Reubi J C, Laissue J A, Waser B, Steffen D L, Hipkin R W, Schonbrunn A
Division of Cell Biology and Experimental Cancer Research, Institute of Pathology, University of Berne, Switzerland.
J Clin Endocrinol Metab. 1999 Aug;84(8):2942-50. doi: 10.1210/jcem.84.8.5878.
The cellular distribution of the somatostatin sst2A receptor protein was investigated in the lymphatic, smooth muscular, and nervous components of the human gastrointestinal tract using subtype-specific antibody R2-88 for immunohistochemical staining of cryostat and formalin-fixed, paraffin-embedded tissue sections. Germinal centers of intestinal lymphatic follicles were immunostained, exhibiting a predominantly plasma membrane localization of the receptor. Similarly, nerve fibers and cells in the submucosal and myenteric plexus were stained for sst2A. Antibody preabsorption with 100 nmol/L antigen peptide abolished staining in all of these tissues, and immunohistochemical staining correlated with the labeling observed after receptor autoradiography using the sst2-preferring radioligand 125I-[Tyr3]octreotide. Cytoplasmic immunostaining was detected in gastrointestinal smooth muscle cells and was inhibited by antibody pre-absorption with antigen peptide. However, 125I-[Tyr3]octreotide autoradiography was negative, and Western blots showed no band at the usual 70-90 kDa location for sst2A. Instead, a band was observed at 205 kDa. This band comigrated with the rabbit myosin standard, which was also stained with R2-88, although antibody sensitivity for myosin was less than 0.002% of that for the sst2A receptor. Rigorous computer-based sequence analysis demonstrated the peptide sequence chosen for antibody production was unique. Moreover, standard sequence alignment protocols were unable to identify the sequences in myosin responsible for the observed reactivity with the R2-88 antiserum. The observed cross-reactivity emphasizes the need for extensive controls to prove the specificity of immunostaining for such low abundance proteins as receptors even when the peptide sequence chosen for antibody production is unique. This study demonstrates for the first time the presence of specific sst2A receptor protein by immunohistochemistry in the human gastrointestinal lymphatic and nervous components, but not in gastrointestinal circular and longitudinal smooth muscle.
利用亚型特异性抗体R2 - 88对恒冷箱切片以及福尔马林固定、石蜡包埋的组织切片进行免疫组织化学染色,研究生长抑素sst2A受体蛋白在人胃肠道的淋巴、平滑肌和神经成分中的细胞分布。肠道淋巴滤泡的生发中心呈免疫染色,显示该受体主要定位于质膜。同样,黏膜下和肌间神经丛中的神经纤维和细胞也被sst2A染色。用100 nmol/L抗原肽进行抗体预吸附可消除所有这些组织中的染色,并且免疫组织化学染色与使用sst2偏好性放射性配体125I - [Tyr3]奥曲肽进行受体放射自显影后观察到的标记相关。在胃肠道平滑肌细胞中检测到细胞质免疫染色,并且用抗原肽进行抗体预吸附可抑制该染色。然而,125I - [Tyr3]奥曲肽放射自显影呈阴性,并且蛋白质印迹法在通常sst2A的70 - 90 kDa位置未显示条带。相反,在205 kDa处观察到一条带。这条带与兔肌球蛋白标准品迁移一致,兔肌球蛋白标准品也被R2 - 88染色,尽管抗体对肌球蛋白的敏感性小于对sst2A受体敏感性的0.002%。基于计算机的严格序列分析表明,用于产生抗体的肽序列是独特的。此外,标准序列比对方案无法识别肌球蛋白中与观察到的与R2 - 88抗血清反应性相关的序列。观察到的交叉反应强调了对于证明针对受体等低丰度蛋白的免疫染色特异性需要进行广泛对照,即使所选择的用于产生抗体的肽序列是独特的。本研究首次通过免疫组织化学证明在人胃肠道的淋巴和神经成分中存在特异性sst2A受体蛋白,但在胃肠道环行和纵行平滑肌中不存在。