Tumor cell α3β1 integrin and vascular laminin-5 mediate pulmonary arrest and metastasis

被引:153
作者
Wang, H
Fu, WL
Im, JH
Zhou, ZY
Santoro, SA
Iyer, V
DiPersio, CM
Yu, QC
Quaranta, V
Al-Medhi, A
Muschel, RJ
机构
[1] Childrens Hosp Philadelphia, Dept Pathol, Philadelphia, PA 19104 USA
[2] Univ Penn, Dept Pathol, Philadelphia, PA 19104 USA
[3] Vanderbilt Univ, Dept Pathol, Nashville, TN 37322 USA
[4] Vanderbilt Univ, Dept Canc Biol, Nashville, TN 37322 USA
[5] Albany Med Coll, Dept Cell Biol, Albany, NY 12208 USA
[6] Univ S Alabama, Dept Pharmacol, Mobile, AL 36688 USA
关键词
metastasis; tumor cell; integrin; laminin; vessel;
D O I
10.1083/jcb.200309112
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Arrest of circulating tumor cells in distant organs is required for hematogenous metastasis, but the tumor cell surface molecules responsible have not been identified. Here, we show that the tumor cell alpha(3)beta(1), integrin makes an important contribution to arrest in the lung and to early colony formation. These analyses indicated that pulmonary arrest does not occur merely due to size restriction, and raised the question of how the tumor cell 041 integrin contacts its best-defined ligand, laminin (LN)-5, a basement membrane (BM) component. Further analyses revealed that LN-5 is available to the tumor cell in preexisting patches of exposed BM in the pulmonary vasculature. The early arrest of tumor cells in the pulmonary vasculature through interaction of alpha(3)beta(1) integrin with LN-5 in exposed BM provides both a molecular and a structural basis for cell arrest during pulmonary metastasis.
引用
收藏
页码:935 / 941
页数:7
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