Simulated microgravity influences circadian rhythm of NIH3T3 cells

被引:5
|
作者
Yang, Shuhong [1 ]
Liu, Yanyou [1 ]
Yang, Yunyun [1 ]
Yang, Zhenhua [1 ]
Cheng, Shuting [1 ]
Hou, Wang [1 ]
Wang, Yuhui [1 ]
Jiang, Zhou [1 ]
Xiao, Jing [1 ]
Guo, Huiling [1 ]
Wang, Zhengrong [1 ]
机构
[1] Sichuan Univ, Preclin & Forens Med Sch, Hlth Minist Key Lab Chronobiol, Chengdu, Peoples R China
关键词
Simulated microgravity; circadian rhythm; MEK; ERK pathway; zeitgeber; NIH3T3; cells; MAP KINASE CASCADE; GENE-EXPRESSION; CLOCK MECHANISM; TIMING SYSTEM; NEGATIVE LIMB; FIBROBLASTS; TEMPERATURE; FEEDBACK; MECHANOTRANSDUCTION; OSCILLATORS;
D O I
10.1080/09291016.2016.1207391
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Gravity heavily influences living organisms on earth including their circadian rhythm, which is fundamentally important for coordinately physiology in organisms as diverse as cyanobacteria, fungus and humans. Numerous researches have revealed that microgravity in outer space can affect circadian rhythm of astronauts and rodent animals, but the mechanism remains unknown. Using rotary cell culture system to simulate microgravity environment, we investigated the role of simulated microgravity in regulating the circadian rhythm of NIH3T3 cells. Our experiments found that simulated microgravity can not only influence the mRNA level of some core circadian genes, but also modify the circadian rhythm of Per1 and Per2 synchronized after phorbol myristate acetate treatment. Remarkably, MEK/ERK pathway was transiently activated after a 2-h simulated microgravity treatment, with a significant upregulation of Kras, Raf1 and p-ERK1/ERK2. Moreover, U0126, a selective inhibitor of MEK/ERK pathway, could disrupt the circadian rhythm of Per1 and Per2 synchronized after simulated microgravity treatment. Together, our results unveil that simulated microgravity could act like a zeitgeber to influence the circadian rhythm of NIH3T3 by acting on MEK/ERK pathway, indicating that MEK/ERK pathway may act as a bridge which connects cells mechanotransduction pathway and circadian rhythm regulation.
引用
收藏
页码:897 / 907
页数:11
相关论文
共 50 条
  • [31] Rapid senescence induced by overexpression of p53 in NIH3T3 cells
    HU Jiancheng
    Chinese Science Bulletin, 2001, (08) : 653 - 656
  • [32] Malignant transformation of NIH3T3 cells by overexpression of mot-2 protein
    Kaul, SC
    Duncan, EL
    Englezou, A
    Takano, S
    Reddel, RR
    Mitsui, Y
    Wadhwa, R
    ONCOGENE, 1998, 17 (07) : 907 - 911
  • [33] MAP KINASE ACTIVATION IS ESSENTIAL FOR ONCOGENIC TRANSFORMATION OF NIH3T3 CELLS BY MOS
    OKAZAKI, K
    SAGATA, N
    ONCOGENE, 1995, 10 (06) : 1149 - 1157
  • [34] INTERNALIZATION AND RECYCLING OF CD4 TRANSFECTED INTO HELA AND NIH3T3 CELLS
    PELCHENMATTHEWS, A
    ARMES, JE
    MARSH, M
    EMBO JOURNAL, 1989, 8 (12): : 3641 - 3649
  • [35] Rapid senescence induced by overexpression of p53 in NIH3T3 cells
    Hu, JC
    Lei, Y
    Hong, X
    Lu, ZG
    Zhai, ZH
    CHINESE SCIENCE BULLETIN, 2001, 46 (08): : 653 - +
  • [36] Changes of phenotypes associated with activated Src by overexpressed PTPα in NIH3T3 cells
    Yang, JS
    Zheng, XM
    Chen, SS
    ACTA BIOCHIMICA ET BIOPHYSICA SINICA, 2002, 34 (02): : 193 - 198
  • [37] THE MAJOR RAS INDUCED PROTEIN IN NIH3T3 CELLS IS CATHEPSIN-L
    JOSEPH, L
    LAPID, S
    SUKHATME, V
    NUCLEIC ACIDS RESEARCH, 1987, 15 (07) : 3186 - 3186
  • [38] TRANSFORMATION OF NIH3T3 CELLS WITH SYNTHETIC C-HA-RAS GENES
    KAMIYA, H
    MIURA, K
    OHTOMO, N
    KODA, T
    KAKINUMA, M
    NISHIMURA, S
    OHTSUKA, E
    JAPANESE JOURNAL OF CANCER RESEARCH, 1989, 80 (03): : 200 - 203
  • [39] MORPHOLOGICAL REVERSION OF SIS-TRANSFORMED NIH3T3 CELLS BY TRICHOSTATIN-A
    SUGITA, K
    KOIZUMI, K
    YOSHIDA, H
    CANCER RESEARCH, 1992, 52 (01) : 168 - 172
  • [40] Malignant transformation of NIH3T3 cells by overexpression of mot-2 protei
    Sunil C Kaul
    Emma L Duncan
    Anna Englezou
    Syuichi Takano
    Roger R Reddel
    Youji Mitsui
    Renu Wadhwa
    Oncogene, 1998, 17 : 907 - 911