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Rab1 defines a novel pathway connecting the pre-Golgi intermediate compartment with the cell periphery

机译:Rab1定义了一条新的途径,将前高尔基体中间腔与细胞外围连接

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The function of the pre-Golgi intermediate compartment (1C) and its relationship with the endoplasmic reticulum (ER) and Golgi remain only partially understood. Here, we report striking segregation of IC domains in polarized PC12 cells that develop neurite-like processes. Differentiation involves expansion of the IC and movement of Rab1-containing tubules to the growth cones of the neurites, whereas p58- and COPI-positive IC elements, like rough ER and Golgi, remain in the cell body. Exclusion of Rab1 effectors p115 and GM130 from the neurites further indicated that the centrifugal, Rab1-mediated pathway has functions that are not directly related to ER-to-Golgi trafficking. Disassembly of COPI coats did not affect this pathway but resulted in missorting of p58 to the neurites. Live cell imaging showed that green fluorescent protein (GFP)-Rab1A-containing IC elements move bidirectionally both within the neurites and cell bodies, interconnecting different ER exit sites and the cis-Golgi region. Moreover, in nonpolarized cells GFP-Rab1A-positive tubules moved centrifugally towards the cell cortex. Hydroxymethylglutaryl-CoA reductase, the key enzyme of cholesterol biosynthesis, colocalized with slowly sedimenting, Rab1-enriched membranes when the IC subdomains were separated by velocity sedimentation. These results reveal a novel pathway directly connecting the IC with the cell periphery and suggest that this Rab1-mediated pathway is linked to the dynamics of smooth ER.
机译:高尔基前中间区室(1C)的功能及其与内质网(ER)和高尔基体的关系仍然只有部分了解。在这里,我们报告了极化的PC12细胞中发生神经突样过程的IC域惊人的分离。分化涉及IC的膨胀和含Rab1的小管向神经突生长锥的运动,而p58和COPI阳性的IC元素(如粗糙的ER和Golgi)则保留在细胞体内。从神经突中排除Rab1效应子p115和GM130进一步表明,离心的Rab1介导的途径具有与ER到高尔基体运输不直接相关的功能。拆卸COPI涂层不会影响该途径,但会导致p58与神经突发生错配。活细胞成像显示,含有绿色荧光蛋白(GFP)-Rab1A的IC元件在神经突和细胞体内双向移动,将不同的ER出口位点和顺式高尔基体区域相互连接。此外,在非极化细胞中,GFP-Rab1A阳性小管向细胞皮质离心移动。羟甲基戊二酰辅酶A还原酶是胆固醇生物合成的关键酶,当通过速度沉淀分离IC子域时,与缓慢沉淀的Rab1富集膜共定位。这些结果揭示了一种直接将IC与细胞外围连接的新颖途径,并表明该Rab1介导的途径与平滑内质网的动力学有关。

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