Light-sheet microscopy reveals dorsoventral asymmetric membrane dynamics of Amoeba proteus during pressure-driven locomotion

被引:4
|
作者
Taniguchi, Atsushi [1 ,2 ,3 ]
Nishigami, Yukinori [3 ]
Kajiura-Kobayashi, Hiroko [4 ]
Takao, Daisuke [5 ,8 ]
Tamaoki, Daisuke [6 ]
Nakagaki, Toshiyuki [3 ]
Nonaka, Shigenori [1 ,2 ]
Sonobe, Seiji [7 ]
机构
[1] Natl Inst Basic Biol, Lab Spatiotemporal Regulat, Okazaki, Aichi, Japan
[2] Exploratory Res Ctr Life & Living Syst ExCELLS, Spatiotemporal Regulat Grp 4448585, Okazaki, Aichi 4448585, Japan
[3] Hokkaido Univ, Res Inst Elect Sci, Sapporo 0010020, Japan
[4] Natl Inst Basic Biol, Lab Regenerat Biol, Okazaki, Aichi 4448585, Japan
[5] Univ Tokyo, Grad Sch Med, Tokyo 1130033, Japan
[6] Univ Toyama, Fac Sci, Acad Assembly, Gofuku, Toyama 9308555, Japan
[7] Univ Hyogo, Grad Sch Life Sci, Kamigori, Hyogo 6781297, Japan
[8] Huazhong Agr Univ, Hubei Hongshan Lab, Key Lab Agr Anim Genet Breeding & Reprod, Minist Educ, Wuhan 430070, Hubei, Peoples R China
来源
BIOLOGY OPEN | 2023年 / 12卷 / 02期
基金
日本学术振兴会;
关键词
Amoeboid locomotion; Cell locomotion; Light sheet microscopy; Membrane dynamics; CELL MOTILITY; NAKED AMEBAS; MIGRATION; MECHANISMS; MOVEMENT; PROTOZOA; SURFACE; FLOW;
D O I
10.1242/bio.059671
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Amoebae are found all around the world and play an essential role in the carbon cycle in the environment. Therefore, the behavior of amoebae is a crucial factor when considering the global environment. Amoebae change their distribution through amoeboid locomotion, which are classified into several modes. In the pressure-driven mode, intracellular hydrostatic pressure generated by the contraction of cellular cortex actomyosin causes the pseudopod to extend. During amoeboid locomotion, the cellular surface exhibits dynamic deformation. Therefore, to understand the mechanism of amoeboid locomotion, it is important to characterize cellular membrane dynamics. Here, to clarify membrane dynamics during pressure-driven amoeboid locomotion, we developed a polkadot membrane staining method and performed light-sheet microscopy in Amoeba proteus, which exhibits typical pressure-driven amoeboid locomotion. It was observed that the whole cell membrane moved in the direction of movement, and the dorsal cell membrane in the posterior part of the cell moved more slowly than the other membrane. In addition, membrane complexity varied depending on the focused characteristic size of the membrane structure, and in general, the dorsal side was more complex than the ventral side. In summary, the membrane dynamics of Amoeba proteus during pressure-driven locomotion are asymmetric between the dorsal and ventral sides.
引用
收藏
页数:8
相关论文
共 7 条
  • [1] Membrane dynamics of dividing cells imaged by lattice light-sheet microscopy
    Aguet, Francois
    Upadhyayula, Srigokul
    Gaudin, Raphael
    Chou, Yi-ying
    Cocucci, Emanuele
    He, Kangmin
    Chen, Bi-Chang
    Mosaliganti, Kishore
    Pasham, Mithun
    Skillern, Wesley
    Legant, Wesley R.
    Liu, Tsung-Li
    Findlay, Greg
    Marino, Eric
    Danuser, Gaudenz
    Megason, Sean
    Betzig, Eric
    Kirchhausen, Tom
    MOLECULAR BIOLOGY OF THE CELL, 2016, 27 (22) : 3418 - 3435
  • [2] High-speed panoramic light-sheet microscopy reveals global endodermal cell dynamics
    Benjamin Schmid
    Gopi Shah
    Nico Scherf
    Michael Weber
    Konstantin Thierbach
    Citlali Pérez Campos
    Ingo Roeder
    Pia Aanstad
    Jan Huisken
    Nature Communications, 4
  • [3] High-speed panoramic light-sheet microscopy reveals global endodermal cell dynamics
    Schmid, Benjamin
    Shah, Gopi
    Scherf, Nico
    Weber, Michael
    Thierbach, Konstantin
    Campos, Citlali Perez
    Roeder, Ingo
    Aanstad, Pia
    Huisken, Jan
    NATURE COMMUNICATIONS, 2013, 4
  • [4] Imaging Proteins, Cells, and Tissues Dynamics during Embryogenesis with Two-Photon Light-Sheet Microscopy
    Truong, Thai V.
    Holland, Daniel B.
    Trivedi, Vikas
    Fraser, Scott E.
    BIOPHYSICAL JOURNAL, 2013, 104 (02) : 337A - 337A
  • [5] Lattice Light-Sheet Microscopy of Dividing Cells in Culture and in Live Zebrafish Embryos With High Spatiotemporal Resolution Demonstrates Similar Membrane and Cell Volume Dynamics.
    Upadhyayula, S.
    Aguet, F.
    Gaudin, R.
    Coccuci, E.
    He, K.
    Chen, B.
    Mosaliganti, K. R.
    Legant, W. R.
    Liu, T.
    Marino, E.
    Danuser, G.
    Megason, S. G.
    Betzig, E.
    Kirchhausen, T.
    MOLECULAR BIOLOGY OF THE CELL, 2015, 26
  • [6] 5D imaging via light sheet microscopy reveals cell dynamics during the eye-antenna disc primordium formation in Drosophila
    Huang, Yu Shan
    Ku, Hui Yu
    Tsai, Yun Chi
    Chang, Chin Hao
    Pao, Sih Hua
    Sun, Y. Henry
    Chiou, Arthur
    SCIENTIFIC REPORTS, 2017, 7
  • [7] 5D imaging via light sheet microscopy reveals cell dynamics during the eye-antenna disc primordium formation in Drosophila
    Yu Shan Huang
    Hui Yu Ku
    Yun Chi Tsai
    Chin Hao Chang
    Sih Hua Pao
    Y. Henry Sun
    Arthur Chiou
    Scientific Reports, 7