Tooze J, Hollinshead M
European Molecular Biology Laboratory, Heidelberg, Germany.
Eur J Cell Biol. 1992 Aug;58(2):228-42.
By conventional electron microscopy we observed in mitotic HeLa cells the structures termed Golgi clusters by Lucocq et al. (J. Cell Biol. 104, 865-874 (1987)) and interpreted by them as clusters of vesicular remnants of the Golgi apparatus. Golgi clusters consist of tubular and vesicular profiles about 50 nm in diameter, sometimes associated with larger 250 nm vesicles. When cultures of HeLa cells were incubated for 60 min or 120 min with medium containing high specific activity horseradish peroxidase (HRP) at 10 mg/ml we found that the membrane-bound compartments in the Golgi clusters in mitotic cells contained heavy deposits of HRP reaction product. Neither interphase nor mitotic HeLa cells contain an endogenous peroxidase activity. We concluded that Golgi clusters are an endocytic compartment and confirmed this by showing that Golgi clusters could be labeled with two other endocytic tracers--bovine serum albumin conjugated to colloidal gold and transferrin conjugated to HRP. When cultures were incubated with HRP for only 15 min most of the Golgi clusters in the mitotic cells were either unlabeled or consisted of a mixture of HRP-labeled and unlabeled profiles. Since during mitosis endocytosis is inhibited this was the expected result. When interphase HeLa cells were incubated with Brefeldin A (BFA), the Golgi apparatus disassembled and immunofluorescence microscopy showed that 1,4 beta galactosyltransferase had relocated to the endoplasmic reticulum. When cells in the presence of BFA and lacking the Golgi apparatus were allowed to endocytose HRP and then entered mitosis, typical HRP-labeled Golgi clusters were seen in the mitotic cells. It is therefore highly unlikely that these structures contain membrane derived from the Golgi cisternae that are sensitive to BFA, including in HeLa cells those containing galactosyltransferase. Finally, we found that interphase HeLa cells incubated with okadaic acid contain structures that are morphologically indistinguishable from Golgi clusters but can be labeled by endocytic tracer. Taken together, this evidence indicates that most, if not all, of the membrane-bound compartments in Golgi clusters are tubular early endosomes.
通过传统电子显微镜观察,我们在有丝分裂的海拉细胞中发现了Lucocq等人(《细胞生物学杂志》104卷,865 - 874页(1987年))所称的高尔基体簇结构,并被他们解释为高尔基体的囊泡残余物簇。高尔基体簇由直径约50纳米的管状和囊泡状结构组成,有时与直径更大的250纳米囊泡相关联。当将海拉细胞培养物在含有10毫克/毫升高比活性辣根过氧化物酶(HRP)的培养基中孵育60分钟或120分钟时,我们发现有丝分裂细胞中高尔基体簇内的膜结合区室含有大量HRP反应产物沉淀。间期和有丝分裂期的海拉细胞均不含有内源性过氧化物酶活性。我们得出结论,高尔基体簇是一个内吞区室,并通过证明高尔基体簇可以被另外两种内吞示踪剂标记来证实这一点,这两种示踪剂分别是与胶体金偶联的牛血清白蛋白和与HRP偶联的转铁蛋白。当培养物仅与HRP孵育15分钟时,有丝分裂细胞中的大多数高尔基体簇要么未被标记,要么由HRP标记和未标记结构的混合物组成。由于在有丝分裂期间内吞作用受到抑制,这是预期的结果。当间期海拉细胞与布雷菲德菌素A(BFA)一起孵育时,高尔基体解体,免疫荧光显微镜显示1,4 - β - 半乳糖基转移酶重新定位到内质网。当在存在BFA且缺乏高尔基体的情况下细胞内吞HRP然后进入有丝分裂时,在有丝分裂细胞中可见典型的HRP标记的高尔基体簇。因此,这些结构极不可能含有对BFA敏感的源自高尔基体潴泡的膜,包括海拉细胞中含有半乳糖基转移酶的那些膜。最后,我们发现用冈田酸孵育的间期海拉细胞含有在形态上与高尔基体簇无法区分但可被内吞示踪剂标记的结构。综上所述,这些证据表明,高尔基体簇中大多数(如果不是全部)膜结合区室是管状早期内体。