| 1. |
- Imai, H., et al.
(författare)
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FLASHING: New high-velocity H2O masers in IRAS 18286−0959
- 2020
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Ingår i: Publication of the Astronomical Society of Japan. - : Oxford University Press (OUP). - 2053-051X .- 0004-6264. ; 72:4
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Tidskriftsartikel (refereegranskat)abstract
- We discovered new high-velocity components of H2O maser emission in one of the “water fountain” sources, IRAS 18286−0959, which has been monitored using the Nobeyama 45 m telescope in the FLASHING (Finest Legacy Acquisitions of SiO- and H2O-maser Ignitions by Nobeyama Generation) project since 2018 December. The maser spectra show new components with extremely high expansion velocities (>200 km s−1 projected in the line of sight), some of which are located symmetrically in the spectrum with respect to the systemic velocity. They were also mapped with KaVA (KVN and VERA Combined Array) in 2019 March. We located some of these maser components closer to the central stellar system than other high-velocity components (50-200 km s−1) that have been confirmed to be associated with the known bipolar outflow. The new components would have flashed in the fast collimated jet at a speed of over 300 km s−1 (soon) after 2011 when they had not been detected. The fastest of the new components seem to indicate rapid deceleration in these spectra; however, our present monitoring is still too sparse to unambiguously confirm it (up to 50 km s−1 yr−1) and too short to reveal their terminal expansion velocity, which will be equal to the expansion velocity that has been observed (vexp ∼ 120 km s−1). Future occurrences of such extreme-velocity components may provide a good opportunity to investigate possible recurrent outflow ignitions. Thus, the sculpture of the parental envelope will be traced by the dense gas that is entrained by the fast jet and exhibits spectacular distributions of the relatively stable maser features.
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| 2. |
- Stroikin, Yuri, et al.
(författare)
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Increased resistance of lipofuscin-loaded prematurely senescent fibroblasts to starvation-induced programmed cell death
- 2007
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Ingår i: Biogerontology (Dordrecht). - : Springer Science and Business Media LLC. - 1389-5729 .- 1573-6768. ; 8:1, s. 43-53
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Tidskriftsartikel (refereegranskat)abstract
- Alterations of cellular structures often found in ageing cells is mainly the result of production of reactive oxygen species and a consequence of aerobic life. Both oxidative stress and decreased degradative capacity of lysosomal system cause accumulation of intralysosomal age-related pigment called lipofuscin. To investigate the influence of lipofuscin on cell function, we compared survival of lipofuscin-loaded and control human fibroblasts following complete starvation induced by exposure to phosphate-buffered saline (PBS). Starving of control fibroblasts resulted in lysosomal alkalinisation, relocation of cathepsin D to the cytosol, caspase-3 activation and, finally, cell death, which became evident 72 h after the start of exposure to PBS. Increase of lysosomal pH was significantly less prominent in lipofuscin-loaded cells than in controls and was accompanied neither by leakage of cathepsin D nor by caspase-3 activation even 96 h after the initiation of starvation. Suppression of autophagy by 3-methyladenine (3-MA) accelerated cell death, while inhibition of cathepsin D delayed it, implying an important role of autophagy in cell survival during starvation and showing the involvement of lysosomes in starvation-induced cell death. Disturbed apoptotic response found in lipofuscin-loaded cells can be interpreted as an example of hormesis—an adaptation to low doses of otherwise harmful agents, in this case of lipofuscin, which has a protective effect at moderate amounts but becomes toxic at large quantities.
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| 3. |
- Stroikin, Yuri, et al.
(författare)
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Lysosome-targeted stress reveals increased stability of lipofuscin-containing lysosomes
- 2008
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Ingår i: Age (Omaha). - : Springer. - 0161-9152 .- 1574-4647. ; 30:1, s. 31-42
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Tidskriftsartikel (refereegranskat)abstract
- Cellular ageing is associated with accumulation of undegradable intralysosomal material, called lipofuscin. In order to accelerate the lipofuscin-accumulation, confluent, growth arrested human fibroblasts were cultured under hyperoxic conditions. To provide a better insight into the effects of lipofuscin on cellular functions, we compared lysosomal stability in control and lipofuscin-loaded human fibroblasts under conditions of lysosome-targeted stress induced by exposure to either the lysosomotropic detergent MSDH or the redox-cycling quinone naphthazarin. We show that lysosomal damage, assessed by acridine-orange relocation, translocation of cathepsin D to the cytosol, and alkalinization of lysosomes is more pronounced in control than in lipofuscin-loaded fibroblasts. Finding that lysosomal integrity was less affected or even preserved in case of lipofuscin-loaded cells enables us to suggest that lipofuscin exerts lysosome-stabilizing properties.
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