Gabius S, Gabius H J
Medizinische Universitätsklinik, Abteilung Hämatologie-Onkologie, Göttingen, Federal Republic of Germany.
Blut. 1990 Oct;61(4):232-9. doi: 10.1007/BF01744137.
Intimate cellular contacts and coordinated supply of regulatory factors are required to maintain the still inexplicable dynamic equilibrium of hemopoiesis. To infer the potential participation of protein-carbohydrate interaction in this complex process, human long-term bone marrow cultures were initiated from eleven donors, and the adherent cell layer was characterized enzyme- and immunohistochemically. Utilizing an array of carrier-immobilized carbohydrate ligands and sulfated polysaccharides as probes, specific binding of various constituents of the carbohydrate chains of cellular glycoconjugates to the stromal cells was unmistakably disclosed. Biochemical analysis, employing glycocytologically effective ligands in affinity chromatography, corroborated this result. The extent of binding was markedly lower in the two samples, derived from leukemia patients. Pronounced adaptive responses for this characteristic followed changes in the culture microenvironment that are known to influence qualitative and quantitative aspects of hemopoiesis in vitro, namely omission of hydrocortisone and horse serum or addition of cytokines. Similarly, such adaptive modulation occurred on the level of accessible cell surface receptors, monitored by neoglycoenzymes. These binding sites can be involved in mediation of cellular interactions, as revealed in a model system by the interference of N-acetyl-D-galactosamine in cell adhesion. Overall, the results support the idea that glycobiological recognition may contribute to the functional integrity of the stromal cell layer as well as provide the basis for further analysis.
维持造血过程中仍无法解释的动态平衡需要紧密的细胞接触和调节因子的协调供应。为了推断蛋白质 - 碳水化合物相互作用在这一复杂过程中的潜在参与情况,从11名供体中启动了人类长期骨髓培养,并通过酶学和免疫组织化学方法对贴壁细胞层进行了表征。利用一系列载体固定化的碳水化合物配体和硫酸化多糖作为探针,明确揭示了细胞糖缀合物碳水化合物链的各种成分与基质细胞的特异性结合。在亲和色谱中使用对糖细胞学有效的配体进行的生化分析证实了这一结果。来自白血病患者的两个样本中的结合程度明显较低。对于这一特征,明显的适应性反应跟随培养微环境的变化而发生,已知这些变化会影响体外造血的定性和定量方面,即省略氢化可的松和马血清或添加细胞因子。同样,这种适应性调节发生在可及的细胞表面受体水平,通过新糖酶进行监测。这些结合位点可能参与细胞相互作用的介导,如在模型系统中通过N - 乙酰 - D - 半乳糖胺对细胞粘附的干扰所揭示的那样。总体而言,这些结果支持这样一种观点,即糖生物学识别可能有助于基质细胞层的功能完整性,并为进一步分析提供基础。