Maciejewski-Lenoir D, Chen S, Feng L, Maki R, Bacon K B
Neurocrine Biosciences Inc., San Diego, CA 92121, USA.
J Immunol. 1999 Aug 1;163(3):1628-35.
Molecular analyses of the chemokine fractalkine and its receptor CX3C-R1 in the rat brain have revealed a striking polarization: fractalkine is expressed constitutively in neurons and is up-regulated by TNF-alpha and IL-1beta in astrocytes. Expression of its specific receptor, CX3C-R1, is restricted to astrocytes and microglia. We have analyzed the functional correlates of this expression and demonstrate that fractalkine induces microglial cell migration and activation. However, the activity of this chemokine on astrocytes may also be highly relevant in inducing astrocyte-microglia cell interactions through cytokine/mediator release leading to microglial activation.
对大鼠脑中趋化因子fractalkine及其受体CX3C-R1的分子分析显示出一种显著的极化现象:fractalkine在神经元中组成性表达,并在星形胶质细胞中被肿瘤坏死因子-α和白细胞介素-1β上调。其特异性受体CX3C-R1的表达仅限于星形胶质细胞和小胶质细胞。我们分析了这种表达的功能相关性,并证明fractalkine可诱导小胶质细胞迁移和激活。然而,这种趋化因子对星形胶质细胞的活性在通过细胞因子/介质释放诱导星形胶质细胞-小胶质细胞相互作用从而导致小胶质细胞激活方面可能也高度相关。