May V, Eipper B A
Endocrinology. 1986 Apr;118(4):1284-95. doi: 10.1210/endo-118-4-1284.
Insulin, transferrin, and serum albumin were found to be essential additives for maintenance of primary rat pituitary ACTH/endorphin cells in complete serum-free defined medium (CSFM). Primary anterior pituitary cultures maintained in CSFM exhibited a 3- to 5-fold increase in cell content of ACTH/endorphin-related peptide during the first 2 weeks in culture, and this level remained stable for at least the next week. Immunocytochemical and morphometric studies indicated that the number of corticotropes increased only slightly, so that hormone content per corticotrope increased. Anterior pituitary cultures maintained in CSFM exhibited a basal secretory rate of 0.3-0.4% of cell hormone content/h throughout the 3-week period in culture, and total hormone production increased 6-fold. Primary anterior pituitary cultures maintained chronically in CSFM containing 10 nM CRF demonstrated a 15- to 20-fold increase in total ACTH/endorphin production over 3 weeks in culture. Chronic treatment with CRF brought about a sustained 6-fold increase in secretory rate (2.5% of cell hormone content/h), and corticotrope content of hormone was diminished 3-fold. Corticotropes maintained chronically in CSFM containing CRF did not increase in number and exhibited a rim of immunocytochemically identifiable hormone around the cell periphery. Anterior pituitary cultures maintained chronically in CSFM containing 100 nM dexamethasone (DEX) exhibited decreased cell hormone content and an unaltered secretory rate. In the DEX-treated cultures the number of immunocytochemically identifiable corticotropes declined, as did the staining intensity per corticotrope. Primary cultures of rat intermediate pituitary cells maintained in CSFM exhibited a 1.5- to 2-fold increase in hormone content after 1-2 weeks in culture, maintained a constant basal secretory rate of 0.4-0.5% cell content/h, and were not responsive to chronic treatment with CRF or DEX.
胰岛素、转铁蛋白和血清白蛋白被发现是在完全无血清限定培养基(CSFM)中维持原代大鼠垂体促肾上腺皮质激素/内啡肽细胞所必需的添加剂。在CSFM中维持的原代垂体前叶培养物在培养的前2周内促肾上腺皮质激素/内啡肽相关肽的细胞含量增加了3至5倍,并且该水平在至少接下来的一周内保持稳定。免疫细胞化学和形态计量学研究表明促肾上腺皮质激素细胞数量仅略有增加,因此每个促肾上腺皮质激素细胞的激素含量增加。在CSFM中维持的垂体前叶培养物在整个3周的培养期内基础分泌率为细胞激素含量的0.3 - 0.4%/小时,总激素产量增加了6倍。长期在含有10 nM促肾上腺皮质激素释放因子(CRF)的CSFM中维持的原代垂体前叶培养物在3周的培养期内促肾上腺皮质激素/内啡肽总产量增加了15至20倍。用CRF进行慢性处理导致分泌率持续增加6倍(细胞激素含量的2.5%/小时),并且促肾上腺皮质激素细胞的激素含量减少了3倍。长期在含有CRF的CSFM中维持的促肾上腺皮质激素细胞数量没有增加,并且在细胞周边呈现出一圈免疫细胞化学可识别的激素。长期在含有100 nM地塞米松(DEX)的CSFM中维持的垂体前叶培养物细胞激素含量降低,分泌率未改变。在DEX处理的培养物中,免疫细胞化学可识别的促肾上腺皮质激素细胞数量减少,每个促肾上腺皮质激素细胞的染色强度也减少。在CSFM中维持的大鼠垂体中间叶细胞原代培养物在培养1 - 2周后激素含量增加了1.5至2倍,维持0.4 - 0.5%细胞含量/小时的恒定基础分泌率,并且对CRF或DEX的慢性处理无反应。