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Effects of the piezo-tolerance of cultured deep-sea eel cells on survival rates, cell proliferation, and cytoskeletal structures

机译:培养的深海鳗鱼细胞耐压电性对存活率,细胞增殖和细胞骨架结构的影响

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摘要

We investigated the pressure tolerance of deep-sea eel (Simenchelys parasiticus; habitat depth, 366-2,630 m) cells, conger eel (Conger myriaster) cells, and mouse 3T3-L1 cells. Although there were no living mouse 3T3-L1 and conger eel cells after 130 MPa (0.1 MPa = 1 bar) hydrostatic pressurization for 20 min, all deep-sea eel cells remained alive after being subjected to pressures up to 150 MPa for 20 min. Pressurization at 40 MPa for 20 min induced disruption of actin and tubulin filaments with profound cell-shape changes in the mouse and conger eel cells. In the deep-sea eel cells, microtubules and some actin filaments were disrupted after being subjected to hydrostatic pressure of 100 MPa and greater for 20 min. Conger eel cells were sensitive to pressure and did not grow at 10 MPa. Mouse 3T3-L1 cells grew faster under pressure of 5 MPa than at atmospheric pressure and stopped growing at 18 MPa. Deep-sea eel cells were capable of growth in pressures up to 25 MPa and stopped growing at 30 MPa. Deep-sea eel cells required 4 h at 20 MPa to finish the M phase, which was approximately fourfold the time required under atmospheric conditions.
机译:我们调查了深海鳗(Simenchelys parasiticus;栖息地深度,366-2,630 m)细胞,海鳗(Conger myriaster)细胞和小鼠3T3-L1细胞的耐压性。尽管在130 MPa(0.1 MPa = 1 bar)静水加压20分钟后没有活着的小鼠3T3-L1和会聚鳗鱼细胞,但所有深海鳗鱼细胞在承受高达150 MPa的压力20分钟后仍然存活。在40 MPa下加压20分钟会诱导肌动蛋白和微管蛋白细丝破裂,并在小鼠和鳗鱼细胞中发生深刻的细胞形状变化。在深海鳗鱼细胞中,微管和一些肌动蛋白丝经受100 MPa以上的静水压力20分钟后破裂。鳗鱼细胞对压力敏感,在10 MPa时不生长。小鼠3T3-L1细胞在5 MPa的压力下比在大气压下生长更快,并在18 MPa时停止生长。深海鳗鱼细胞能够在高达25 MPa的压力下生长,并在30 MPa时停止生长。深海鳗鱼细胞在20 MPa下需要4小时才能完成M相,这大约是大气条件下所需时间的四倍。

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