Silverman A J, Witkin J W, Millar R P
Department of Anatomy and Cell Biology, College of Physicians and Surgeons, Columbia University, New York, New York 10032.
J Histochem Cytochem. 1990 Jun;38(6):803-13. doi: 10.1177/38.6.2186087.
A battery of antibodies directed against different portions of the precursor to gonadotropin-releasing hormone (GnRH), as well as to the mature decapeptide, were characterized immunocytochemically in two ways. Absorption experiments were used to determine the epitope recognized by each antiserum. Electron microscopic immunocytochemistry was then used to define the subcellular organelles that contained reaction product when tissue was incubated with these reagents. These latter observations helped to determine if the antibody recognized the epitope as part of the intact precursor or only after it had been cleaved from parent protein. Our results demonstrate that the GnRH precursor is routed from the rough endoplasmic reticulum through the Golgi apparatus to the secretory vesicles. Furthermore, we show that initial cleavage and processing of the GnRH precursor begin in the cell soma. These antibodies should be useful in the future in determining changes in processing of precursor in animals that differ in endocrine function.
一组针对促性腺激素释放激素(GnRH)前体不同部分以及成熟十肽的抗体,通过两种方式进行了免疫细胞化学表征。吸收实验用于确定每种抗血清识别的表位。然后,当组织与这些试剂孵育时,利用电子显微镜免疫细胞化学来确定含有反应产物的亚细胞器。这些后续观察有助于确定抗体识别的表位是完整前体的一部分,还是仅在其从母体蛋白裂解后才识别。我们的结果表明,GnRH前体从粗面内质网经高尔基体转运至分泌小泡。此外,我们还表明,GnRH前体的初始裂解和加工始于细胞体。这些抗体未来应有助于确定内分泌功能不同的动物中前体加工过程的变化。