Martin J E, Klein D C
Endocrinology. 1976 Nov;99(5):1189-98. doi: 10.1210/endo-99-5-1189.
An organ culture system for neonatal rat anterior pituitary glands has been developed in which cellular integrity and responsiveness to LH releasing hormone (LHRH) are maintained for at least 4 days. Anterior pituitary glands from Sprague-Dawley rats were cultured individually at 37 C in an atmosphere of 95% O2-5% CO2 in BGJb culture medium, Fitton-Jackson modification. Histological examination of 5-day-old rat pituitary glands cultured for 96 h in control medium revealed no evidence of tissue necrosis. By contrast, 40-day-old-rat anterior pituitary glands were centrally necrotic after only 24 h of incubation under the same conditions. The neonatal glands were treated for 24 h with synthetic LHRH, and medium and pituitary LH FSH concentrations were determined by double antibody radioimmunoassay. On the first day of culture, LHRH caused a dose-related release of LH with the minimal effective dose between 10(-10) and 10(-9)M. Near-maximal release appeared to be attained with 10(-6)M LHRH, which induced a 12-fold elevation in medium LH over controls. Release was evident within 3 h following stimulation with 10(-9)M LHRH. Pituitary glands were responsive to this dose at 0,24 and 72 h of culture with progressively increasing ratios between LHRH-stimulated and control LH levels of 3,13, and 24, respectively. Although FSH release by LHRH was not observed on the first day of culture, on the second day LHRH caused a dose-related secretion of this hormone. Specificity of the pituitary response was demonstrated for LH and TSH release following addition of LHRH and thyrotropin releasing hormone (TRH). The simplicity, sensitivity, reproducibility, and long-term viability of this neonatal rat anterior pituitary organ culture system make it a valuable technique for the study of gonadotropin secretion.
已开发出一种新生大鼠垂体前叶器官培养系统,在该系统中细胞完整性和对促黄体生成素释放激素(LHRH)的反应性可维持至少4天。将来自斯普拉格-道利大鼠的垂体前叶在37℃、95% O₂ - 5% CO₂ 气氛下,于改良的BGJb培养基(Fitton-Jackson改良型)中单独培养。对在对照培养基中培养96小时的5日龄大鼠垂体进行组织学检查,未发现组织坏死迹象。相比之下,40日龄大鼠的垂体前叶在相同条件下仅孵育24小时后就出现中央坏死。用合成LHRH处理新生腺体24小时,然后通过双抗体放射免疫测定法测定培养基和垂体中LH、FSH的浓度。在培养的第一天,LHRH引起LH呈剂量相关的释放,最小有效剂量在10⁻¹⁰至10⁻⁹M之间。10⁻⁶M LHRH似乎能达到接近最大的释放量,它使培养基中LH水平比对照升高了12倍。用10⁻⁹M LHRH刺激后3小时内释放明显。垂体在培养0、24和72小时时对该剂量有反应,LHRH刺激的LH水平与对照LH水平之比分别逐渐增加至3、13和24。虽然在培养第一天未观察到LHRH诱导FSH释放,但在第二天LHRH引起了该激素的剂量相关分泌。添加LHRH和促甲状腺激素释放激素(TRH)后,垂体对LH和TSH释放的反应具有特异性。这种新生大鼠垂体前叶器官培养系统的简单性、敏感性、可重复性和长期生存能力使其成为研究促性腺激素分泌的一项有价值的技术。