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一种可能的免疫抑制剂——盐酸环丙基灵,从反硝化假交替单胞菌中获得。

A possible immunosuppressant, cycloprodigiosin hydrochloride, obtained from Pseudoalteromonas denitrificans.

作者信息

Kawauchi K, Shibutani K, Yagisawa H, Kamata H, Nakatsuji S, Anzai H, Yokoyama Y, Ikegami Y, Moriyama Y, Hirata H

机构信息

Department of Life Science, Faculty of Science, Himeji Institute of Technology, Hyogo, Japan.

出版信息

Biochem Biophys Res Commun. 1997 Aug 28;237(3):543-7. doi: 10.1006/bbrc.1997.7186.

Abstract

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 3H-thymidine incorporation by concanavalin A stimulated murine splenocytes but had little effect on lipopolysaccharide dependent 3H-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.

摘要

盐酸环丙基灵菌红素(cPrG.HCl)是灵菌红素家族的一员,是一种从海洋反硝化假交替单胞菌中获得的红色色素。cPrG.HCl显著抑制伴刀豆球蛋白A刺激的小鼠脾细胞掺入3H-胸腺嘧啶核苷,但对脂多糖依赖的3H-胸腺嘧啶核苷掺入影响很小,这表明cPrG.HCl与灵菌红素家族的其他成员一样,作为T细胞增殖的选择性抑制剂发挥作用。cPrG.HCl通过凋亡过程抑制佛波酯(PMA)刺激的Jurkat细胞的增殖。有趣的是,cPrG.HCl抑制嗜铬粒细胞膜中液泡型ATP酶的H+转运,而对其ATP酶活性和磷脂双层膜电导均无影响,这表明cPrG.HCl选择性地使H+转运与ATP酶反应解偶联,而不是作为一种非特异性离子载体。由于结晶态的cPrG.HCl高度稳定,因此增加了其作为免疫抑制剂用于治疗的可能性。

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