Timoshenko Alexander V, Gorudko Irina V, Maslakova Olga V, André Sabine, Kuwabara Ichiro, Liu Fu-Tong, Kaltner Herbert, Gabius Hans-Joachim
Institute of Photobiology, National Academy of Sciences of Belarus, Minsk.
Mol Cell Biochem. 2003 Aug;250(1-2):139-49. doi: 10.1023/a:1024952727159.
Cell surface glycans present docking sites to endogenous lectins. With growing insight into the diversity of lectin families it becomes important to answer the question on the activity profiles of individual family members. Focusing on galectins (beta-galactoside-binding proteins without Ca(2+)-requirement sharing the jelly-roll-like folding pattern), this study was performed to assess the potency of proto-type galectins (galectins-1 and -7 and CG-16) and the chimera-type galectin-3 to elicit selected cell responses by carbohydrate-dependent surface binding and compare the results. The galectins, except for galectin-1, were found to enhance detergent (SDS)-induced hemolysis of human erythrocytes to different degrees. Their ability to confer increased membrane osmofragility thus differs. Aggregation of neutrophils, thymocytes and platelets was induced by the proto-type galectin-1 but not -7, by CG-16 and also galectin-3. Cell-type-specific quantitative differences and the importance of the fine-specificity of the galectin were clearly apparent. In order to detect cellular responses based on galectin binding and bridging of cells the formation of haptenic-sugar-resistant (HSR) intercellular contacts (an indicator of post-binding signaling) was monitored. It was elicited by CG-16 and galectin-1 but not galectin-3, revealing another level at which activities of individual galectins can differ. Acting as potent elicitor of neutrophil aggregation, CG-16-dependent post-binding effects were further analyzed. Carbohydrate-dependent binding to the neutrophils' surface led to a sustained increase of cytoplasmic Ca2+ concentration in a dose-dependent manner. The ability of CG-16 to activate H2O2 generation by human peripheral blood neutrophils was primed by the Ca(2+)-ionophor ionomycin and by cytochalasin B. In a general context, these results emphasize that--besides plant lectins as laboratory tools--animal lectins can trigger cell reaction cascades, implying potential in vivo relevance for the measured activities. Within the family of galectins, the activity profiles depend on the target cell type and the individual galectin. Notably, proto-type galectins do not necessarily share a uniform capacity as elicitor.
细胞表面聚糖为内源性凝集素提供对接位点。随着对凝集素家族多样性的深入了解,回答单个家族成员的活性谱问题变得至关重要。本研究聚焦于半乳糖凝集素(无需Ca(2+)的β-半乳糖苷结合蛋白,具有果冻卷样折叠模式),旨在评估原型半乳糖凝集素(半乳糖凝集素-1、-7和CG-16)以及嵌合型半乳糖凝集素-3通过碳水化合物依赖性表面结合引发特定细胞反应的能力,并比较结果。除半乳糖凝集素-1外,其他半乳糖凝集素均被发现能不同程度地增强去污剂(SDS)诱导的人红细胞溶血。因此,它们赋予膜渗透脆性增加的能力有所不同。原型半乳糖凝集素-1而非-7、CG-16以及半乳糖凝集素-3可诱导中性粒细胞、胸腺细胞和血小板聚集。细胞类型特异性的定量差异以及半乳糖凝集素精细特异性的重要性清晰可见。为了检测基于半乳糖凝集素结合和细胞桥接的细胞反应,监测了半抗原糖抗性(HSR)细胞间接触的形成(结合后信号传导的指标)。它由CG-16和半乳糖凝集素-1引发,但不由半乳糖凝集素-3引发,揭示了单个半乳糖凝集素活性可能不同的另一个层面。作为中性粒细胞聚集的有效诱导剂,对CG-16依赖性结合后效应进行了进一步分析。碳水化合物依赖性与中性粒细胞表面的结合导致细胞质Ca2+浓度以剂量依赖性方式持续增加。CG-16激活人外周血中性粒细胞产生H2O2的能力由Ca(2+)离子载体离子霉素和细胞松弛素B引发。总体而言,这些结果强调,除了植物凝集素作为实验室工具外,动物凝集素也可触发细胞反应级联,这意味着所测活性在体内可能具有相关性。在半乳糖凝集素家族中,活性谱取决于靶细胞类型和单个半乳糖凝集素。值得注意的是,原型半乳糖凝集素不一定具有作为诱导剂的统一能力。