Fentener van Vlissingen J M, van Zoelen E J, Ursem P J, Wensing C J
Department of Veterinary Anatomy, State University Utrecht, The Netherlands.
Endocrinology. 1988 Dec;123(6):2868-77. doi: 10.1210/endo-123-6-2868.
The gubernaculum testis is the connective tissue organ that causes the testis to descend. How the process of testicular descent is regulated is not fully understood. Current hypotheses postulate that a nonandrogenic fetal testicular factor controls the first phase of descent, that is characterized by growth of the gubernaculum and transabdominal migration of the testis. When gonadal extracts from fetuses with ages corresponding to the first phase of testicular descent (50, 60, and 75 days) were tested on gubernacular cells, the growth stimulatory effect of testicular extracts exceeded the effect of both ovarian extract and fetal calf serum. Gonadal extracts from 80-, 90-, and 100-day-old fetuses showed only a minor sex difference. No sex difference or age-dependent changes were detected when fetal gonadal extracts were tested on murine 3T3 cells. Polypeptide growth factors (epidermal growth factor, insulin, fibroblast growth factor, platelet-derived growth factor, and transforming growth factor-beta) were tested for growth stimulatory activity and had only minor effects on gubernaculum cells. Fetal testicular hormones (anti-Müllerian hormone, inhibin, and androgenic steroids) did not induce initiation of DNA synthesis at concentrations that are highly bioactive in typical target systems. When testicular samples were dialyzed, the high mol wt fraction (greater than 3500) had lower growth stimulatory activity in gubernaculum cells, but not 3T3 cells. Bioactivity of ovarian extracts and fetal calf serum was not diminished after dialysis. The low mol wt fraction (less than 3500) of testicular extract was distinctly stimulatory to gubernaculum cells but not 3T3 cells, and the low mol wt fraction of ovarian extracts did not stimulate growth in either cell type. It was concluded that the fetal porcine testis during the first phase of testicular descent contains low mol wt factor(s) to which gubernaculum cells and not 3T3 cells are responsive. The bioactive fraction probably contains the factor(s) that initiate testicular descent. We suggest the name descendin for this new activity.
睾丸引带是促使睾丸下降的结缔组织器官。睾丸下降过程是如何调控的尚未完全明确。目前的假说认为,一种非雄激素性的胎儿睾丸因子控制着下降的第一阶段,该阶段的特征是睾丸引带生长以及睾丸经腹迁移。当用对应睾丸下降第一阶段(50、60和75天)胎儿的性腺提取物对睾丸引带细胞进行检测时,睾丸提取物的生长刺激作用超过了卵巢提取物和胎牛血清的作用。80、90和100日龄胎儿的性腺提取物仅显示出微小的性别差异。当用胎儿性腺提取物对小鼠3T3细胞进行检测时,未检测到性别差异或年龄依赖性变化。对多肽生长因子(表皮生长因子、胰岛素、成纤维细胞生长因子、血小板衍生生长因子和转化生长因子-β)的生长刺激活性进行了检测,它们对睾丸引带细胞仅有微小作用。胎儿睾丸激素(抗苗勒管激素、抑制素和雄激素类固醇)在典型靶系统中具有高生物活性的浓度下,并未诱导DNA合成的起始。当对睾丸样本进行透析时,高分子量部分(大于3500)对睾丸引带细胞的生长刺激活性较低,但对3T3细胞则不然。透析后卵巢提取物和胎牛血清的生物活性并未降低。睾丸提取物的低分子量部分(小于3500)对睾丸引带细胞有明显的刺激作用,但对3T3细胞无此作用,而卵巢提取物的低分子量部分对两种细胞类型的生长均无刺激作用。得出的结论是,睾丸下降第一阶段的胎儿猪睾丸含有低分子量因子,睾丸引带细胞对其有反应,而3T3细胞则无反应。这种生物活性部分可能含有启动睾丸下降的因子。我们建议将这种新活性命名为降睾素。