Fukata J, Diamond D J, Martin J B
Endocrinology. 1985 Aug;117(2):457-67. doi: 10.1210/endo-117-2-457.
The effects of rat hypothalamic GH-releasing factor (GRF) and somatostatin (SRIF) on the release and biosynthesis of rat GH were studied by RIA and quantitative immunoprecipitation using monolayer cultures of rat anterior pituitary cells. In kinetic studies, GRF stimulation of GH release appeared at the first sampling time (20-min incubation) and the effect began to diminish after 2-h incubation with GRF. On the other hand, total (cell plus medium) content of GH significantly increased only after 24-h incubation. To examine the GH-synthesizing effect of GRF more directly, newly synthesized GH labeled by [35S]methionine during incubation with GRF was quantified by immunoprecipitation. The amount of immunoprecipitable GH increased significantly and specifically (compared with the total amount of labeled proteins) also only after 24-h incubation. When GH pools were labeled with [35S]methionine under different schedules, the basal release of newly synthesized GH, which was labeled for 1 h immediately before chase incubation was lower during the first 15 min than stored GH which had been labeled earlier. Basal newly synthesized GH secretion exceeded stored GH secretion after 30 min. GRF stimulated the release of GH from both pools but the stimulation of stored GH was greater. In this system, SRIF suppressed both the basal and stimulated release of GH but did not modify GH biosynthesis under either condition. Newly synthesized GH showed significant degradation during 24-h incubation; neither GRF nor SRIF affected the rate of GH degradation during the same incubation period. These results indicate that 1) GRF stimulates both release and synthesis of GH; 2) these two effects have different kinetics and different sensitivities to SRIF; and 3) GRF stimulates the release of GH from heterogeneous pools disproportionally.
采用放射免疫分析法(RIA)和定量免疫沉淀法,利用大鼠垂体前叶细胞单层培养物,研究了大鼠下丘脑生长激素释放因子(GRF)和生长抑素(SRIF)对大鼠生长激素(GH)释放和生物合成的影响。在动力学研究中,GRF对GH释放的刺激作用在首次取样时间(孵育20分钟)时就已出现,且在与GRF孵育2小时后,这种作用开始减弱。另一方面,只有在孵育24小时后,GH的总含量(细胞内加培养基中的)才显著增加。为了更直接地检测GRF对GH合成的作用,通过免疫沉淀法定量分析了在与GRF孵育期间用[35S]甲硫氨酸标记的新合成的GH。同样,只有在孵育24小时后,可免疫沉淀的GH量才显著且特异性地增加(与标记蛋白的总量相比)。当在不同的时间安排下用[35S]甲硫氨酸标记GH库时,在追踪孵育前立即标记1小时的新合成GH的基础释放量,在最初15分钟内低于较早标记的储存GH。30分钟后,新合成GH的基础分泌量超过了储存GH的分泌量。GRF刺激了这两个GH库中GH的释放,但对储存GH的刺激作用更大。在这个系统中,SRIF抑制了GH的基础释放和刺激释放,但在两种情况下均未改变GH的生物合成。在24小时的孵育过程中,新合成的GH出现了显著降解;在相同的孵育期内,GRF和SRIF均未影响GH的降解速率。这些结果表明:1)GRF刺激GH的释放和合成;2)这两种作用具有不同的动力学以及对SRIF的不同敏感性;3)GRF对不同GH库中GH释放的刺激作用不均衡。