Verhoeven G, Cailleau J
Mol Cell Endocrinol. 1985 Apr;40(1):57-68. doi: 10.1016/0303-7207(85)90158-3.
We investigated whether Sertoli cell spent media (SCM) contain a factor (or factors) which influences steroidogenesis in Leydig cells. Freshly prepared prepubertal interstitial cells or Percoll-purified Leydig cells and similar cells cultured in the presence or absence of LH were incubated for 24 h in the presence of a 5 alpha-reductase inhibitor and in the presence or absence of SCM. The accumulation of C19-steroids (testosterone and androstenedione), C21-steroids (progesterone, 17 alpha-hydroxyprogesterone and 20 alpha-hydroxypregn-4-en-3-one) and cyclic AMP was measured by radioimmunoassay. It could be demonstrated that SCM contains a factor that stimulates an early step in the steroidogenic pathway but at the same time hampers the conversion of C21-precursors into androgens. In freshly prepared Leydig cells the final effect is a stimulation of the androgen output. In Leydig cells cultured in the absence of LH, mainly C21-steroid output is increased. These biological effects resemble those observed with LHRH and its agonists. The activity of the Sertoli cell factor is not affected by an LHRH antagonist, however, and maximally effective concentrations of the factor and LHRH have additive effects, suggesting that they act by distinct receptor systems. Preliminary characterization shows that the factor in SCM is a thermolabile protein with a MW greater than 10 000. The production of the factor decreases during prolonged culture in serum-free medium. Addition of fetal calf serum causes a marked and dose-dependent increase in the production or activity of the factor. Several permanent cell lines (B16, Bowes, BHK, Ratec, RK13, Vero) produce a factor with comparable biological effects on Leydig cells. Nonetheless, the observation that the production of this factor by Sertoli cell cultures is stimulated by FSH and dbcAMP suggests that, in the testis, it may play a role in the paracrine control of Leydig cell function.
我们研究了支持细胞条件培养基(SCM)是否含有影响睾丸间质细胞类固醇生成的一种或多种因子。将新制备的青春期前间质细胞或经Percoll纯化的睾丸间质细胞以及在有或无促黄体生成素(LH)情况下培养的类似细胞,在5α-还原酶抑制剂存在下,以及在有或无SCM的情况下孵育24小时。通过放射免疫测定法测量C19类固醇(睾酮和雄烯二酮)、C21类固醇(孕酮、17α-羟孕酮和20α-羟基孕-4-烯-3-酮)和环磷酸腺苷(cAMP)的积累。可以证明,SCM含有一种因子,该因子刺激类固醇生成途径的早期步骤,但同时阻碍C21前体向雄激素的转化。在新制备的睾丸间质细胞中,最终效果是刺激雄激素的产生。在无LH培养的睾丸间质细胞中,主要是C21类固醇的产生增加。这些生物学效应类似于促性腺激素释放激素(LHRH)及其激动剂所观察到的效应。然而,支持细胞因子的活性不受LHRH拮抗剂的影响,并且该因子和LHRH的最大有效浓度具有相加效应,表明它们通过不同的受体系统起作用。初步表征表明,SCM中的因子是一种热不稳定蛋白,分子量大于10000。在无血清培养基中长时间培养期间,该因子的产生会减少。添加胎牛血清会导致该因子的产生或活性显著且呈剂量依赖性增加。几种永久细胞系(B16、Bowes、BHK、Ratec、RK13、Vero)产生对睾丸间质细胞具有类似生物学效应的因子。尽管如此,支持细胞培养物产生该因子受到促卵泡激素(FSH)和二丁酰环磷腺苷(dbcAMP)刺激这一观察结果表明,在睾丸中,它可能在旁分泌调节睾丸间质细胞功能中发挥作用。