Jamaluddin M, Banerjee P P, Manna P R, Bhattacharya S
Department of Zoology, School of Life Sciences, Visva-Bharati University, Santiniketan, West Bengal, India.
Gen Comp Endocrinol. 1989 May;74(2):190-8. doi: 10.1016/0016-6480(89)90212-8.
Influence of extracellular calcium on gonadotropin hormone-releasing hormone (GnRH)-stimulated gonadotropin hormone (GtH) release from a teleostean fish (Channa punctatus) pituitary was examined in vitro by preparing enzymatically dispersed pituitary cell incubation. Effect of Ca2+ on GnRH-augmented GtH release was evaluated with partially purified C. punctatus GnRH (cGnRH) and synthetic mammalian GnRH (mGnRH). Cells were dispersed by 0.3% collagenase plus 0.05% trypsin in culture medium and a high yield of viable cells were obtained. Addition of cGnRH (10 micrograms/ml) to pituitary cells in Ca2+-free medium resulted in a significant increase in GtH release, but the addition of Ca2+ (2 mM) enhanced it to about four- and threefold over cGnRH and mGnRH, respectively. Increasing concentrations of Ca2+ (0.1-2.0 mM/well) with fixed concentrations of GnRH (10 micrograms/ml) or increasing doses of GnRH (2.5 to 20 micrograms/ml) with fixed amount of Ca2+ (2 mM/well) resulted in a dose dependent increase in GtH release. EDTA or EGTA (2 mM/well) completely suppressed the Ca2+-augmenting effect of GnRH-stimulated GtH release. Addition of lanthanum (La3+, 4 mM/well), a competitive inhibitor of Ca2+, reduced 60% of the Ca2+ (2 mM/well) stimulation. Verapamil, a specific Ca2+ channel blocker, when added in increasing concentrations (1-100 microM/well) to pituitary cell incubations containing GnRH-stimulated GtH release in Ca2+-free medium could be waived by EGTA (2 mM/well), indicating availability of extracellular calcium from tissue sources. The uptake of radioactive Ca2+ by pituitary cells was greatly enhanced by GnRH while the addition of verapamil (10 microM/well) not only inhibited the GnRH-stimulated uptake, but also reduced it below the control level.(ABSTRACT TRUNCATED AT 250 WORDS)
通过制备酶解分散的垂体细胞培养物,在体外研究了细胞外钙对硬骨鱼类(斑鳢)垂体中促性腺激素释放激素(GnRH)刺激的促性腺激素(GtH)释放的影响。用部分纯化的斑鳢GnRH(cGnRH)和合成的哺乳动物GnRH(mGnRH)评估了Ca2+对GnRH增强的GtH释放的作用。细胞在培养基中用0.3%胶原酶加0.05%胰蛋白酶进行分散,获得了高产量的活细胞。在无Ca2+培养基中向垂体细胞添加cGnRH(10微克/毫升)导致GtH释放显著增加,但添加Ca2+(2毫摩尔/升)分别使其比cGnRH和mGnRH增强约四倍和三倍。在固定浓度的GnRH(10微克/毫升)下增加Ca2+浓度(0.1 - 2.0毫摩尔/孔)或在固定量的Ca2+(2毫摩尔/孔)下增加GnRH剂量(2.5至20微克/毫升)导致GtH释放呈剂量依赖性增加。EDTA或EGTA(2毫摩尔/孔)完全抑制了GnRH刺激的GtH释放的Ca2+增强作用。添加镧(La3+,4毫摩尔/孔),一种Ca2+的竞争性抑制剂,减少了60%的Ca2+(2毫摩尔/孔)刺激。维拉帕米,一种特异性Ca2+通道阻滞剂,当以增加的浓度(1 - 100微摩尔/孔)添加到在无Ca2+培养基中含有GnRH刺激的GtH释放的垂体细胞培养物中时,可被EGTA(2毫摩尔/孔)消除,表明可从组织来源获得细胞外钙。GnRH极大地增强了垂体细胞对放射性Ca2+的摄取,而添加维拉帕米(10微摩尔/孔)不仅抑制了GnRH刺激的摄取,还将其降低到对照水平以下。(摘要截断于250字)