Collot M, Kalff M, Remacle J
Eur J Cell Biol. 1982 Nov;29(1):34-42.
Cytochrome b5 has been visualized by an immunoferritin labeling in a Golgi preparation. When the Golgi apparatus was first disrupted before labeling, 60% of the profiles were clearly labeled with ferritin. This proportion of labeled vesicles was too high to be explained by contamination from other membranes. When the Golgi structure was maintained during the experimental process, obviously some small vesicles located at the periphery of the Golgi complex were labeled and at least one saccule per Golgi apparatus was labeled but only at the edges. These conclusions were sustained by a quantitative analysis which showed a low but constant labeling of Golgi saccules and tubules and a very high labeling of some small profiles. These results confirm the presence of cytochrome b5 in the Golgi apparatus but stress its heterogeneous distribution; they also sustain the idea of a possible membrane specific shuttle between the ER and the Golgi apparatus by a recycling process suggested by the presence of highly labeled small vesicles found in close vicinity with the cisternae.
通过免疫铁蛋白标记已在高尔基体制剂中观察到细胞色素b5。当在标记前首先破坏高尔基体时,60%的轮廓被铁蛋白清晰标记。这种标记小泡的比例过高,无法用来自其他膜的污染来解释。当在实验过程中保持高尔基体结构时,显然位于高尔基体复合体周边的一些小泡被标记,并且每个高尔基体至少有一个扁平囊被标记,但仅在边缘处。这些结论通过定量分析得到支持,该分析显示高尔基体扁平囊和小管的标记率较低但恒定,而一些小轮廓的标记率非常高。这些结果证实了细胞色素b5在高尔基体中的存在,但强调了其分布的异质性;它们还支持了通过在靠近扁平囊处发现的高度标记的小泡的存在所暗示的回收过程,在内质网和高尔基体之间可能存在膜特异性穿梭的观点。