Hiney J K, Sower S A, Yu W H, McCann S M, Dees W L
Department of Veterinary Anatomy and Public Health, College of Veterinary Medicine, Texas A&M University, College Station, TX 77843-4458, USA.
Proc Natl Acad Sci U S A. 2002 Feb 19;99(4):2386-91. doi: 10.1073/pnas.042699799. Epub 2002 Feb 12.
This study utilized a newly developed antiserum, specific for lamprey gonadotropin-releasing hormone III (l-GnRH-III), to determine the following: in which regions of the rat hypothalamus the neuronal perikarya producing l-GnRH-III are localized; and whether this peptide, known to selectively induce follicle-stimulating hormone release, is coexpressed in neurons containing mammalian luteinizing hormone-releasing hormone (m-LHRH). Double-label immunocytochemistry was performed by using an l-GnRH-III polyclonal antiserum and an LHRH monoclonal antiserum. Immunopositive neurons for l-GnRH-III, m-LHRH, or neurons coexpressing both peptides were detected within the organum vasculosum lamina terminalis (OVLT) region of the preoptic area (POA). Caudal to the OVLT, l-GnRH-III-positive neurons were also observed dorso-medially, above the third ventricle in the medial POA. The m-LHRH neurons were not observed in this area. The lateral POA region contained neurons positive for both peptides along with single-labeled neurons for each peptide. Importantly, neurons that expressed l-GnRH-III, m-LHRH, or both peptides were also detected in the ventral regions of the rostral hypothalamus, dorsolateral to the borders of the supraoptic nuclei. In both of these latter areas, neurons containing l-GnRH-III were slightly dorsal to neurons containing only m-LHRH. The l-GnRH-III perikarya and fibers were eliminated by absorption of the primary antiserum with l-GnRH-III, but not by l-GnRH-I, chicken-GnRH-II, or m-LHRH. These results indicate that, unlike other isoforms of GnRH found in the mammalian brain, l-GnRH-III neurons not only are observed in regions that control follicle-stimulating hormone release but also are colocalized with m-LHRH neurons in areas primarily controlling LH release. These findings suggest an interrelationship between these two peptides in the control of gonadotropin secretion.
本研究利用一种新开发的、对七鳃鳗促性腺激素释放激素III(l-GnRH-III)具有特异性的抗血清来确定以下内容:产生l-GnRH-III的神经元胞体在大鼠下丘脑的哪些区域定位;以及这种已知能选择性诱导促卵泡激素释放的肽是否在含有哺乳动物促黄体生成素释放激素(m-LHRH)的神经元中共同表达。通过使用l-GnRH-III多克隆抗血清和LHRH单克隆抗血清进行双重标记免疫细胞化学。在视前区(POA)的终板血管器(OVLT)区域内检测到了l-GnRH-III、m-LHRH的免疫阳性神经元或同时表达这两种肽的神经元。在OVLT的尾侧,在内侧POA第三脑室上方的背内侧也观察到了l-GnRH-III阳性神经元。在该区域未观察到m-LHRH神经元。外侧POA区域包含两种肽均呈阳性的神经元以及每种肽的单标记神经元。重要的是,在 Rostral 下丘脑的腹侧区域,视上核边界的背外侧也检测到了表达l-GnRH-III、m-LHRH或两种肽的神经元。在这两个后一个区域中,含有l-GnRH-III的神经元都略位于仅含有m-LHRH的神经元的背侧。l-GnRH-III的胞体和纤维通过用l-GnRH-III吸收一抗而被消除,但用l-GnRH-I、鸡GnRH-II或m-LHRH则不会。这些结果表明,与在哺乳动物大脑中发现的其他GnRH同工型不同,l-GnRH-III神经元不仅在控制促卵泡激素释放的区域中被观察到,而且在主要控制促黄体生成素释放的区域中与m-LHRH神经元共定位。这些发现提示了这两种肽在促性腺激素分泌控制中的相互关系。