Mitotic Golgi is in a dynamic equilibrium between clustered and free vesicles independent of the ER

被引:49
作者
Jesch, SA
Mehta, AJ
Velliste, M
Murphy, RF
Linstedt, AD
机构
[1] Carnegie Mellon Univ, Dept Biol Sci, Pittsburgh, PA 15213 USA
[2] Carnegie Mellon Univ, Program Biomed & Hlth Engn, Pittsburgh, PA 15213 USA
关键词
ER; Golgi; mitosis; partitioning; vesicles;
D O I
10.1034/j.1600-0854.2001.21203.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Golgi inheritance during cell division involves Golgi disassembly but it remains unclear whether the breakdown product is dispersed vesicles, clusters of vesicles or a fused ER/Golgi network. Evidence against the fused ER/Golgi hypothesis was previously obtained from subcellular fractionation studies, but left concerns about the means used to obtain and disrupt mitotic cells. Here, we performed velocity gradient analysis on otherwise untreated cells shaken from plates 9 h after release from an S-phase block. In addition, we used digitonin and freeze/thaw permeabilization as alternatives to mechanical homogenization. Under each of these conditions, approximately 75% of the Golgi was recovered in a population of small vesicles that lacked detectable ER. We also used multilabel fluorescent microscopy with optical sectioning by deconvolution to compare the 3D metaphase staining pattern of endogenous Golgi and ER markers. Although both ER and Golgi staining were primarily diffuse, only the ER was excluded from the mitotic spindle region. Surprisingly, only 2% of the Golgi fluorescence was present as resolvable structures previously characterized as vesicle clusters. These were not present in the ER pattern. Significantly, a portion of the diffuse Golgi fluorescence, presumably representing dispersed 60-nm vesicles, underwent an apparent rapid aggregation with the larger Golgi structures upon treatments that impaired microtubule integrity. Therefore, mitotic Golgi appears to be in a dynamic equilibrium between clustered and free vesicles, and accurate partitioning may be facilitated by microtubule-based motors acting on the clusters to insure random and uniform distribution of the vesicles.
引用
收藏
页码:873 / 884
页数:12
相关论文
共 45 条
[1]   Signaling via mitogen-activated protein kinase kinase (MEK1) is required for Golgi fragmentation during mitosis [J].
Acharya, U ;
Mallabiabarrena, A ;
Acharya, JK ;
Malhotra, V .
CELL, 1998, 92 (02) :183-192
[2]   The role of microtubule-based motor proteins in maintaining the structure and function of the Golgi complex [J].
Burkhardt, JK .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH, 1998, 1404 (1-2) :113-126
[3]   A specific activation of the mitogen-activated protein kinase kinase 1 (MEK1) is required for Golgi fragmentation during mitosis [J].
Colanzi, A ;
Deerinck, TJ ;
Ellisman, MH ;
Malhotra, V .
JOURNAL OF CELL BIOLOGY, 2000, 149 (02) :331-339
[4]   Golgi dispersal during microtubule disruption: Regeneration of Golgi stacks at peripheral endoplasmic reticulum exit sites [J].
Cole, NB ;
Sciaky, N ;
Marotta, A ;
Song, J ;
LippincottSchwartz, J .
MOLECULAR BIOLOGY OF THE CELL, 1996, 7 (04) :631-650
[5]   Retrograde transport of Golgi-localized proteins to the ER [J].
Cole, NB ;
Ellenberg, J ;
Song, J ;
DiEuliis, D ;
Lippincott-Schwartz, J .
JOURNAL OF CELL BIOLOGY, 1998, 140 (01) :1-15
[6]   Mitotic phosphorylation of the dynein light intermediate chain is mediated by cdc2 kinase [J].
Dell, KR ;
Turck, CW ;
Vale, RD .
TRAFFIC, 2000, 1 (01) :38-44
[7]   Sorting and signaling at the Golgi complex [J].
Donaldson, JG ;
Lippincott-Schwartz, J .
CELL, 2000, 101 (07) :693-696
[8]   Phospholipase A2 antagonists inhibit nocodazole-induced Golgi ministack formation:: Evidence of an ER intermediate and constitutive cycling [J].
Drecktrah, D ;
Brown, WJ .
MOLECULAR BIOLOGY OF THE CELL, 1999, 10 (12) :4021-4032
[9]  
EILENBERG H, 1989, J LIPID RES, V30, P1127
[10]  
Farmaki T, 1999, J CELL SCI, V112, P589