A possible immunosuppressant, cycloprodigiosin hydrochloride, obtained from Pseudoalteromonas denitrificans

被引:89
作者
Kawauchi, K
Shibutani, K
Yagisawa, H
Kamata, H
Nakatsuji, S
Anzai, H
Yokoyama, Y
Ikegami, Y
Moriyama, Y
Hirata, H
机构
[1] HIMEJI INST TECHNOL,FAC SCI,DEPT LIFE SCI,KAMIGORI,HYOGO 67812,JAPAN
[2] HIMEJI INST TECHNOL,FAC SCI,DEPT MAT SCI,KAMIGORI,HYOGO 67812,JAPAN
[3] AKO KASEI CO LTD,DEPT TECHNOL,AKO,HYOGO 67801,JAPAN
[4] OSAKA UNIV,INST SCI & IND RES,IBARAKI,OSAKA 567,JAPAN
关键词
D O I
10.1006/bbrc.1997.7186
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
Cycloprodigiosin hydrochloride (cPrG.HCl), a member of the prodigiosin family, is a red pigment obtained from the marine bacterium Pseudoalteromonas denitrificans. cPrG.HCl markedly suppressed H-3-thymidine incorporation by concanavalin A stimulated murine splenocytes but had Little effect on lipopolysaccharide dependent H-3-thymidine incorporation, indicating that cPrG.HCl acts as a selective inhibitor of T cell proliferation in the same way as other members of the prodigiosin family. cPrG.HCl inhibited the proliferation of the PMA stimulated Jurkat cells through an apoptotic process. Intriguingly, cPrG.HCl inhibited the H+ translocation by vacuolar type ATPase in chromaffin granule membranes without any effect on either its ATPase activity nor on the membrane conductance of phospholipid bilayers, suggesting that cPrG.HCl selectively uncouples H+ translocation from the ATPase reaction rather than acting as a non-specific ionophore. Since crystalline cPrG.HCl is highly stable, it raises the possibility of its therapeutic use as an immunosuppressant. (C) 1991 Academic Press.
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页码:543 / 547
页数:5
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