Cell Cycle-Dependent Dynamics of the Golgi-Centrosome Association in Motile Cells.


Journal

Cells
ISSN: 2073-4409
Titre abrégé: Cells
Pays: Switzerland
ID NLM: 101600052

Informations de publication

Date de publication:
25 04 2020
Historique:
received: 25 03 2020
revised: 18 04 2020
accepted: 22 04 2020
entrez: 30 4 2020
pubmed: 30 4 2020
medline: 17 3 2021
Statut: epublish

Résumé

Here, we characterize spatial distribution of the Golgi complex in human cells. In contrast to the prevailing view that the Golgi compactly surrounds the centrosome throughout interphase, we observe characteristic differences in the morphology of Golgi ribbons and their association with the centrosome during various periods of the cell cycle. The compact Golgi complex is typical in G1; during S-phase, Golgi ribbons lose their association with the centrosome and extend along the nuclear envelope to largely encircle the nucleus in G2. Interestingly, pre-mitotic separation of duplicated centrosomes always occurs after dissociation from the Golgi. Shortly before the nuclear envelope breakdown, scattered Golgi ribbons reassociate with the separated centrosomes restoring two compact Golgi complexes. Transitions between the compact and distributed Golgi morphologies are microtubule-dependent. However, they occur even in the absence of centrosomes, which implies that Golgi reorganization is not driven by the centrosomal microtubule asters. Cells with different Golgi morphology exhibit distinct differences in the directional persistence and velocity of migration. These data suggest that changes in the radial distribution of the Golgi around the nucleus define the extent of cell polarization and regulate cell motility in a cell cycle-dependent manner.

Identifiants

pubmed: 32344866
pii: cells9051069
doi: 10.3390/cells9051069
pmc: PMC7290758
pii:
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : NIGMS NIH HHS
ID : R35 GM127098
Pays : United States
Organisme : NIH HHS
ID : S10 OD012324
Pays : United States
Organisme : NIDDK NIH HHS
ID : R01 DK106228
Pays : United States
Organisme : NIGMS NIH HHS
ID : R35 GM130298
Pays : United States
Organisme : NIGMS NIH HHS
ID : R25 GM062459
Pays : United States
Organisme : NIH HHS
ID : S10 OD018075
Pays : United States

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Auteurs

Keyada Frye (K)

Department of Cell and Developmental Biology, Vanderbilt University, Nashville, TN 37240, USA.

Fioranna Renda (F)

Wadsworth Center, New York State Department of Health, Albany, NY 12208, USA.

Maria Fomicheva (M)

Department of Cell and Developmental Biology, Vanderbilt University, Nashville, TN 37240, USA.

Xiaodong Zhu (X)

Department of Cell and Developmental Biology, Vanderbilt University, Nashville, TN 37240, USA.

Lisa Gong (L)

Department of Cell and Developmental Biology, Vanderbilt University, Nashville, TN 37240, USA.

Alexey Khodjakov (A)

Wadsworth Center, New York State Department of Health, Albany, NY 12208, USA.

Irina Kaverina (I)

Department of Cell and Developmental Biology, Vanderbilt University, Nashville, TN 37240, USA.

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Classifications MeSH