CXCR3-dependent accumulation and activation of perivascular macrophages is necessary for homeostatic arterial remodeling to hemodynamic stresses.
CXCR3-dependent accumulation and activation of perivascular macrophages is necessary for homeostatic arterial remodeling to hemodynamic stresses.
复制标题
DOI:
10.1084/jem.20100098
复制
发表时间:
2010-08-30
期刊:
影响因子:
--
通讯作者:
Tellides G
中科院分区:
文献类型:
--
作者:
Zhou J;Tang PC;Qin L;Gayed PM;Li W;Skokos EA;Kyriakides TR;Pober JS;Tellides G
Sustained changes in blood flow modulate the size of conduit arteries through structural alterations of the vessel wall that are dependent on the transient accumulation and activation of perivascular macrophages. The leukocytic infiltrate appears to be confined to the adventitia, is responsible for medial remodeling, and resolves once hemodynamic stresses have normalized without obvious intimal changes. We report that inward remodeling of the mouse common carotid artery after ligation of the ipsilateral external carotid artery is dependent on the chemokine receptor CXCR3. Wild-type myeloid cells restored flow-mediated vascular remodeling in CXCR3-deficient recipients, adventitia-infiltrating macrophages of Gr1low resident phenotype expressed CXCR3, the perivascular accumulation of macrophages was dependent on CXCR3 signaling, and the CXCR3 ligand IP-10 was sufficient to recruit monocytes to the adventitia. CXCR3 also contributed to selective features of macrophage activation required for extracellular matrix turnover, such as production of the transglutaminase factor XIII A subunit. Human adventitial macrophages displaying a CD14+/CD16+ resident phenotype, but not circulating monocytes, expressed CXCR3, and such cells were more frequent at sites of disturbed flow. Our observations reveal a CXCR3-dependent accumulation and activation of perivascular macrophages as a necessary step in homeostatic arterial remodeling triggered by hemodynamic stress in mice and possibly in humans as well.
登录
查看更多内容
影响因子:
3.7
作者:
Gratchev, A;Kzhyshkowska, J;Goerdt, S
通讯作者:
Goerdt, S
影响因子:
20.1
作者:
Bakker, Erik N. T. P.;Pistea, Adrian;VanBavel, Ed
通讯作者:
VanBavel, Ed
DOI:
10.1084/jem.192.10.1515
发表时间:
2000-11-20
期刊:
The Journal of experimental medicine
影响因子:
--
作者:
Hancock WW;Lu B;Gao W;Csizmadia V;Faia K;King JA;Smiley ST;Ling M;Gerard NP;Gerard C
通讯作者:
Gerard C
DOI:
10.1084/jem.20052205
发表时间:
2006-05-15
期刊:
The Journal of experimental medicine
影响因子:
--
作者:
通讯作者:
--
影响因子:
4.6
作者:
le Noble, F;Moyon, D;Eichmann, A
通讯作者:
Eichmann, A