EXPRESSION OF THE FMS-LIKE TYROSINE KINASE-4 GENE BECOMES RESTRICTED TO LYMPHATIC ENDOTHELIUM DURING DEVELOPMENT

被引:1166
作者
KAIPAINEN, A
KORHONEN, J
MUSTONEN, T
VANHINSBERGH, VWM
FANG, GH
DUMONT, D
BREITMAN, M
ALITALO, K
机构
[1] NETHERLANDS CENT ORG APPL SCI RES,INST AGEING & VASC RES,GAUBIUS LAB,2300 AK LEIDEN,NETHERLANDS
[2] MT SINAI HOSP,SAMUEL LUNENFELD RES INST,TORONTO,ON M5G 1X5,CANADA
关键词
D O I
10.1073/pnas.92.8.3566
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 [理学]; 0710 [生物学]; 09 [农学];
摘要
We have recently cloned the human fms-like tyrosine kinase 4 gene FLT4, whose protein product is related to two vascular endothelial growth factor receptors FLT1 and KDR/FLK1, Here the expression of FLT4 has been analyzed by in situ hybridization during mouse embryogenesis and in adult human tissues. The FLT4 mRNA signals first became detectable in the angioblasts of head mesenchyme, the cardinal vein, and extraembryonally in the allantois of 8.5 day postcoitus (p.c.) embryos. In 12.5-day p,c, embryos, the FLT4 signal decorated developing venous and presumptive lymphatic endothelia, but arterial endothelia were negative. During later stages of development, FLTI mRNA became restricted to vascular plexuses devoid of red cells, representing developing lymphatic vessels. Only the lymphatic endothelia and some high endothelial venules expressed FLT4 mRNA in adult human tissues. Increased expression occurred in lymphatic sinuses in metastatic lymph nodes and in lymphangioma, Our results suggest that FLT4 is a marker for lymphatic vessels and some high endothelial venules in human adult tissues. They also support the theory on the venous origin of lymphatic vessels.
引用
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页码:3566 / 3570
页数:5
相关论文
共 38 条
[1]
BONTHRON DT, 1986, NUCLEIC ACIDS RES, V141, P7125
[2]
CATORETTI G, 1992, J PATHOL, V168, P357
[3]
COFFIN JD, 1988, DEVELOPMENT, V102, P735
[4]
THE FMS-LIKE TYROSINE KINASE, A RECEPTOR FOR VASCULAR ENDOTHELIAL GROWTH-FACTOR [J].
DEVRIES, C ;
ESCOBEDO, JA ;
UENO, H ;
HOUCK, K ;
FERRARA, N ;
WILLIAMS, LT .
SCIENCE, 1992, 255 (5047) :989-991
[5]
FINNERTY H, 1993, ONCOGENE, V8, P2293
[6]
FLAMME I, 1992, DEVELOPMENT, V116, P435
[7]
ANGIOGENIC FACTORS [J].
FOLKMAN, J ;
KLAGSBRUN, M .
SCIENCE, 1987, 235 (4787) :442-447
[8]
FOLKMAN J, 1992, J BIOL CHEM, V267, P10931
[9]
Folkman J, 1992, Semin Cancer Biol, V3, P65
[10]
GENESER F, 1986, TXB HISTOLOGY, P333