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CC趋化因子对血管重塑的不依赖白细胞的作用

Leukocyte-Independent Effects of CC-Chemokines on Vascular Remodeling.

作者信息

Paccosi Sara, Parenti Astrid

机构信息

Department of Health Sciences, University of Florence, Florence, Italy.

出版信息

Curr Pharm Biotechnol. 2018;19(9):715-727. doi: 10.2174/1389201019666181017161447.

DOI:10.2174/1389201019666181017161447
PMID:30332947
Abstract

BACKGROUND

Vascular remodeling is an alteration in the structure of vessels in response to injury or hemodynamic changes. Disturbance of the structural and functional integrity of the endothelial cell layer can be observed in vascular remodeling associated with inflammation. Chemokines have been implicated in a wide range of diseases with prominent inflammatory components, and also in vascular remodeling. Among them, CC-chemokines are of great interest. They act through conventional CC-chemokine receptors (CCRs), widely expressed by leucocytes which are attracted to sites of chronic inflammation. However, many experimental data show that CCRs are expressed by vascular cells, suggesting a direct, leukocyte-independent effect on vascular remodeling.

OBJECTIVE

Here, we discuss the role of CC-chemokines in atherosclerosis, angiogenesis, restenosis and renal dysfunction through direct activation of endothelial cells, endothelial progenitors, vascular smooth muscle cells, platelets, erythrocytes, mesangial cells and fibroblasts.

RESULTS

The pathophysiological role of CC-chemokines has become more interesting since the discovery of the atypical chemokine receptor (ACKR) subfamily, that does not couple with G proteins and fails to transmit conventional intracellular signals. It has been demonstrated to be a chemokine scavenger or decoy receptor with a role in the regulation of acute inflammatory responses.

CONCLUSION

At the vascular level, ACKRs are expressed by endothelial cells and endothelial lymphatic cells that seem to regulate angio- and lymph-angiogenesis. Pleiotropic effects of CC-chemokines on vascular wall cells and leukocytes increase their importance in vascular remodeling and suggest new drugs to counteract vascular dysfunction.

摘要

背景

血管重塑是血管结构响应损伤或血流动力学变化而发生的改变。在与炎症相关的血管重塑过程中,可观察到内皮细胞层结构和功能完整性受到干扰。趋化因子与多种具有显著炎症成分的疾病有关,也与血管重塑有关。其中,CC趋化因子备受关注。它们通过传统的CC趋化因子受体(CCR)发挥作用,这些受体在被吸引至慢性炎症部位的白细胞中广泛表达。然而,许多实验数据表明CCR也在血管细胞中表达,提示其对血管重塑具有直接的、不依赖白细胞的作用。

目的

在此,我们通过直接激活内皮细胞、内皮祖细胞、血管平滑肌细胞、血小板、红细胞、系膜细胞和成纤维细胞,探讨CC趋化因子在动脉粥样硬化、血管生成、再狭窄和肾功能不全中的作用。

结果

自发现非典型趋化因子受体(ACKR)亚家族以来,CC趋化因子的病理生理作用变得更具吸引力,该亚家族不与G蛋白偶联,无法传递传统的细胞内信号。它已被证明是一种趋化因子清除剂或诱饵受体,在调节急性炎症反应中发挥作用。

结论

在血管水平,ACKR在内皮细胞和内皮淋巴管细胞中表达,似乎调节血管生成和淋巴管生成。CC趋化因子对血管壁细胞和白细胞的多效性作用增加了它们在血管重塑中的重要性,并提示了对抗血管功能障碍的新药。

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