Search Results (2)

Liquid-crystal columns were prepared and observed under microgravity aboard suborbital TEXUS rocket flights. The microgravity phase of each flight lasted for approximately six minutes. We tested structures in different liquid-crystalline mesophases. In the isotropic and nematic phases, the Rayleigh-Plateau instability led to the collapse of the columns. However, in the smectic A and C mesophases, it was found that the columns survived the extension to slenderness ratios (length/diameter) of over 4.5 (and in one case, more than 6). The liquid-crystalline material in the millimeter-sized columns was macroscopically disordered. Thus, regular shell-like internal layer structures that stabilized the columns can be excluded. Instead, the reason for their persistence was the yield stress of the material, which is quite different for the different mesophases. In the columnar mesophase, the cylindrical bridge even survived the strong deceleration when the rocket re-entered the atmosphere. During the breakup of the filaments, the neck thinning dynamics were determined. Full article

The FLUMIAS (Fluorescence-Microscopic Analyses System for Life-Cell-Imaging in Space) confocal laser spinning disk fluorescence microscope represents a new imaging capability for live cell imaging experiments on suborbital ballistic rocket missions. During the second pioneer mission of this microscope system on the TEXUS-54 suborbital rocket flight, we developed and performed a live imaging experiment with primary human macrophages. We simultaneously imaged four different cellular structures (nucleus, cytoplasm, lysosomes, actin cytoskeleton) by using four different live cell dyes (Nuclear Violet, Calcein, LysoBrite, SiR-actin) and laser wavelengths (405, 488, 561, and 642 nm), and investigated the cellular morphology in microgravity (10⁻⁴ to 10⁻⁵ g) over a period of about six minutes compared to 1 g controls. For live imaging of the cytoskeleton during spaceflight, we combined confocal laser microscopy with the SiR-actin probe, a fluorogenic silicon-rhodamine (SiR) conjugated jasplakinolide probe that binds to F-actin and displays minimal toxicity. We determined changes in 3D cell volume and surface, nuclear volume and in the actin cytoskeleton, which responded rapidly to the microgravity environment with a significant reduction of SiR-actin fluorescence after 4–19 s microgravity, and adapted subsequently until 126–151 s microgravity. We conclude that microgravity induces geometric cellular changes and rapid response and adaptation of the potential gravity-transducing cytoskeleton in primary human macrophages. Full article