Methods to study lymphatic vessel integrins

被引:20
作者
Garmy-Susini, Barbara [1 ]
Makale, Milan
Fuster, Mark
Varner, Judith A.
机构
[1] Univ Calif San Diego, Moores UCSD Canc Ctr, La Jolla, CA 92093 USA
[2] Univ Calif San Diego, Dept Med, San Diego, CA 92103 USA
来源
INTEGRINS | 2007年 / 426卷
关键词
D O I
10.1016/S0076-6879(07)26018-5
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The lymphatic system plays a key role in the drainage of fluids and proteins from tissues and in the trafficking of immune cells throughout the body. Comprised of a network of capillaries, collecting vessels, and lymph nodes, the lymphatic system plays a role in the metastasis of tumor cells to distant parts of the body. Tumors induce lymphangiogenesis, the growth of new lymphatic vessels, in the peritumoral space and also within tumors and lymph nodes. Tumor lymphangiogenesis has been shown to play a role in promoting tumor metastasis. As mediators of lymphatic endothelial cell adhesion, migration, and survival, integrins play key roles in the regulation of lymphangiogenesis. Recent studies indicate that select integrins promote lymphangiogenesis during development and disease and that inhibitors or loss of expression of these integrins can block lymphangiogenesis. In this report, we describe methods to isolate and culture murine and human lymphatic endothelial cells as well as methods to analyze the expression of integrins on these cells. We also show how to assess integrin-mediated adhesion, migration, and tube formation in vitro. We demonstrate how to evaluate integrin function during lymphangiogenesis in a variety of animal models in vivo. Additionally, we show how to study lymphangiogenesis using intravital microscopy.
引用
收藏
页码:415 / 438
页数:24
相关论文
共 35 条
[1]   VE-cadherin-Cre-recombinase transgenic mouse: A tool for lineage analysis and gene deletion in endothelial cells [J].
Alva, JA ;
Zovein, AC ;
Monvoisin, A ;
Murphy, T ;
Salazar, A ;
Harvey, NL ;
Carmeliet, P ;
Iruela-Arispe, ML .
DEVELOPMENTAL DYNAMICS, 2006, 235 (03) :759-767
[2]  
Ando T., 2005, Lymphatic Research and Biology, V3, P105, DOI 10.1089/lrb.2005.3.105
[3]  
Bando H, 2006, ONCOL REP, V15, P653
[4]   LYVE-1, a new homologue of the CD44 glycoprotein, is a lymph-specific receptor for hyaluronan [J].
Banerji, S ;
Ni, J ;
Wang, SX ;
Clasper, S ;
Su, J ;
Tammi, R ;
Jones, M ;
Jackson, DG .
JOURNAL OF CELL BIOLOGY, 1999, 144 (04) :789-801
[5]   High correlation of whole-body red fluorescent protein imaging and magnetic resonance imaging on an orthotopic model of pancreatic cancer [J].
Bouvet, M ;
Spernyak, J ;
Katz, MH ;
Mazurchuk, RV ;
Takimoto, S ;
Bernacki, R ;
Rustum, YM ;
Moossa, AR ;
Hoffman, RM .
CANCER RESEARCH, 2005, 65 (21) :9829-9833
[6]  
Bouvet M, 2002, CANCER RES, V62, P1534
[7]   REQUIREMENT OF VASCULAR INTEGRIN ALPHA(V)BETA(3) FOR ANGIOGENESIS [J].
BROOKS, PC ;
CLARK, RAF ;
CHERESH, DA .
SCIENCE, 1994, 264 (5158) :569-571
[8]   Tumor lymphangiogenesis predicts melanoma metastasis to sentinel lymph nodes [J].
Dadras, SS ;
Lange-Asschenfeldt, B ;
Velasco, P ;
Nguyen, L ;
Vora, A ;
Muzikansky, A ;
Jahnke, K ;
Hauschild, A ;
Hirakawa, S ;
Mihm, MC ;
Detmar, M .
MODERN PATHOLOGY, 2005, 18 (09) :1232-1242
[9]   DEFINITION OF 2 ANGIOGENIC PATHWAYS BY DISTINCT ALPHA(V) INTEGRINS [J].
FRIEDLANDER, M ;
BROOKS, PC ;
SHAFFER, RW ;
KINCAID, CM ;
VARNER, JA ;
CHERESH, DA .
SCIENCE, 1995, 270 (5241) :1500-1502
[10]   Integrin α4β1-VCAM-1-mediated adhesion between endothelial and mural cells is required for blood vessel maturation [J].
Garmy-Susini, B ;
Jin, H ;
Zhu, YH ;
Sung, RJ ;
Hwang, R ;
Varner, J .
JOURNAL OF CLINICAL INVESTIGATION, 2005, 115 (06) :1542-1551