Vogel D L, Magner J A, Sherins R J, Weintraub B D
Endocrinology. 1986 Jul;119(1):202-13. doi: 10.1210/endo-119-1-202.
We have studied the de novo biosynthesis and secretion of LH subunits in pituitary quarters from orchiectomized and intact control adult male rats and their regulation by GnRH. After labeling with [35S]cystine ([35S]Cys), [35S]methionine, or [3H]glucosamine ([3H]GlcN) in the presence or absence of 10(-8) M GnRH, tissue lysates and media were immunoprecipitated with antisera to LH beta, then LH alpha (after removal of TSH by immunoprecipitation with anti-TSH beta), and the products were analyzed by sodium dodecyl sulfate gradient gel electrophoresis. During a 12-min pulse labeling with [35S]methionine, three forms of immunoreactive alpha were labeled at 21,000, 18,000, and 12,000 mol wt. After a 30-min chase with excess unlabeled methionine, the 12,000 form decreased from 10% to 3% of total radioactivity, while the 21,000 form increased from 57% to 69%, implying a precursor-product relationship. Neither orchiectomy nor GnRH had any effect on [35S]Cys or [3H]GlcN incorporation into intracellular or secreted total proteins. After a 6-h continuous labeling, incorporation of [35S]Cys into intracellular combined LH alpha in castrates was 158% of the control value, combined LH beta was 304%, and free alpha was 466%. The [3H]GlcN to [35S]Cys ratio, reflecting relative glycosylation, was unchanged in castrates for total proteins or LH alpha and somewhat decreased for LH beta and free alpha. Orchiectomy increased [35S]Cys-labeled secreted LH beta and free alpha to 183% and 231% of control values, respectively. Relative glycosylation of secreted LH alpha, LH beta, and free alpha was unchanged in castrates. Incorporation of [35S]Cys into intracellular combined LH alpha, LH beta and free alpha-subunit was unaffected by GnRH in pituitaries from intact rats. In castrates, LH alpha was unchanged, but LH beta and free alpha were slightly increased. Incorporation of [3H]GlcN into intracellular combined LH alpha, LH beta, and free alpha was increased with GnRH in both intacts and castrates, such that the 3H to 35S ratio, reflecting relative glycosylation, was also increased with GnRH. In castrates, the ratios, as a percentage of the control, were, respectively 250%, 250%, and 223% for LH alpha, LH beta, and free alpha. In intact animals, the ratios were 221%, 281%, and 143%, respectively. Incorporation of both [35S]Cys and [3H]GlcN into secreted subunits was increased in most instances, such that the 3H to 35S ratio was increased only for LH beta.(ABSTRACT TRUNCATED AT 400 WORDS)
我们研究了去势成年雄性大鼠和完整对照成年雄性大鼠垂体各部分中促黄体生成素(LH)亚基的从头生物合成和分泌,以及促性腺激素释放激素(GnRH)对其的调节作用。在用[35S]胱氨酸([35S]Cys)、[35S]甲硫氨酸或[3H]葡糖胺([3H]GlcN)进行标记时,无论有无10(-8)M GnRH,组织裂解物和培养基先用抗LHβ抗血清进行免疫沉淀,然后用抗TSHβ抗血清免疫沉淀去除促甲状腺激素(TSH)后,再用抗LHα抗血清进行免疫沉淀,产物通过十二烷基硫酸钠梯度凝胶电泳进行分析。在用[35S]甲硫氨酸进行12分钟脉冲标记期间,三种形式的免疫反应性α被标记,分子量分别为21,000、18,000和12,000道尔顿。在用过量未标记甲硫氨酸进行30分钟追踪后,12,000道尔顿的形式占总放射性的比例从10%降至3%,而21,000道尔顿的形式从57%增至69%,这意味着存在前体-产物关系。去势和GnRH对[35S]Cys或[3H]GlcN掺入细胞内或分泌的总蛋白均无影响。在进行6小时连续标记后,去势大鼠细胞内结合的LHα中[35S]Cys的掺入量是对照值的158%,结合的LHβ是304%,游离α是466%。反映相对糖基化的[3H]GlcN与[35S]Cys的比率,对于总蛋白、LHα在去势大鼠中未改变,对于LHβ和游离α略有下降。去势使[35S]Cys标记分泌的LHβ和游离α分别增加至对照值的183%和231%。去势大鼠中分泌的LHα、LHβ和游离α的相对糖基化未改变。在完整大鼠的垂体中,GnRH对[35S]Cys掺入细胞内结合的LHα、LHβ和游离α亚基无影响。在去势大鼠中,LHα未改变,但LHβ和游离α略有增加。在完整大鼠和去势大鼠中,GnRH均使[3H]GlcN掺入细胞内结合的LHα、LHβ和游离α增加,因此反映相对糖基化的3H与35S的比率也随GnRH增加。在去势大鼠中,LHα、LHβ和游离α的比率相对于对照的百分比分别为250%、250%和223%。在完整动物中,比率分别为221%、281%和143%。在大多数情况下,[35S]Cys和[3H]GlcN掺入分泌亚基均增加,因此仅LHβ的3H与35S比率增加。(摘要截短至400字)