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大鼠垂体中生长抑素-28的超微结构放射自显影定位

Ultrastructural autoradiographic localization of somatostatin-28 in the rat pituitary gland.

作者信息

Morel G, Leroux P, Pelletier G

出版信息

Endocrinology. 1985 Apr;116(4):1615-20. doi: 10.1210/endo-116-4-1615.

Abstract

To identify the anterior pituitary cell type(s) containing somatostatin-28 (SS-28)-binding sites and to study the internalization processes of this peptide by the target cells, autoradiography was performed on rat anterior pituitaries removed at specific intervals (2-60 min) after iv injection of the [125I]iodo-SS-28 agonist [Leu8,D-Trp22,Tyr25]SS-28 into intact, adrenalectomized, or castrated male rats. At the light microscopic level, the silver grains were found in 75% of cells. Concomitant injection of an excess of unlabeled peptide prevented the binding of label, verifying the specificity of binding. No specific labeling could be detected in the adrenocorticotrophs of adrenalectomized rats or gonadotrophs (castration cells) of castrated rats. At the electron microscopic level, three cell types (somatotrophs, thyrotrophs, and mammotrophs) appear to contain radiolabeled SS-28. The time-course study in somatotrophs of intact animals showed that 2 min after injection, most silver grains were associated with the plasma membrane. Five to 15 min after injection, label was found over both the plasma membrane and cytoplasmic organelles, especially the Golgi apparatus, lysosomes, and secretory granules. At the longest time interval (60 min), labeling was mostly associated with the cytoplasmic organelles. These results indicate that SS-28-binding sites are present only in those cell types in which somatostatin is known to regulate secretory functions. The present data also show that a rapid internalization of the radiolabeled peptide occurs.

摘要

为了鉴定含有生长抑素 - 28(SS - 28)结合位点的垂体前叶细胞类型,并研究该肽被靶细胞内化的过程,在向完整、肾上腺切除或阉割的雄性大鼠静脉注射[125I]碘 - SS - 28激动剂[Leu8,D - Trp22,Tyr25]SS - 28后,于特定时间间隔(2 - 60分钟)取出大鼠垂体前叶进行放射自显影。在光学显微镜水平,75%的细胞中发现了银颗粒。同时注射过量未标记的肽可阻止标记物的结合,证实了结合的特异性。在肾上腺切除大鼠的促肾上腺皮质激素细胞或阉割大鼠的促性腺激素细胞(阉割细胞)中未检测到特异性标记。在电子显微镜水平,三种细胞类型(生长激素细胞、促甲状腺激素细胞和催乳激素细胞)似乎含有放射性标记的SS - 28。对完整动物生长激素细胞的时间进程研究表明,注射后2分钟,大多数银颗粒与质膜相关。注射后5至15分钟,质膜和细胞质细胞器,尤其是高尔基体、溶酶体和分泌颗粒上均发现标记物。在最长时间间隔(60分钟)时,标记物大多与细胞质细胞器相关。这些结果表明,SS - 28结合位点仅存在于已知生长抑素调节分泌功能的细胞类型中。目前的数据还表明,放射性标记的肽会迅速内化。

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