Cook D N, Chen S C, Sullivan L M, Manfra D J, Wiekowski M T, Prosser D M, Vassileva G, Lira S A
Department of Immunology, Schering-Plough Research Institute, Kenilworth, New Jersey 07033 USA.
Mol Cell Biol. 2001 May;21(9):3159-65. doi: 10.1128/MCB.21.9.3159-3165.2001.
Fractalkine (CX(3)CL1) is the first described chemokine that can exist either as a soluble protein or as a membrane-bound molecule. Both forms of fractalkine can mediate adhesion of cells expressing its receptor, CX(3)CR1. This activity, together with its expression on endothelial cells, suggests that fractalkine might mediate adhesion of leukocytes to the endothelium during inflammation. Fractalkine is also highly expressed in neurons, and its receptor, CX(3)CR1, is expressed on glial cells. To determine the biologic role of fractalkine, we used targeted gene disruption to generate fractalkine-deficient mice. These mice did not exhibit overt behavioral abnormalities, and histologic analysis of their brains did not reveal any gross changes compared to wild-type mice. In addition, these mice had normal hematologic profiles except for a decrease in the number of blood leukocytes expressing the cell surface marker F4/80. The cellular composition of their lymph nodes did not differ significantly from that of wild-type mice. Similarly, the responses of fractalkine(-/-) mice to a variety of inflammatory stimuli were indistinguishable from those of wild-type mice.
趋化因子(CX(3)CL1)是首个被描述的既可以以可溶性蛋白形式存在,也可以以膜结合分子形式存在的趋化因子。趋化因子的这两种形式都能介导表达其受体CX(3)CR1的细胞的黏附。这种活性,连同其在内皮细胞上的表达,表明趋化因子可能在炎症过程中介导白细胞与内皮的黏附。趋化因子在神经元中也高度表达,其受体CX(3)CR1在胶质细胞上表达。为了确定趋化因子的生物学作用,我们使用靶向基因敲除技术培育出趋化因子缺陷小鼠。这些小鼠没有表现出明显的行为异常,与野生型小鼠相比,对它们大脑的组织学分析也没有发现任何明显变化。此外,这些小鼠除了表达细胞表面标志物F4/80的血液白细胞数量减少外,血液学指标正常。它们淋巴结的细胞组成与野生型小鼠没有显著差异。同样,趋化因子缺陷小鼠对各种炎症刺激的反应与野生型小鼠没有区别。