Light-sheet microscopy reveals dorsoventral asymmetric membrane dynamics ofAmoeba proteusduring pressure-driven locomotion

Author:

Taniguchi Atsushi123,Nishigami Yukinori3ORCID,Kajiura-Kobayashi Hiroko4,Takao Daisuke5,Tamaoki Daisuke6,Nakagaki Toshiyuki3,Nonaka Shigenori12,Sonobe Seiji7

Affiliation:

1. National Institute for Basic Biology 1 Laboratory for Spatiotemporal Regulations , , Okazaki, Aichi , Japan

2. Exploratory Research Center on Life and Living Systems (ExCELLS), Okazaki 2 Spatiotemporal Regulations 444-8585 Group , , Aichi 444-8585 , Japan

3. Research Institute for Electronic Science, Hokkaido University 3 , Sapporo 001-0020 , Japan

4. National Institute for Basic Biology 4 Laboratory of Regeneration Biology , , Okazaki, Aichi 444-8585 , Japan

5. Graduate School of Medicine, The University of Tokyo 5 , Bunkyo, Tokyo 113-0033 , Japan

6. University of Toyama 6 Faculty of Science, Academic Assembly , , Gofuku, Toyama 930-8555 , Japan

7. Graduate School of Life Science, University of Hyogo 7 , Kamigori, Hyogo 678-1297 , Japan

Abstract

ABSTRACTAmoebae 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.This article has an associated interview with the co-first authors of the paper.

Funder

Japan Society for the Promotion of Science

Hokkaido University

Ministry of Education, Culture, Sports, Science and Technology

National Institute for Basic Biology

Publisher

The Company of Biologists

Subject

General Agricultural and Biological Sciences,General Biochemistry, Genetics and Molecular Biology

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