Gerard A, Nya A E, Egloff M, Domingo M, Degrelle H, Gerard H
Laboratoire d'Histologie-Embryologie II, Faculté de Médecine de Nancy I, France.
Ann N Y Acad Sci. 1991;637:258-76. doi: 10.1111/j.1749-6632.1991.tb27314.x.
We investigate in this study the hypothesis of human sex steroid-binding protein hSBP internalization into germ cells in a primate model. Human SBP was purified from late-pregnancy serum and labeled either with colloidal gold particles (18 nm) or with [3H]delta 6-testosterone by photoaffinity treatment. The germ cells were isolated from sexually mature monkey testis or caput epididymis (Macaca fascicularis) by mechanical means and cell suspensions (4 x 10(6) per 100 microliters culture medium) were incubated in presence of hSBP-gold complex (60 ng/100 microliters) or hSBP-[3H]delta 6-testosterone complex (66 ng/100 microliters, 20,000 cpm) for 2, 5, 15, 45, and 60 min. The samples were processed for electron microscopy followed by autoradiographic treatment for the radiolabeled samples. Localization of the label occurred over the whole germ cell lineage whichever tracer was used. Spermatogonia, spermatocytes, spermatids, testicular and epididymal spermatozoa exhibited specific binding sites over the plasma membrane associated with clathrin-like coated pits and vesicles. At 34 degrees C, intracellular localization of the labeled ligand was found within coated vesicles, in early and late endosomes. In addition, in early spermatogenic cells, labeled ligand was detected in the nuclei and/or associated with the nuclear envelope whereas in late spermatids and residual bodies, the labeling was accumulated in multivesicular, prelysosomal structures. Quantitative analysis of the "labeled cells/total cells" ratio exhibited a negative correlation to the maturation steps, epididymal spermatozoa being the least labeled. The cellular distribution is similar with one or the other protein in the same spermatogenic cells. Unlabeled hSBP treatment prior to labeled hSBP reduced significantly the internalization. Lowering the temperature to 4 degrees C prevented endocytosis and enhanced membrane binding. EDTA pretreatment strongly decreased hSBP internalization and modified the early endocytic steps, namely, the pinching off of the coated vesicles. It is concluded that monkey germ cells are able to internalize the human sex steroid-binding protein through specific endocytic organelles. This endocytosis leads to the labeling of the nuclei in the early spermatogenic cells and of the multivesicular bodies in the late germ cells. This strongly suggests that steroid-binding proteins may be required for spermatogenesis in acting at the germ cell lineage level either by themselves or by serving as steroid transmembrane carriers.
在本研究中,我们在灵长类动物模型中研究了人类性类固醇结合蛋白hSBP内化进入生殖细胞的假说。从妊娠晚期血清中纯化人SBP,并通过光亲和处理用胶体金颗粒(18纳米)或[3H]δ6-睾酮进行标记。通过机械方法从性成熟的猴睾丸或附睾头部(食蟹猴)分离出生殖细胞,并将细胞悬液(每100微升培养基中含4×10⁶个细胞)在hSBP-金复合物(60纳克/100微升)或hSBP-[3H]δ6-睾酮复合物(66纳克/100微升,20,000计数/分钟)存在的情况下孵育2、5、15、45和60分钟。对样品进行电子显微镜处理,然后对放射性标记的样品进行放射自显影处理。无论使用哪种示踪剂,标记都出现在整个生殖细胞谱系上。精原细胞、精母细胞、精子细胞、睾丸和附睾精子在与网格蛋白样包被小窝和小泡相关的质膜上表现出特异性结合位点。在34℃时,在包被小泡、早期和晚期内体中发现标记配体的细胞内定位。此外,在早期生精细胞中,在细胞核内和/或与核膜相关处检测到标记配体,而在晚期精子细胞和残余小体中,标记物积聚在多囊泡、前溶酶体结构中。“标记细胞/总细胞”比率的定量分析显示与成熟步骤呈负相关,附睾精子的标记最少。在相同的生精细胞中,一种或另一种蛋白质的细胞分布相似。在用标记的hSBP处理之前用未标记的hSBP处理可显著降低内化。将温度降至4℃可防止内吞作用并增强膜结合。EDTA预处理强烈降低hSBP内化并改变早期内吞步骤,即包被小泡的缢断。结论是猴生殖细胞能够通过特定的内吞细胞器内化人类性类固醇结合蛋白。这种内吞作用导致早期生精细胞中的细胞核和晚期生殖细胞中的多囊泡体被标记。这强烈表明类固醇结合蛋白可能是精子发生所必需的,它们可能通过自身作用或作为类固醇跨膜载体在生殖细胞谱系水平发挥作用。