Feng Yan, Jadhav Ashutosh P, Rodighiero Chiara, Fujinaga Yukako, Kirchhausen Tomas, Lencer Wayne I
Department of Cell Biology, Institute of Chemistry and Cell Biology, Harvard Medical School, Boston, Massachusetts 02115, USA.
EMBO Rep. 2004 Jun;5(6):596-601. doi: 10.1038/sj.embor.7400152. Epub 2004 May 21.
Cholera toxin (CT) follows a glycolipid-dependent entry pathway from the plasma membrane through the trans-Golgi network (TGN) to the endoplasmic reticulum (ER) where it is retro-translocated into the cytosol to induce toxicity. Whether access to the Golgi apparatus is necessary for transport to the ER is not known. Exo2 is a small chemical that rapidly blocks anterograde traffic from the ER to the Golgi and selectively disrupts the Golgi apparatus but not the TGN. Here we use Exo2 to determine the role of the Golgi apparatus in CT trafficking. We find that under the condition of complete Golgi ablation by Exo2, CT reaches the TGN and moves efficiently into the ER without loss in toxicity. We propose that even in the absence of Exo2 the glycolipid pathway that carries the toxin from plasma membrane into the ER bypasses the Golgi apparatus entirely.
霍乱毒素(CT)遵循一条从质膜经反式高尔基体网络(TGN)到内质网(ER)的糖脂依赖性进入途径,在那里它被逆向转运到细胞质溶胶中以诱导毒性。高尔基体对于转运至内质网是否必要尚不清楚。Exo2是一种小分子化学物质,它能迅速阻断从内质网到高尔基体的顺行运输,并选择性地破坏高尔基体而不影响TGN。在这里,我们使用Exo2来确定高尔基体在CT转运中的作用。我们发现,在Exo2完全消融高尔基体的条件下,CT能够到达TGN并有效地进入内质网,且毒性没有损失。我们提出,即使在没有Exo2的情况下,将毒素从质膜转运到内质网的糖脂途径也完全绕过了高尔基体。