Cigorraga S B, Chemes H, Pellizzari E
Centro de Investigaciones Endocrinológicas, Hospital de Niños R. Gutiérrez, Buenos Aires, Argentina.
Biol Reprod. 1994 Dec;51(6):1193-205. doi: 10.1095/biolreprod51.6.1193.
We have explored the morphogenic and functional characteristics of human peritubular cells originating from seminiferous tubule (ST) fragments isolated from the testes of two prepubertal patients with the androgen insensitivity syndrome. These ST were cultured in Dulbecco's Modified Eagle's Medium-Ham's F-12 supplemented with antibiotics, transferrin, hydrocortisone, vitamin E, and 3% fetal bovine serum. A centrifugal growth of elongated fibroblast-like cells peripheral to the ST explants was observed. Muscle-specific actin and 3 beta-hydroxysteroid dehydrogenase were evident in the peritubular area and in the elongated cells growing from the tubules. Histochemistry was negative in the tubules themselves, revealing the mixed nature of these cultures. The ST fragments were lost after subculturing, leaving a homogeneous monolayer of fibroblast-like cells. The steroidogenic potential of these cells was demonstrated by the secretion of testosterone (T) to the culture medium. T secretion was stimulated by hCG in a time-dependent fashion (patient 1: Day 11, 84% and Day 15, 200%; patient 2: Day 8, 73% and Day 11, 32% over basal). FSH also stimulated T secretion (patient 1: Day 5, 136% and Day 8, 89%; patient 2: Day 8, 117% and Day 11, 129% over basal). Furthermore, T secretion by these cultures was 100% higher than that observed in mesenchymal cells obtained from the testicular intertubular space in the same patient. Spontaneous T secretion and hormone responses declined progressively to cease by 25 days in culture. These results suggested the involvement of Sertoli cell (SC)-secreted factor(s) in the regulation of T secretion by peritubular cells. In order to further explore possible paracrine interactions between peritubular and Sertoli cells, we carried out heterologous cocultures with rat SC. After 72 h a striking redistribution of both cell types was observed with the formation of cord-like structures. Ultrastructural examination of these cords showed the formation of a basement membrane between epithelial (Sertoli) and mesenchymal cells of peritubular origin. No resumption of T secretion was observed, but an increase in androgen-binding protein (ABP) production by rat SC under basal (37%) and FSH-stimulated (52%) conditions was evident. Our results show that in the human peritubular compartment, cells exist that can alternatively express steroidogenic functions, associate with SC in a specific mesenchymal-epithelial interaction, and exert regulatory influences on ABP secretion by SC. In addition they indicate that communicating events in the testis are preserved throughout evolution.
我们研究了源自两名青春期前雄激素不敏感综合征患者睾丸中分离出的生精小管(ST)片段的人睾丸周细胞的形态发生和功能特征。这些ST在补充有抗生素、转铁蛋白、氢化可的松、维生素E和3%胎牛血清的杜氏改良 Eagle 培养基 - Ham's F - 12中培养。观察到ST外植体周围有细长的成纤维细胞样细胞呈离心生长。肌肉特异性肌动蛋白和3β - 羟基类固醇脱氢酶在睾丸周区域以及从小管生长出的细长细胞中明显可见。小管本身的组织化学检测为阴性,揭示了这些培养物的混合性质。传代培养后ST片段丢失,留下一层均匀的成纤维细胞样细胞单层。这些细胞的类固醇生成潜力通过向培养基中分泌睾酮(T)得以证明。hCG以时间依赖性方式刺激T分泌(患者1:第11天,增加84%;第15天,增加200%;患者2:第8天,增加73%;第11天,比基础水平增加32%)。FSH也刺激T分泌(患者1:第5天,增加136%;第8天,增加89%;患者2:第8天,增加117%;第11天,比基础水平增加129%)。此外,这些培养物分泌的T比同一患者睾丸间质空间获得的间充质细胞中观察到的高出100%。培养25天时,自发T分泌和激素反应逐渐下降直至停止。这些结果表明支持细胞(SC)分泌的因子参与调节睾丸周细胞的T分泌。为了进一步探索睾丸周细胞和支持细胞之间可能的旁分泌相互作用,我们与大鼠SC进行了异源共培养。72小时后,观察到两种细胞类型显著重新分布并形成索状结构。对这些索的超微结构检查显示,在上皮(支持)细胞和睾丸周来源的间充质细胞之间形成了基底膜。未观察到T分泌恢复,但在基础(增加37%)和FSH刺激(增加52%)条件下,大鼠SC产生的雄激素结合蛋白(ABP)明显增加。我们的结果表明,在人类睾丸周隔室中,存在能够交替表达类固醇生成功能、在特定的间充质 - 上皮相互作用中与支持细胞结合并对支持细胞的ABP分泌发挥调节作用的细胞。此外,它们表明睾丸中的通讯事件在整个进化过程中得以保留。