TYROSINE PHOSPHORYLATION OF HUMAN UROKINASE-TYPE PLASMINOGEN-ACTIVATOR

被引:11
作者
BARLATI, S
PARACINI, F
BELLOTTI, D
DEPETRO, G
机构
[1] Division of Biology and Genetics, Department of Biomedical Sciences and Biotechnologies, University of Brescia
关键词
HUMAN UROKINASE-TYPE PA; TYROSINE PHOSPHORYLATION; HT-1080; CELL; TUMOR;
D O I
10.1016/0014-5793(91)80377-F
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
Immunoblotting analysis of purified human urokinase plasminogen activator (u-PA), gives a positive signal when reacted with anti-phosphotyrosine monoclonal antibodies (MoAb anti-P-Tyr); competition with omicron-phospho-DL-tyrosine (P-Tyr) but not omicron-phospho-DL-threonine or serine (P-Treo, P- Ser) completely suppresses this signal. Either the 55 kDa u-PA form and the lower M(w) form (33 kDa) derived from the 55 kDa u-PA are Tyr-phosphorylated also the u-PA secreted in the culture media of human fibrosarcoma cells (HT-1080) is phosphorylated in tyrosine as well as u-PA present in tissue extracts of tumors induced in nude mice by HT-1080 cells. These data show that urine purified human u-PA and u-PA produced by human fibrosarcoma cells, in vitro and in vivo, are phosphorylated in tyrosine; furthermore our data show that u-PA is the major Tyr-phosphorylated protein present in these human tumor cells.
引用
收藏
页码:137 / 140
页数:4
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