Canipari R, Galdieri M
Department of Histology and Medical Embryology, University of Rome La Sapienza, Rome, Italy.
Biol Reprod. 2000 Aug;63(2):544-50. doi: 10.1095/biolreprod63.2.544.
Tissue type (t) and urokinase type (u) plasminogen activators (PAs) have been shown to be secreted by Sertoli cells in the seminiferous tubules in a cyclic fashion and to be dependent upon FSH stimulation or upon the presence of adjacent spermatogenic cells. In the present study we have analyzed the production of PAs by retinoid-treated rat Sertoli cells. In addition, because retinoids modulate the response of Sertoli cells to FSH either potentiating or antagonizing its action, we have investigated a possible modulation of FSH-stimulated PA production. Under basal conditions, Sertoli cells, isolated from prepubertal rats, secrete predominantly uPA. A significant dose-dependent inhibition of uPA activity was observed after treatment with retinol, while no significant effect was detected upon tPA secretion. When Sertoli cells were cultured in the presence of 0.25 microM retinol, a significant inhibition of uPA activity was evident after 16 h of treatment and reached approximately 80% after 48 h of treatment. The analysis of the mRNA levels revealed that retinol induces an inhibition of the steady-state levels of uPA mRNA without affecting those of tPA. Moreover, retinol affected uPA mRNA levels by increasing mRNA turnover. The effect of retinoids on Sertoli cells isolated from older animals was less evident, possibly due to the reduced production of uPA with the increase of age of the donor animals. Our results on the effect of retinoids upon Sertoli cell uPA production reinforce the importance of retinoids in the control of postnatal testis development.
组织型(t)和尿激酶型(u)纤溶酶原激活剂(PA)已被证明由生精小管中的支持细胞以周期性方式分泌,并依赖于促卵泡激素(FSH)刺激或相邻生精细胞的存在。在本研究中,我们分析了经视黄酸处理的大鼠支持细胞中PA的产生。此外,由于视黄酸可调节支持细胞对FSH的反应,增强或拮抗其作用,我们研究了视黄酸对FSH刺激的PA产生的可能调节作用。在基础条件下,从青春期前大鼠分离的支持细胞主要分泌uPA。用视黄醇处理后,观察到uPA活性有显著的剂量依赖性抑制,而tPA分泌未检测到显著影响。当支持细胞在0.25 microM视黄醇存在下培养时,处理16小时后uPA活性明显受到显著抑制,处理48小时后达到约80%。mRNA水平分析显示,视黄醇诱导uPA mRNA稳态水平的抑制,而不影响tPA的稳态水平。此外,视黄醇通过增加mRNA周转来影响uPA mRNA水平。视黄酸对从年龄较大动物分离的支持细胞的作用不太明显,这可能是由于供体动物年龄增加导致uPA产生减少。我们对视黄酸对支持细胞uPA产生影响的结果强化了视黄酸在出生后睾丸发育控制中的重要性。