Ailenberg M, McCabe D, Fritz I B
Banting and Best Department of Medical Research, University of Toronto, Ontario, Canada.
Endocrinology. 1990 Mar;126(3):1561-8. doi: 10.1210/endo-126-3-1561.
The addition of androgens (testosterone or dihydrotestosterone) resulted in decreased levels of detectable plasminogen activator activity in the medium when Sertoli cells were maintained in culture in a serum-free chemically defined medium in a two-chambered assembly. This occurred in the presence or absence of extracellular matrix or peritubular cells in the system. In the complete two-chambered assembly, addition of androgens simultaneously resulted in a small but significant increase in the integrity of the Sertoli cell barrier separating the two chambers, as indicated by slower rates of equilibration of [3H]methoxyinulin between inner and outer chambers. These responses to steroids appeared to be androgen specific, since other steroids examined (17 beta-estradiol, progesterone, and dexamethasone) had no detectable effects on levels of plasminogen activator activities or on barrier function. We confirmed that when FSH or (Bu)2cAMP is added to stimulate plasminogen activator secretion by Sertoli cells, the integrity of the barrier is decreased, provided no antiproteases are present in the serum-free medium. Simultaneous addition of androgens inhibited these effects of (Bu)2cAMP on Sertoli cells, but did not influence the responses of Sertoli cells to FSH. We compare actions of androgens on Sertoli cells in culture under various conditions and discuss the possible physiological significance of the inhibition of plasminogen activator activity.
当支持细胞在两室装置中于无血清化学限定培养基中培养时,添加雄激素(睾酮或双氢睾酮)会导致培养基中可检测到的纤溶酶原激活物活性水平降低。无论系统中是否存在细胞外基质或睾丸间质细胞,都会出现这种情况。在完整的两室装置中,添加雄激素同时会使分隔两室的支持细胞屏障完整性有小幅但显著的增加,这可通过[3H]甲氧基菊粉在内外室之间的平衡速率减慢来表明。对类固醇的这些反应似乎具有雄激素特异性,因为所检测的其他类固醇(17β - 雌二醇、孕酮和地塞米松)对纤溶酶原激活物活性水平或屏障功能均无可检测到的影响。我们证实,当添加促卵泡激素(FSH)或双丁酰环磷腺苷((Bu)2cAMP)以刺激支持细胞分泌纤溶酶原激活物时,若无血清培养基中不存在抗蛋白酶,则屏障的完整性会降低。同时添加雄激素可抑制(Bu)2cAMP对支持细胞的这些作用,但不影响支持细胞对FSH的反应。我们比较了雄激素在各种条件下对培养的支持细胞的作用,并讨论了抑制纤溶酶原激活物活性的可能生理意义。