趋化因子受体
CCL13型
趋化因子受体
CX3CR1型
CCR1
CCR3
CCR10
CXCL2型
CCL21型
C-C趋化因子受体6型
趋化因子受体
生物
CCR2型
趋化因子
XCL2型
细胞生物学
受体
CX3CL1型
CXCL5型
免疫学
炎症
遗传学
作者
Martin E. Dorf,Michael A. Berman,Shinsuke Tanabe,M. Heesen,Yi Luo
标识
DOI:10.1016/s0165-5728(00)00371-4
摘要
Multiple lines of evidence are presented characterizing the functional expression of chemokine receptors CXCR4, CCR1, CCR5, and CX3CR1 on astrocytes. Most of these receptors are expressed at low levels and may only be detectable on a subset of cells during disease or following cytokine induction. The expression of CXCR2, CCR2, CCR3, CCR10, CCR11, and several orphan receptors associated with HIV-1 infection has also been proposed. The appearance of several chemokine receptors implies a wider role for chemokines in the regulation of central nervous system functions. Available evidence indicates that selected chemokines induce further chemokine synthesis in astrocytes providing a mechanism to amplify inflammatory responses in the central nervous system.
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