The Golgi and endoplasmic reticulum remain independent during mitosis in HeLa cells

被引:75
作者
Jesch, SA [1 ]
Linstedt, AD [1 ]
机构
[1] Carnegie Mellon Univ, Dept Biol Sci, Pittsburgh, PA 15213 USA
关键词
D O I
10.1091/mbc.9.3.623
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Partitioning of the mammalian Golgi apparatus during cell division involves disassembly at M-phase. Despite the importance of the disassembly/reassembly pathway in Golgi biogenesis, it remains unclear whether mitotic Golgi breakdown in vivo proceeds by direct vesiculation or involves fusion with the endoplasmic reticulum (ER). To test whether mitotic Golgi is fused with the ER, we compared the distribution of ER and Golgi proteins in interphase and mitotic HeLa cells by immunofluorescence microscopy, velocity gradient fractionation, and density gradient fractionation. While mitotic ER appeared to be a fine reticulum excluded from the region containing the spindle-pole body, mitotic Golgi appeared to be dispersed small vesicles that penetrated the area containing spindle microtubules. After cell disruption,M-phase Golgi was recovered in hive size classes. The major breakdown product, accounting for at least 75% of the Golgi, was a population of 60-nm vesicles that were completely separated from the ER using velocity gradient separation. The minor breakdown product was a larger, more heterogenously sized, membrane population. Double-label fluorescence analysis of these membranes indicated that this portion of mitotic Golgi also lacked detectable ER marker proteins. Therefore we conclude that the ER and Golgi remain distinct at M-phase in HeLa cells. To test whether the 60-nm vesicles might form from the ER at M-phase as the result of a two-step vesiculation pathway involving ER-Golgi fusion followed by Golgi vesicle budding, mitotic cells were generated with fused ER and Golgi by brefeldin A treatment. Upon brefeldin A removal, Golgi vesicles did not emerge from the ER. In contrast, the Golgi readily reformed from similarly treated interphase cells. We conclude that Golgi-derived vesicles remain distinct from the ER in mitotic HeLa cells, and that mitotic cells lack the capacity of interphase cells for Golgi reemergence from the ER. These experiments suggest that mitotic Golgi breakdown proceeds by direct vesiculation independent of the ER.
引用
收藏
页码:623 / 635
页数:13
相关论文
共 47 条
  • [1] THE FORMATION OF GOLGI STACKS FROM VESICULATED GOLGI MEMBRANES REQUIRES 2 DISTINCT FUSION EVENTS
    ACHARYA, U
    JACOBS, R
    PETERS, JM
    WATSON, N
    FARQUHAR, MG
    MALHOTRA, V
    [J]. CELL, 1995, 82 (06) : 895 - 904
  • [2] RECONSTITUTION OF VESICULATED GOLGI MEMBRANES INTO STACKS OF CISTERNAE - REQUIREMENT OF NSF IN STACK FORMATION
    ACHARYA, U
    MCCAFFERY, JM
    JACOBS, R
    MALHOTRA, V
    [J]. JOURNAL OF CELL BIOLOGY, 1995, 129 (03) : 577 - 589
  • [3] ANHQUYEN L, 1994, J BIOL CHEM, V269, P7514
  • [4] ANALYSIS OF THE SUBSTRATE BINDING-SITES OF HUMAN GALACTOSYLTRANSFERASE BY PROTEIN ENGINEERING
    AOKI, D
    APPERT, HE
    JOHNSON, D
    WONG, SS
    FUKUDA, MN
    [J]. EMBO JOURNAL, 1990, 9 (10) : 3171 - 3178
  • [5] AROSOND NN, 1974, METHOD ENZYMOL, V21, P90
  • [6] MONOCLONAL-ANTIBODIES TO SOLUBLE, HUMAN-MILK GLACTOSYLTRANSFERASE (LACTOSE SYNTHASE-A PROTEIN)
    BERGER, EG
    AEGERTER, E
    MANDEL, T
    HAURI, HP
    [J]. CARBOHYDRATE RESEARCH, 1986, 149 (01) : 23 - 33
  • [7] BIRKY CW, 1983, INT REV CYTOL, P49
  • [8] Golgi dispersal during microtubule disruption: Regeneration of Golgi stacks at peripheral endoplasmic reticulum exit sites
    Cole, NB
    Sciaky, N
    Marotta, A
    Song, J
    LippincottSchwartz, J
    [J]. MOLECULAR BIOLOGY OF THE CELL, 1996, 7 (04) : 631 - 650
  • [9] COLLINS RN, 1992, J BIOL CHEM, V267, P24906
  • [10] STRUCTURAL ASPECTS OF MEMBRANE OF ENDOPLASMIC-RETICULUM
    DEPIERRE, JW
    DALLNER, G
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA, 1975, 415 (04) : 411 - 472