Lysosome exocytosis is required for mitosis in mammalian cells

被引:4
作者
Nugues, Charlotte [1 ]
Rajamanoharan, Dayani [1 ,3 ]
Burgoyne, Robert D. [1 ]
Haynes, Lee P. [1 ]
Helassa, Nordine [2 ]
机构
[1] Univ Liverpool, Inst Syst Mol & Integrat Biol, Dept Mol Physiol & Cell Signalling, Liverpool L69 3BX, England
[2] Univ Liverpool, Inst Life Course & Med Sci, Fac Hlth & Life Sci, Dept Cardiovasc & Metab Med, Nuffield Bldg,Crown St, Liverpool L69 3BX, England
[3] Unilever PLC, Unilever Res & Dev, Wirral CH62 4ZD, Merseyside, England
基金
英国惠康基金;
关键词
Exocytosis; Lysosome; Mitosis; Phosphoinositide; TIRFM; ACID SPHINGOMYELINASE; MEMBRANE; ACIDIFICATION; VESICLES;
D O I
10.1016/j.bbrc.2022.08.024
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Mitosis, the accurate segregation of duplicated genetic material into what will become two new daughter cells, is accompanied by extensive membrane remodelling and membrane trafficking activities. Early in mitosis, adherent cells partially detach from the substratum, round up and their surface area decreases. This likely results from an endocytic uptake of plasma membrane material. As cells enter cytokinesis they re-adhere, flatten and exhibit an associated increase in surface area. The identity of the membrane donor for this phase of mitosis remains unclear. In this paper we demonstrate how lysosomes dynamically redistribute during mitosis and exocytose. Antagonism of lysosomal exocytosis by pharmacological and genetic approaches causes mitosis failure in a significant proportion of cells. We speculate that either lysosomal membrane or luminal content release, possibly both, are therefore required for normal mitosis progression. These findings are important as they reveal a new process required for successful cell division.(c) 2022 The Authors. Published by Elsevier Inc. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
引用
收藏
页码:211 / 219
页数:9
相关论文
共 33 条
[1]   GPN does not release lysosomal Ca2+ but evokes Ca2+ release from the ER by increasing the cytosolic pH independently of cathepsin C [J].
Atakpa, Peace ;
van Marrewijk, Laura M. ;
Apta-Smith, Michael ;
Chakraborty, Sumita ;
Taylor, Colin W. .
JOURNAL OF CELL SCIENCE, 2019, 132 (03)
[2]   USE OF GLYCYL-L-PHENYLALANINE 2-NAPHTHYLAMIDE, A LYSOSOME-DISRUPTING CATHEPSIN-C SUBSTRATE, TO DISTINGUISH BETWEEN LYSOSOMES AND PRELYSOSOMAL ENDOCYTIC VACUOLES [J].
BERG, TO ;
STROMHAUG, PE ;
LOVDAL, T ;
SEGLEN, PO ;
BERG, T .
BIOCHEMICAL JOURNAL, 1994, 300 :229-236
[3]   PURIFICATION OF AN N-ETHYLMALEIMIDE-SENSITIVE PROTEIN CATALYZING VESICULAR TRANSPORT [J].
BLOCK, MR ;
GLICK, BS ;
WILCOX, CA ;
WIELAND, FT ;
ROTHMAN, JE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (21) :7852-7856
[4]   Endosomal recycling controls plasma membrane area during mitosis [J].
Boucrot, Emmanuel ;
Kirchhausen, Tomas .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2007, 104 (19) :7939-7944
[5]   Plasma Membrane Repair Is Regulated Extracellularly by Proteases Released from Lysosomes [J].
Castro-Gomes, Thiago ;
Corrotte, Matthias ;
Tam, Christina ;
Andrews, Norma W. .
PLOS ONE, 2016, 11 (03)
[6]   Targeting Mitosis in Cancer: Emerging Strategies [J].
Dominguez-Brauer, Carmen ;
Thu, Kelsie L. ;
Mason, Jacqueline M. ;
Blaser, Heiko ;
Bray, Mark R. ;
Mak, Tak W. .
MOLECULAR CELL, 2015, 60 (04) :524-536
[7]   MICROVILLI AND BLEBS AS SOURCES OF RESERVE SURFACE-MEMBRANE DURING CELL SPREADING [J].
ERICKSON, CA ;
TRINKAUS, JP .
EXPERIMENTAL CELL RESEARCH, 1976, 99 (02) :375-384
[8]   Both daughter cells traffic and exocytose membrane at the cleavage furrow during mammalian cytokinesis [J].
Goss, John W. ;
Toomre, Derek K. .
JOURNAL OF CELL BIOLOGY, 2008, 181 (07) :1047-1054
[9]   Interaction of neuronal calcium sensor-1 and ADP-ribosylation factor 1 allows bidirectional control of phosphatidylinositol 4-kinase β and trans-Golgi network-plasma membrane traffic [J].
Haynes, LP ;
Thomas, GMH ;
Burgoyne, RD .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (07) :6047-6054
[10]   Endo-Lysosomal Vesicles Positive for Rab7 and LAMP1 Are Terminal Vesicles for the Transport of Dextran [J].
Humphries, William H. ;
Szymanski, Craig J. ;
Payne, Christine K. .
PLOS ONE, 2011, 6 (10)