Hematopoietic progenitor cell rolling in bone marrow microvessels: Parallel contributions by endothelial selectins and vascular cell adhesion molecule 1
被引:344
作者:
Mazo, IB
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机构:Ctr Blood Res, Boston, MA 02115 USA
Mazo, IB
Gutierrez-Ramos, JC
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机构:Ctr Blood Res, Boston, MA 02115 USA
Gutierrez-Ramos, JC
Frenette, PS
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机构:Ctr Blood Res, Boston, MA 02115 USA
Frenette, PS
Hynes, RO
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机构:Ctr Blood Res, Boston, MA 02115 USA
Hynes, RO
Wagner, DD
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机构:Ctr Blood Res, Boston, MA 02115 USA
Wagner, DD
von Andrian, UH
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机构:Ctr Blood Res, Boston, MA 02115 USA
von Andrian, UH
机构:
[1] Ctr Blood Res, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Dept Pathol, Boston, MA 02115 USA
[3] Harvard Univ, Sch Med, Dept Med, Boston, MA 02115 USA
[4] Millenium Pharmaceut Inc, Cambridge, MA 02139 USA
[5] MIT, Howard Hughes Med Inst, Cambridge, MA 02139 USA
bone marrow;
selectins;
alpha;
4;
integrin;
intravital microscopy;
homing;
D O I:
10.1084/jem.188.3.465
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
We have used intravital microscopy to study physiologically perfused microvessels in murine bone mallow (BM). BM sinusoids and venules, but not adjacent bone vessels, supported rolling interactions of hematopoietic progenitor cells. Rolling did not involve L-selectin, but was partially reduced in wild-type mice treated with antibodies to P- or E-selectin and in mice that were deficient in these two selectins. Selectin-independent rolling was mediated by alpha 4 integrins, which interacted with endothelial vascular cell adhesion molecule (VCAM)-1. Parallel contribution of the endothelial selectins and VCAM-1 is not known to direct blood cell trafficking to other noninflamed tissues. This combination of constitutively expressed adhesion molecules may thus constitute a BM-specific recruitment pathway for progenitor cells analogous to the vascular addressins that direct selective lymphocyte homing to lymphoid organs.