O'Sullivan N L, Montgomery P C
Department of Immunology and Microbiology, Wayne State University School of Medicine, Detroit, Michigan 48201, USA.
Oral Microbiol Immunol. 1996 Oct;11(5):337-42. doi: 10.1111/j.1399-302x.1996.tb00191.x.
Cellular interactions control lymphocyte localization within salivary gland tissues and contribute to the immune defense of oral surfaces. We examined lymphocyte adherence to cultured parotid cells using an in vitro assay and found good correlation with previously reported binding to parotid gland frozen sections. Thoracic duct lymphocytes (TDL) bound to parotid cells in greater numbers than thymocytes (74 vs 11 cells/mm2). B cells showed preferential adherence compared to T cells (75% vs 28%). TDL binding was inhibited by sodium azide or cytochalasin B (60% and 80%, respectively). EDTA inhibition (63%) was restored by replacing calcium (9%) but not magnesium (65%). Binding was inhibited by fucoidin or phosphomannan (approximately 70%). Fibronectin peptides had no effect. Culture supernatants were inhibitory for TDL adherence (60%), suggesting that molecules involved in lymphocyte localization may be shed and that parotid cell cultures will be useful for ligand isolation and characterization.
细胞间相互作用控制淋巴细胞在唾液腺组织中的定位,并有助于口腔表面的免疫防御。我们使用体外试验检测了淋巴细胞与培养的腮腺细胞的黏附情况,发现其与先前报道的淋巴细胞与腮腺腺冷冻切片的结合具有良好的相关性。胸导管淋巴细胞(TDL)与腮腺细胞的结合数量多于胸腺细胞(分别为74个/mm²和11个/mm²)。与T细胞相比,B细胞表现出优先黏附(分别为75%和28%)。叠氮化钠或细胞松弛素B可抑制TDL的结合(分别为60%和80%)。通过补充钙(9%)而非镁(65%)可恢复EDTA抑制作用(63%)。岩藻依聚糖或磷酸甘露聚糖可抑制结合(约70%)。纤连蛋白肽无作用。培养上清液可抑制TDL黏附(60%),这表明参与淋巴细胞定位的分子可能会脱落,并且腮腺细胞培养物将有助于配体的分离和表征。