferous epithelium. In addition, actin filamentous bundles enveloping tubulobulbar complexes of the late spermatids within the Sertoli cell apical processes were intensely labeled. The actin filaments in the Sertoli apical processes and surrounding the tubulobulbar complexes were also strongly immunolabeled with the HUC 1-1 Mab. The C4 Mab but not the B4 or HUC 1-1 Mabs, recognized actin in the subacrosomal space of steps 4-18 spermatids. This study suggests that there are muscle isoforms of actin within the cytoplasm of developing spermatids and within apical processes of Sertoli cells.
最近,一种编码在减数分裂后小鼠睾丸细胞中表达的肠平滑肌γ-肌动蛋白(SMGA)的cDNA被鉴定出来。为了确定该cDNA编码的蛋白质的细胞定位,用两种已知对肌肉肌动蛋白具有选择性的不同单克隆抗体(Mab),即B4和HUC 1-1,通过免疫细胞化学方法在生精上皮细胞中检测这种SMGA。作为对照,我们还检测了第三种Mab,即C4的免疫反应性,它能与所有非肌肉和肌肉脊椎动物肌动蛋白异构体发生反应。利用光学显微镜和电子显微镜观察发现,在第4-16步精子细胞整个细胞质中分布的松散肌动蛋白丝网络上,肌肉选择性的HUC 1-1 Mab的免疫标记逐渐增加。此后,标记减少,以至于在第17步精子细胞时,仅在精子细胞尾部观察到细胞质标记。用C4或B4 Mab未观察到该网络的标记。然而,包绕生精小管的肌样细胞和间质血管的平滑肌细胞对这三种Mab中的每一种都表现出相当强烈的标记。C4 Mab强烈标记支持细胞-支持细胞和支持细胞-精子细胞外质特化结构中的肌动蛋白丝。在生精上皮周期VII期包绕第19步后期精子细胞头部的支持细胞顶端突起中发现的许多肌动蛋白丝也被很好地标记。此外,在支持细胞顶端突起内包绕后期精子细胞的管球复合体的肌动蛋白丝束也被强烈标记。支持细胞顶端突起中和围绕管球复合体的肌动蛋白丝也被HUC 1-1 Mab强烈免疫标记。C4 Mab能识别第4-18步精子细胞顶体下间隙中的肌动蛋白,而B4或HUC 1-1 Mab则不能。这项研究表明,在发育中的精子细胞细胞质和支持细胞顶端突起中存在肌动蛋白的肌肉异构体。