6-C-kine (SLC), a lymphocyte adhesion-triggering chemokine expressed by high endothelium, is an agonist for the MIP-3beta receptor CCR7.
6-C-kine (SLC), a lymphocyte adhesion-triggering chemokine expressed by high endothelium, is an agonist for the MIP-3beta receptor CCR7.
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DOI:
10.1083/jcb.141.4.1053
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发表时间:
1998-05-18
期刊:
影响因子:
--
通讯作者:
Butcher EC
中科院分区:
文献类型:
--
作者:
Campbell JJ;Bowman EP;Murphy K;Youngman KR;Siani MA;Thompson DA;Wu L;Zlotnik A;Butcher EC
The β chemokine known as 6-C-kine, secondary lymphoid-tissue chemokine (SLC), TCA4, or Exodus-2 (herein referred to as 6CK/SLC) can trigger rapid integrin-dependent arrest of lymphocytes rolling under physiological shear and is highly expressed by high endothelial venules, specialized vessels involved in lymphocyte homing from the blood into lymph nodes and Peyer's patches. We show that 6CK/SLC is an agonist for the lymphocyte chemoattractant receptor, CCR7 (EBI-1, BLR-2), previously described as a receptor for the related β chemokine MIP-3β (ELC or Exodus-3). Moreover, 6CK/SLC and MIP-3β attract the same major populations of circulating lymphocytes, including naive and memory T cells > B cells (but not natural killer cells); desensitization to MIP-3β inhibits lymphocyte chemotaxis to 6CK/SLC but not to the α chemokine SDF-1 (stromal cell–derived factor); and 6CK/SLC competes for MIP-3β binding to resting mouse lymphocytes. The findings suggest that the majority of circulating lymphocytes respond to 6CK/SLC and MIP-3β in large part through their common receptor CCR7 and that these molecules may be important mediators of physiological lymphocyte recirculation in vivo.
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影响因子:
56.9
作者:
Campbell, JJ;Hedrick, J;Butcher, EC
通讯作者:
Butcher, EC
影响因子:
56.9
作者:
Butcher, EC;Picker, LJ
通讯作者:
Picker, LJ
DOI:
10.1084/jem.184.3.963
发表时间:
1996-09-01
期刊:
The Journal of experimental medicine
影响因子:
--
作者:
Loetscher M;Gerber B;Loetscher P;Jones SA;Piali L;Clark-Lewis I;Baggiolini M;Moser B
通讯作者:
Moser B
影响因子:
56.9
作者:
DAWSON, PE;MUIR, TW;KENT, SBH
通讯作者:
KENT, SBH
影响因子:
4.8
作者:
Nagira, M;Imai, T;Yoshie, O
通讯作者:
Yoshie, O