Therapeutic differentiation and maturation of lymphatic vessels after lymph node dissection and transplantation

被引:292
作者
Tammela, Tuomas
Saaristo, Anne
Holopainen, Tanja
Lyytikkae, Johannes
Kotronen, Anna
Pitkonen, Miia
Abo-Ramadan, Usama
Ylae-Herttuala, Seppo
Petrova, Tatiana V.
Alitalo, Kari
机构
[1] Univ Helsinki, Ludwig Inst Canc Res, Haartman Inst, Biomedicum,Mol Canc Biol Lab, FIN-00014 Helsinki, Finland
[2] Turku Univ, Cent Hosp, Dept Neurol, Expt MRI Lab, FIN-20521 Turku, Finland
[3] Univ Kuopio, AI Virtanen Inst Mol Sci, Dept Biotechnol & Mol Med, FIN-70211 Kuopio, Finland
[4] Univ Helsinki, Biomedicum, Dev & Differentiat Lab, FIN-00014 Helsinki, Finland
关键词
D O I
10.1038/nm1689
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Surgery or radiation therapy of metastatic cancer often damages lymph nodes, leading to secondary lymphedema. Here we show, using a newly established mouse model, that collecting lymphatic vessels can be regenerated and fused to lymph node transplants after lymph node removal. Treatment of lymph node-excised mice with adenovirally delivered vascular endothelial growth factor-C (VEGF-C) or VEGF-D induced robust growth of the lymphatic capillaries, which gradually underwent intrinsic remodeling, differentiation and maturation into functional collecting lymphatic vessels, including the formation of uniform endothelial cell-cell junctions and intraluminal valves. The vessels also reacquired pericyte contacts, which downregulated lymphatic capillary markers during vessel maturation. Growth factor therapy improved the outcome of lymph node transplantation, including functional reconstitution of the immunological barrier against tumor metastasis. These results show that growth factor-induced maturation of lymphatic vessels is possible in adult mice and provide a basis for future therapy of lymphedema.
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收藏
页码:1458 / 1466
页数:9
相关论文
共 50 条
[1]   Lymphangiogenesis in development and human disease [J].
Alitalo, K ;
Tammela, T ;
Petrova, TV .
NATURE, 2005, 438 (7070) :946-953
[2]   Endothelial/pericyte interactions [J].
Armulik, A ;
Abramsson, A ;
Betsholtz, C .
CIRCULATION RESEARCH, 2005, 97 (06) :512-523
[3]   Monocyte activation in angiogenesis and collateral growth in the rabbit hindlimb [J].
Arras, M ;
Ito, WD ;
Scholz, D ;
Winkler, B ;
Schaper, J ;
Schaper, W .
JOURNAL OF CLINICAL INVESTIGATION, 1998, 101 (01) :40-50
[4]   Pathogenesis of persistent lymphatic vessel hyperplasia in chronic airway inflammation [J].
Baluk, P ;
Tammela, T ;
Ator, E ;
Lyubynska, N ;
Achen, MG ;
Hicklin, DJ ;
Jeltsch, M ;
Petrova, TV ;
Pytowski, B ;
Stacker, SA ;
Ylä-Herttuala, S ;
Jackson, DG ;
Alitalo, K ;
McDonald, DM .
JOURNAL OF CLINICAL INVESTIGATION, 2005, 115 (02) :247-257
[5]   Functionally specialized junctions between endothelial cells of lymphatic vessels [J].
Baluk, Peter ;
Fuxe, Jonas ;
Hashizume, Hiroya ;
Romano, Talia ;
Lashnits, Erin ;
Butz, Stefan ;
Vestweber, Dietmar ;
Corada, Monica ;
Molendini, Cinzia ;
Dejana, Elisabetta ;
McDonald, Donald M. .
JOURNAL OF EXPERIMENTAL MEDICINE, 2007, 204 (10) :2349-2362
[6]   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
[7]  
BAUMEISTER RG, 1981, LANCET, V1, P147
[8]   Postmastectomy lymphedema - Long-term results following microsurgical lymph node transplantation [J].
Becker, C ;
Assouad, J ;
Riquet, M ;
Hidden, G .
ANNALS OF SURGERY, 2006, 243 (03) :313-315
[9]   PDGF-BB induces intratumoral lymphangiogenesis and promotes lymphatic metastasis [J].
Cao, RH ;
Björndahl, MA ;
Religa, P ;
Clasper, S ;
Garvin, S ;
Galter, D ;
Meister, B ;
Ikomi, F ;
Tritsaris, K ;
Dissing, S ;
Ohhashi, T ;
Jackson, DG ;
Cao, YH .
CANCER CELL, 2004, 6 (04) :333-345
[10]   Incidence and risk of arm oedema following treatment for breast cancer: a three-year follow-up study [J].
Clark, B ;
Sitzia, J ;
Harlow, W .
QJM-AN INTERNATIONAL JOURNAL OF MEDICINE, 2005, 98 (05) :343-348