Altankov G, Marinova-Mutafchieva L, Nikolaeva N, Penkova R
Central Laboratory of Biophysics, Bulgarian Academy of Sciences.
Methods Find Exp Clin Pharmacol. 1991 May;13(4):263-8.
A quantitative spectrophotometrical method was used to study the adhesive phenotype of lymphocytes from regional lymph nodes of rats with early stage adjuvant-induced arthritis (AA), pretreated or not with cyclophosphamide (CY). The results showed that adhesion of lymphocytes from AA-sensitized lymph nodes to gelatin and collagens (type I, II, III and IV) was enhanced, especially to collagen type II. However, adhesion to fibronectin and to fibrinogen did not differ from adhesion in nontreated rats. Application of CY was found to aggravate AA development and influence the lymphocytes' adhesiveness. Adhesion was inhibited in all cases except to fibrinogen, where it was augmented, compared to the adhesion in both AA and control groups. Relationships between the lymphocyte adhesive phenotype and the expression of histological changes suggest that lymphocyte-matrix interactions could play an important role in the pathogenesis of AA development and the mechanism of CY action.
采用定量分光光度法研究早期佐剂性关节炎(AA)大鼠区域淋巴结淋巴细胞的黏附表型,这些大鼠已用或未用环磷酰胺(CY)预处理。结果显示,来自AA致敏淋巴结的淋巴细胞与明胶和胶原蛋白(I型、II型、III型和IV型)的黏附增强,尤其是与II型胶原蛋白的黏附。然而,与未处理大鼠相比,其与纤连蛋白和纤维蛋白原的黏附无差异。发现应用CY会加重AA的发展并影响淋巴细胞的黏附性。与AA组和对照组的黏附相比,除了与纤维蛋白原的黏附增强外,其他所有情况下黏附均受到抑制。淋巴细胞黏附表型与组织学变化表达之间的关系表明,淋巴细胞与基质的相互作用可能在AA发展的发病机制和CY作用机制中起重要作用。