Rich K A, Bardin C W, Gunsalus G L, Mather J P
Endocrinology. 1983 Dec;113(6):2284-93. doi: 10.1210/endo-113-6-2284.
The pattern and hormonal control of rat androgen-binding protein (rABP) secretion in vitro was investigated using animals of different ages to initiate primary cultures of Sertoli cells. Sertoli cells were isolated from testes of 7- to 31-day-old rats and cultured for periods of up to 30 days in serum-free medium, medium supplemented with insulin, transferrin, and epidermal growth factor (3F), or 3F plus FSH, testosterone, progesterone, hydrocortisone, and vitamin E (8F). The amount of rABP secreted by Sertoli cells during the first 24 h in culture (initial rate) exhibited an age-dependent pattern which reflected the apparent in vivo activity of these cells. Between 7 and 25 days of age, the initial rate of rABP secretion per Sertoli cell increased 20-fold; a further 2-fold increase occurred between 25 and 35 days of age. The pattern of rABP secretion exhibited by Sertoli cells cultured for several weeks was dependent not only on added factors (3F or 8F), but also on Sertoli cell age, expressed as the total of animal age plus time in culture (total age). In cultures of Sertoli cells isolated from very young animals (7-10 days old), the rate of rABP secretion increased until 20 days (total age), but declined thereafter. This early increase in rABP secretion was augmented by, but not dependent on, hormone additions. In contrast, Sertoli cells isolated from older animals always showed decreasing rates of secretion with time in culture. Furthermore, Sertoli cells from very young animals retained the capacity to respond to hormones in vitro with increased secretion of rABP and maintenance of cell viability. This responsiveness decreased with age, similar to the loss of hormone response seen in vivo after puberty. In conclusion, culture conditions were established which permitted the study of FSH-dependent and independent regulation of rABP secretion and of the acquisition of hormone resistance at the time of puberty. The initial rate of rABP secretion in culture (first 24 h) correlates with the age of the animal from which the cultures are obtained. The pattern of rABP secretion during subsequent long term culture is determined by the total age (animal and culture age), with increasing rates of secretion up to 20 days and decreasing rates thereafter. This inherent pattern of rABP secretion as well as loss of responsiveness of the Sertoli cell to hormonal stimulation appear to be programmed early in development.
利用不同年龄的动物启动支持细胞原代培养,研究了大鼠雄激素结合蛋白(rABP)体外分泌的模式和激素调控。从7至31日龄大鼠的睾丸中分离出支持细胞,并在无血清培养基、补充胰岛素、转铁蛋白和表皮生长因子(3F)的培养基或3F加促卵泡激素(FSH)、睾酮、孕酮、氢化可的松和维生素E(8F)的培养基中培养长达30天。支持细胞在培养的最初24小时(初始速率)分泌的rABP量呈现出一种年龄依赖性模式,这反映了这些细胞在体内的表观活性。在7至25日龄之间,每个支持细胞的rABP初始分泌速率增加了20倍;在25至35日龄之间又增加了2倍。培养数周的支持细胞所表现出的rABP分泌模式不仅取决于添加的因子(3F或8F),还取决于支持细胞的年龄,以动物年龄加上培养时间的总和(总年龄)表示。在从非常年幼的动物(7至10日龄)分离的支持细胞培养物中,rABP分泌速率在20天(总年龄)之前增加,但此后下降。rABP分泌的这种早期增加因添加激素而增强,但不依赖于激素添加。相反,从年长动物分离的支持细胞在培养过程中总是显示出分泌速率随时间下降。此外,来自非常年幼动物的支持细胞在体外仍保留对激素作出反应的能力,即rABP分泌增加且细胞活力维持。这种反应性随年龄下降,类似于青春期后在体内观察到的激素反应丧失。总之,建立了培养条件,从而能够研究rABP分泌的FSH依赖性和非依赖性调控以及青春期时激素抗性的获得。培养物中rABP的初始分泌速率(最初24小时)与获取培养物的动物年龄相关。随后长期培养期间的rABP分泌模式由总年龄(动物年龄和培养年龄)决定,分泌速率在20天之前增加,此后下降。rABP分泌的这种固有模式以及支持细胞对激素刺激反应性的丧失似乎在发育早期就已编程。