Denker S P, McCaffery J M, Palade G E, Insel P A, Farquhar M G
Division of Cellular and Molecular Medicine, University of California, San Diego, La Jolla, 92093 USA.
J Cell Biol. 1996 Jun;133(5):1027-40. doi: 10.1083/jcb.133.5.1027.
Heterotrimeric G proteins are well known to be involved in signaling via plasma membrane (PM) receptors. Recent data indicate that heterotrimeric G proteins are also present on intracellular membranes and may regulate vesicular transport along the exocytic pathway. We have used subcellular fractionation and immunocytochemical localization to investigate the distribution of G alpha and G beta gamma subunits in the rat exocrine pancreas which is highly specialized for protein secretion. We show that G alpha s, G alpha i3 and G alpha q/11 are present in Golgi fractions which are > 95% devoid of PM. Removal of residual PM by absorption on wheat germ agglutinin (WGA) did not deplete G alpha subunits. G alpha s was largely restricted to TGN-enriched fractions by immunoblotting, whereas G alpha i3 and G alpha q/11 were broadly distributed across Golgi fractions. G alpha s did not colocalize with TGN38 or caveolin, suggesting that G alpha s is associated with a distinct population of membranes. G beta subunits were barely detectable in purified Golgi fractions. By immunofluorescence and immunogold labeling, G beta subunits were detected on PM but not on Golgi membranes, whereas G alpha s and G alpha i3 were readily detected on both Golgi and PM. G alpha and G beta subunits were not found on membranes of zymogen granules. These data indicate that G alpha s, G alpha q/11, and G alpha i3 associate with Golgi membranes independent of G beta subunits and have distinctive distributions within the Golgi stack. G beta subunits are thought to lock G alpha in the GDP-bound form, prevent it from activating its effector, and assist in anchoring it to the PM. Therefore the presence of free G alpha subunits on Golgi membranes has several important functional implications: it suggests that G alpha subunits associated with Golgi membranes are in the active, GTP-bound form or are bound to some other unidentified protein(s) which can substitute for G beta gamma subunits. It further implies that G alpha subunits are tethered to Golgi membranes by posttranslational modifications (e.g., palmitoylation) or by binding to another protein(s).
异源三聚体G蛋白参与质膜(PM)受体介导的信号转导,这一点广为人知。最近的数据表明,异源三聚体G蛋白也存在于细胞内膜上,并可能调节沿外排途径的囊泡运输。我们利用亚细胞分级分离和免疫细胞化学定位技术,研究了大鼠外分泌胰腺中Gα和Gβγ亚基的分布,该胰腺高度特化用于蛋白质分泌。我们发现,Gαs、Gαi3和Gαq/11存在于高尔基体组分中,这些组分中PM的含量不到95%。通过小麦胚凝集素(WGA)吸附去除残留的PM并没有耗尽Gα亚基。通过免疫印迹法,Gαs主要局限于富含反式高尔基体网络(TGN)的组分中,而Gαi3和Gαq/11广泛分布于高尔基体组分中。Gαs与TGN38或小窝蛋白不共定位,这表明Gαs与不同的膜群体相关。在纯化的高尔基体组分中几乎检测不到Gβ亚基。通过免疫荧光和免疫金标记,在PM上检测到了Gβ亚基,但在高尔基体膜上未检测到,而在高尔基体和PM上都很容易检测到Gαs和Gαi3。在酶原颗粒膜上未发现Gα和Gβ亚基。这些数据表明,Gαs、Gαq/11和Gαi3与高尔基体膜结合,不依赖于Gβ亚基,并且在高尔基体堆叠中有独特的分布。Gβ亚基被认为能将Gα锁定在GDP结合形式,阻止其激活效应器,并协助将其锚定到PM上。因此,高尔基体膜上存在游离的Gα亚基具有几个重要的功能意义:这表明与高尔基体膜相关的Gα亚基处于活性的、GTP结合形式,或者与一些其他未鉴定的蛋白质结合,这些蛋白质可以替代Gβγ亚基。这进一步意味着Gα亚基通过翻译后修饰(如棕榈酰化)或与其他蛋白质结合而与高尔基体膜相连。