巨噬细胞炎性蛋白
CCR3
三氯化碳
CCR1
趋化因子
CCL13型
趋化因子受体
炎症
免疫学
趋化因子受体
C-C趋化因子受体6型
促炎细胞因子
巨噬细胞
生物
四氯化碳
化学
生物化学
体外
作者
Marcus Maurer,Esther von Stebut
标识
DOI:10.1016/j.biocel.2003.10.019
摘要
Macrophage inflammatory protein (MIP)-1α was identified 15 years ago as the first of now four members of the MIP-1 CC chemokine subfamily. These proteins termed CCL3 (MIP-1α), CCL4 (MIP-1β), CCL9/10 (MIP-1δ), and CCL15 (MIP-1γ) according to the revised nomenclature for chemokines are produced by many cells, particularly macrophages, dendritic cells, and lymphocytes. MIP-1 proteins, which act via G-protein-coupled cell surface receptors (CCR1, 3, 5), e.g. expressed by lymphocytes and monocytes/macrophages (MΦ), are best known for their chemotactic and proinflammatory effects but can also promote homoeostasis. The encouraging results of preclinical studies in murine models of inflammation, i.e. asthma, arthritis, or multiple sclerosis, have led to the development of potent CCR3 and 5 antagonists, some of which are currently being tested in first clinical trials.
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