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Fractalkine/CX3CL1: a potential new target for inflammatory diseases.

机译:Fractalkine / CX3CL1:炎性疾病的潜在新靶标。

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摘要

Chemokines are small, chemoattractant proteins that recruit inflammatory cells at the site of inflammation. Because of this, chemokines and their receptors are considered to be therapeutic targets in chronic inflammatory disorders (1). Humans have more than fifty distinct chemokines, small (8-10 kDa) heparin-binding proteins that were identified by their chemotactic activity in bone marrow-derived cells (2). Broadly based on the findings, two types of chemokines exist: 1) inflammatory chemokines, which recruit leukocytes in response to physiological stress, and 2) homeostatic chemokines, which account for basal leukocyte trafficking and the formation of the architecture of secondary lymphoid organs (3, 4). Inflammatory chemokine expression can be elicited by almost any stimulus that alters cellular homeostasis, such as infections and immune disorders (4).
机译:趋化因子是小的趋化因子蛋白,可在炎症部位募集炎症细胞。因此,趋化因子及其受体被认为是慢性炎性疾病的治疗靶点(1)。人类具有五十多种不同的趋化因子,小的(8-10 kDa)肝素结合蛋白,通过在骨髓衍生细胞中的趋化活性来鉴定(2)。广泛地基于该发现,存在两种类型的趋化因子:1)炎症趋化因子,其响应生理压力而募集白细胞; 2)稳态趋化因子,其负责基础白细胞的运输和次级淋巴器官的结构形成(3 ,4)。几乎任何改变细胞稳态的刺激都可以引起炎症趋化因子的表达,例如感染和免疫紊乱(4)。

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