Schulz S, Schmidt H, Händel M, Schreff M, Höllt V
Department of Pharmacology and Toxicology, Otto-von-Guericke University, Magdeburg, Germany.
Neurosci Lett. 1998 Nov 20;257(1):37-40. doi: 10.1016/s0304-3940(98)00803-9.
We have recently shown that the cytoplasmic tail of the somatostatin receptor sst2 undergoes alternative splicing giving rise to two isoforms, SSt2A and sst2B. In the present study, we have raised polyclonal antibodies that specifically detect either sst2A or sst2B and used these antisera for immunocytochemical localization of the receptor proteins in the rat spinal cord. sst2A-immunoreactivity formed a dense network consisting of neuronal perikarya and dendrites in the superficial layers of the dorsal horn. In contrast, prominent sst2B-immunoreactivity was found on neuronal perikarya and proximal dendrites throughout the gray matter of the spinal cord. Taken together, we show that alternative carboxy-terminal splicing is involved in cell-specific expression of somatostatin receptor sst2 isoforms in rat spinal cord, and that sst2A and sst2B mediate effects of somatostatin at different cellular sites.
我们最近发现,生长抑素受体sst2的胞质尾发生可变剪接,产生了两种异构体,即SSt2A和sst2B。在本研究中,我们制备了特异性检测sst2A或sst2B的多克隆抗体,并使用这些抗血清对大鼠脊髓中的受体蛋白进行免疫细胞化学定位。sst2A免疫反应性在背角浅层形成了一个由神经元胞体和树突组成的密集网络。相比之下,在脊髓灰质的整个区域中,神经元胞体和近端树突上发现了明显的sst2B免疫反应性。综上所述,我们表明羧基末端的可变剪接参与了生长抑素受体sst2异构体在大鼠脊髓中的细胞特异性表达,并且sst2A和sst2B在不同的细胞位点介导生长抑素的作用。