Disruption of microtubules inhibits cytoplasmic ribonucleoprotein stress granule formation

被引:117
|
作者
Ivanov, PA
Chudinova, EM
Nadezhdina, ES [1 ]
机构
[1] Russian Acad Sci, Inst Prot Res, Pushchino 142292, Moscow Region, Russia
[2] Moscow MV Lomonosov State Univ, AN Belozersky Inst Physicochem Biol, Moscow 119899, Russia
关键词
translation initiation factor-3; eIF3a; PABP; stress granules; arsenate; microtubule; actin; nocodazole; paclitaxel; latrunculin B;
D O I
10.1016/S0014-4827(03)00290-8
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Stress granules are RNP-containing particles arising in the cytoplasm in response to environmental stress. They are dynamic structures assembling and disassembling in the cytoplasm very rapidly. We have studied whether the cytoskeleton is involved in the formation of stress granules. Stress granules were induced in CV-1 cells by sodium arsenate treatment and visualized by immunofluorescent staining with antibodies either to the p170 subunit of eIF3 or to poly(A)-binding protein. Treatment with sodium arsenate for 30-120 min led to assembling of stress granules in a majority of CV-1 cells. Disruption of MT array with nocodazole treatment abolished arsenate-induced formation of stress granules. A similar effect was induced by the microtubule-depolymerizing drug vinblastine, though the influence of the microtubule-stabilizing drug paclitaxel was opposite. Nocodazole treatment did not prevent arsenate-induced phosphorylation of the eIF-2alpha factor, essential for stress granule formation, suggesting that the presence of intact MT array is required for granule assembly. Unexpectedly, treatment of cells with the actin filament-disrupting drug latrunculin B slightly enhanced stress granule formation. We propose that stress granule formation is microtubule-dependent process and likely is facilitated by the motor protein-driven movement of individual stress granule components (e.g., mRNP) along microtubules. (C) 2003 Elsevier Inc. All rights reserved.
引用
收藏
页码:227 / 233
页数:7
相关论文
共 50 条
  • [31] Cytoplasmic localization of amyotrophic lateral sclerosis-related TDP-43 proteins modulates stress granule formation
    Besnard-Guerin, Corinne
    EUROPEAN JOURNAL OF NEUROSCIENCE, 2020, 52 (08) : 3995 - 4008
  • [32] ELUCIDATING THE ROLE OF STRESS GRANULE FORMATION IN MEDULLOBLASTOMA
    Langman, Sofya
    Lizardo, Michael
    Forget, Antoine
    Ayrault, Olivier
    Sorensen, Poul
    NEURO-ONCOLOGY, 2019, 21 : 112 - 112
  • [33] Regulation of stress granule formation in human oligodendrocytes
    Florian Pernin
    Qiao-Ling Cui
    Abdulshakour Mohammadnia
    Milton G. F. Fernandes
    Jeffery A. Hall
    Myriam Srour
    Roy W. R. Dudley
    Stephanie E. J. Zandee
    Wendy Klement
    Alexandre Prat
    Hannah E. Salapa
    Michael C. Levin
    G. R. Wayne Moore
    Timothy E. Kennedy
    Christine Vande Velde
    Jack P. Antel
    Nature Communications, 15
  • [34] Regulation of stress granule formation in human oligodendrocytes
    Pernin, Florian
    Cui, Qiao-Ling
    Mohammadnia, Abdulshakour
    Fernandes, Milton G. F.
    Hall, Jeffery A.
    Srour, Myriam
    Dudley, Royw. R.
    Zandee, Stephanie E. J.
    Klement, Wendy
    Prat, Alexandre
    Salapa, Hannah E.
    Levin, Michael C.
    Moore, G. R. Wayne
    Kennedy, Timothy E.
    Vande Velde, Christine
    Antel, Jack P.
    NATURE COMMUNICATIONS, 2024, 15 (01)
  • [35] Stress granule formation helps to mitigate neurodegeneration
    Glineburg, M. Rebecca
    Yildirim, Evrim
    Gomez, Nicolas
    Rodriguez, Genesis
    Pak, Jaclyn
    Li, Xingli
    Altheim, Christopher
    Waksmacki, Jacob
    McInerney, Gerald M.
    Barmada, Sami J.
    Todd, Peter K.
    NUCLEIC ACIDS RESEARCH, 2024, 52 (16) : 9745 - 9759
  • [36] Impact of protein domains on the MEL2 granule, a cytoplasmic ribonucleoprotein complex maintaining faithful meiosis progression in rice
    Mimura, Manaki
    Ono, Seijiro
    Somashekar, Harsha
    Nonomura, Ken-Ichi
    NEW PHYTOLOGIST, 2024, 243 (06) : 2235 - 2250
  • [37] Shigella flexneri modulates stress granule composition and inhibits stress granule aggregation (vol 18, pg 922, 2016)
    Vonaesch, Pascale
    Campbell-Valois, Francois-Xavier
    Dufour, Alexandre
    Sansonetti, Philippe J.
    Schnupf, Pamela
    CELLULAR MICROBIOLOGY, 2016, 18 (12) : 1892 - 1892
  • [38] TM4SF1-AS1 inhibits apoptosis by promoting stress granule formation in cancer cells
    Kitajima, Hiroshi
    Maruyama, Reo
    Niinuma, Takeshi
    Yamamoto, Eiichiro
    Takasawa, Akira
    Takasawa, Kumi
    Ishiguro, Kazuya
    Tsuyada, Akihiro
    Suzuki, Ryo
    Sudo, Gota
    Kubo, Toshiyuki
    Mitsuhashi, Kei
    Idogawa, Masashi
    Tange, Shoichiro
    Toyota, Mutsumi
    Yoshido, Ayano
    Kumegawa, Kohei
    Kai, Masahiro
    Yanagihara, Kazuyoshi
    Tokino, Takashi
    Osanai, Makoto
    Nakase, Hiroshi
    Suzuki, Hiromu
    CELL DEATH & DISEASE, 2023, 14 (07)
  • [39] TM4SF1-AS1 inhibits apoptosis by promoting stress granule formation in cancer cells
    Hiroshi Kitajima
    Reo Maruyama
    Takeshi Niinuma
    Eiichiro Yamamoto
    Akira Takasawa
    Kumi Takasawa
    Kazuya Ishiguro
    Akihiro Tsuyada
    Ryo Suzuki
    Gota Sudo
    Toshiyuki Kubo
    Kei Mitsuhashi
    Masashi Idogawa
    Shoichiro Tange
    Mutsumi Toyota
    Ayano Yoshido
    Kohei Kumegawa
    Masahiro Kai
    Kazuyoshi Yanagihara
    Takashi Tokino
    Makoto Osanai
    Hiroshi Nakase
    Hiromu Suzuki
    Cell Death & Disease, 14
  • [40] The combined disruption of microfilaments and microtubules affects the distribution and function of GABAA receptors in rat cerebellum granule cells in culture
    Luccardini, C
    Casagrande, S
    Cupello, A
    Pellistri, F
    Ramoino, P
    Robello, M
    NEUROSCIENCE LETTERS, 2004, 359 (1-2) : 25 - 28