Relman D, Tuomanen E, Falkow S, Golenbock D T, Saukkonen K, Wright S D
Department of Microbiology and Immunology, Stanford University, California 94305.
Cell. 1990 Jun 29;61(7):1375-82. doi: 10.1016/0092-8674(90)90701-f.
During the course of whooping cough, Bordetella pertussis interacts with alveolar macrophages and other leukocytes on the respiratory epithelium. We report here mechanisms by which these bacteria adhere to human macrophages in vitro. Whole bacteria adhere by means of two proteins, filamentous hemagglutinin (FHA) and pertussis toxin, either of which is sufficient to mediate adherence. FHA interacts with two classes of molecules on macrophages, galactose-containing glycoconjugates and the integrin CR3 (alpha M beta 2, CD11b/CD18). The interaction between CR3 and FHA involves recognition of the Arg-Gly-Asp (RGD) sequence at positions 1097-1099 in FHA. This study demonstrates that bacterial adherence can be based on the interaction of a bacterial adhesin RGD sequence with an integrin and that bacterial adhesins can have multiple binding sites characteristic of eukaryotic extracellular matrix proteins.
在百日咳病程中,百日咳博德特氏菌与呼吸道上皮的肺泡巨噬细胞及其他白细胞相互作用。我们在此报告这些细菌在体外黏附人巨噬细胞的机制。完整细菌借助两种蛋白质丝状血凝素(FHA)和百日咳毒素进行黏附,其中任何一种都足以介导黏附。FHA与巨噬细胞上的两类分子相互作用,即含半乳糖的糖缀合物和整合素CR3(αMβ2,CD11b/CD18)。CR3与FHA之间的相互作用涉及对FHA中第1097 - 1099位精氨酸 - 甘氨酸 - 天冬氨酸(RGD)序列的识别。本研究表明,细菌黏附可基于细菌黏附素RGD序列与整合素的相互作用,并且细菌黏附素可具有真核细胞外基质蛋白特有的多个结合位点。