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内体到高尔基体的转运受II型α蛋白激酶A调控。

Endosome-to-Golgi transport is regulated by protein kinase A type II alpha.

作者信息

Birkeli Kim Are, Llorente Alicia, Torgersen Maria L, Keryer Guy, Taskén Kjetil, Sandvig Kirsten

机构信息

Institute for Cancer Research, The Norwegian Radium Hospital, Montebello, 0310 Oslo, Norway.

出版信息

J Biol Chem. 2003 Jan 17;278(3):1991-7. doi: 10.1074/jbc.M209982200. Epub 2002 Nov 4.

Abstract

Studies of RII alpha-deficient B lymphoid cells and stable transfectants expressing the type II alpha regulatory subunit (RII alpha) of cAMP-dependent protein kinase (PKA), which is targeted to the Golgi-centrosomal area, reveal that the presence of a Golgi-associated pool of PKA type II alpha mediates a change in intracellular transport of the plant toxin ricin. The transport of ricin from endosomes to the Golgi apparatus, measured as sulfation of a modified ricin (ricin sulf-1), increased in RII alpha-expressing cells when PKA was activated. However, not only endosome-to-Golgi transport, but also retrograde ricin transport to the endoplasmic reticulum (ER), measured as sulfation and N-glycosylation of another modified ricin (ricin sulf-2), seemed to be increased in cells expressing RII alpha in the presence of a cAMP analog, 8-(4-chlorophenylthio)-cAMP. Thus, PKA type II alpha seems to be involved in both endosome-to-Golgi and Golgi-to-ER transport. Because ricin, after being retrogradely transported to the ER, is translocated to the cytosol, where it inhibits protein synthesis, we also investigated the influence of RII alpha expression on ricin toxicity. In agreement with the other data obtained, 8-(4-chlorophenylthio)-cAMP and RII alpha were found to sensitize cells to ricin, indicating an increased transport of ricin to the cytosol. In conclusion, our results demonstrate that transport of ricin from endosomes to the Golgi apparatus and further to the ER is regulated by PKA type II alpha isozyme.

摘要

对缺乏RIIα的B淋巴细胞和稳定转染表达靶向高尔基体-中心体区域的环磷酸腺苷依赖性蛋白激酶(PKA)IIα型调节亚基(RIIα)的研究表明,高尔基体相关的PKA IIα池的存在介导了植物毒素蓖麻毒素细胞内运输的变化。当PKA被激活时,在表达RIIα的细胞中,以修饰蓖麻毒素(蓖麻毒素sulf-1)的硫酸化为指标测定的蓖麻毒素从内体到高尔基体的运输增加。然而,在存在环磷酸腺苷类似物8-(4-氯苯硫基)-环磷酸腺苷的情况下,不仅内体到高尔基体的运输,而且以另一种修饰蓖麻毒素(蓖麻毒素sulf-2)的硫酸化和N-糖基化为指标测定的蓖麻毒素向内质网(ER)的逆行运输,在表达RIIα的细胞中似乎也增加了。因此,PKA IIα型似乎参与了内体到高尔基体和高尔基体到内质网的运输。由于蓖麻毒素在逆行运输到内质网后会转移到细胞质中,在那里它会抑制蛋白质合成,我们还研究了RIIα表达对蓖麻毒素毒性的影响。与获得的其他数据一致,发现8-(4-氯苯硫基)-环磷酸腺苷和RIIα使细胞对蓖麻毒素敏感,表明蓖麻毒素向细胞质的运输增加。总之,我们的结果表明,蓖麻毒素从内体到高尔基体以及进一步到内质网的运输受PKA IIα同工酶调节。

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