MORPHOLOGICAL-CHANGES OF HUMAN MYELOID-LEUKEMIA K562 CELLS BY A PROTEIN PHOSPHATASE INHIBITOR, TAUTOMYCIN

被引:28
作者
MAGAE, J
OSADA, H
FUJIKI, H
SAIDO, TC
SUZUKI, K
NAGAI, K
YAMASAKI, M
ISONO, K
机构
[1] INST PHYS & CHEM RES,ANTIBIOT LAB,WAKO,SAITAMA 35101,JAPAN
[2] NATL CANC CTR,RES INST,DIV CANC PREVENT,CHUO KU,TOKYO 104,JAPAN
[3] TOKYO METROPOLITAN INST MED SCI,DEPT MOLEC BIOL,BUNKYO KU,TOKYO 113,JAPAN
[4] UNIV TOKYO,DEPT AGR CHEM,MICROBIOL LAB,BUNKYO KU,TOKYO 113,JAPAN
来源
PROCEEDINGS OF THE JAPAN ACADEMY SERIES B-PHYSICAL AND BIOLOGICAL SCIENCES | 1990年 / 66卷 / 10期
关键词
TAUTOMYCIN; PROTEIN PHOSPHATASE; OKADAIC ACID;
D O I
10.2183/pjab.66.209
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 ; 0710 ; 09 ;
摘要
An antibiotic, tautomycin induced bled formation and protein phosphorylation of K562 cells as do the protein phosphatase inhibitors, okadaic acid and dinophysistoxin-1. Tautomycin inhibited the specific binding of [H-3]okadaic acid to protein phosphatases. Furthermore, tautomycin inhibited the protein phosphatases isolated from mouse brain. However, tautomycin did not activate the protein kinase C. These results indicate that tautomycin induces bled formation through inhibition of protein phosphatases.
引用
收藏
页码:209 / 212
页数:4
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