Leonardi-Essmann Fernando, Emig Michael, Kitamura Yoshihisa, Spanagel Rainer, Gebicke-Haerter Peter J
Central Institute for Mental Health, Department of Psychopharmacology, J5, 68159 Mannheim, Germany.
J Neuroimmunol. 2005 Mar;160(1-2):92-101. doi: 10.1016/j.jneuroim.2004.11.012. Epub 2005 Jan 28.
Fractalkine is the only known member of the CX(3)C-chemokine family, and so is its receptor CX(3)CR1. Fractalkine, typically is expressed by neurons where it is inserted in the plasma membrane ("chemokine on a stalk"). It can, however, be clipped off by a specific enzyme and diffuse into the extracellular space. CX(3)CR1 is primarily expressed by microglia, the phagocytes of the brain. This study was aimed at studying gene expression changes in cultured rat microglia upon fractalkine stimulation using gene chip technology. Six genes turned out to be upregulated, amongst which milk-fat globule EGF factor-8 protein (MFG-E8) was the most surprising, but also the most revealing one. We hypothesize that it serves as a bridging molecule between apoptotic cells (neurons) and microglia. Since the docking to microglia is, in part, mediated by members of the integrin family, six of these molecules have been-post hoc-included in real-time PCR confirmations of chip results. Two of them-integrin alpha(2) and integrin beta(5)-were upregulated as well. These data provide a much closer look into molecular mechanisms involved in apoptosis of neurons and their removal by microglia.
趋化因子是CX(3)C趋化因子家族中唯一已知的成员,其受体CX(3)CR1也是如此。趋化因子通常由神经元表达,并插入质膜中(“柄上的趋化因子”)。然而,它可以被一种特定的酶剪切下来并扩散到细胞外空间。CX(3)CR1主要由小胶质细胞表达,小胶质细胞是大脑中的吞噬细胞。本研究旨在利用基因芯片技术研究趋化因子刺激后培养的大鼠小胶质细胞中的基因表达变化。结果发现有六个基因上调,其中乳脂肪球表皮生长因子8蛋白(MFG-E8)最为惊人,但也是最具启发性的一个。我们假设它作为凋亡细胞(神经元)和小胶质细胞之间的桥梁分子。由于与小胶质细胞的对接部分是由整合素家族成员介导的,因此其中六个分子在事后被纳入芯片结果的实时PCR确认中。其中两个——整合素α(2)和整合素β(5)——也上调了。这些数据让我们更深入地了解了神经元凋亡及其被小胶质细胞清除所涉及的分子机制。