ALBERT

Description: Important processes of living cells, including intracellular transport, cell crawling, contraction, division, and mechanochemical signal transduction, are controlled by cytoskeletal (CSK) dynamics. CSK dynamics can be measured by tracking the motion of CSK-bound particles. Particle motion has been reported to follow a superdiffusive behavior that is believed to arise from ATP-driven intracellular stress fluctuations generated by polymerization processes and motor proteins. The power spectrum of intracellular stress fluctuations has been suggested to decay with 1/2 (Lau et al, Phys Rev Lett 91:198101). Here we report direct measurements of cellular force fluctuations that are transmitted to the extracellular matrix, and compared them with the spontaneous motion of CSK-bound beads. Fibronectin coated fluorescent beads (Ø 1 m) were bound to the CSK of confluent human vascular endothelial cells. Forces transmitted to the extracellular matrix (ECM) were quantified by plating these cells onto a collagen coated elastic polyacrylamide hydrogel, and measuring the gel deformation from the displacement of embedded fluorescent beads (Ø 0.5 m). Bead motion of both CSK-bound and ECM-bound beads were measured with nanometer-resolution and expressed as mean square displacement (MSD). The MSD of both CSK-bound and ECM-bound beads displayed a superdiffusive behavior that was well described by a power law: MSD = a*t^b. Surprisingly, we found an identical power law exponent for both CSK-bound and ECM-bound beads of b = 1.6. This finding suggests that the spontaneous motion of CSK-bound beads is driven by stress fluctuations with a 1/ b+1 power spectrum. This result is consistent with the notion that CSK dynamics and CSK stress fluctuations are closely coupled.

Description: Emperor penguins (Aptenodytes forsteri Gray) are the only vertebrate species that breed during the Antarctic winter. From the beginning of the breeding season in April until fledging of the chicks in January, emperor penguins rely on the stability of sea (fast) ice. The International Union for Conservation of Nature (IUCN) has recently listed the species as ‘near threatened’ because the habitat of emperor penguins may deteriorate significantly over the coming years with the anticipated changes in sea ice conditions due to climate change. Since 2009, four emperor penguin colonies have been observed on ice shelves, as opposed to sea ice, during the breeding season (Fretwell et al. 2014). This striking change in their breeding behaviour was interpreted as an adaptation of emperor penguins to poor sea ice conditions. Here we report that a large part of the emperor penguin colony at Atka Bay (Dronning Maud Land, Antarctica) moved onto the ice shelf during the 2013 breeding season. This colony has been regularly observed since 1981 but has never before been seen breeding, incubating their eggs, brooding or crèching on the ice shelf. Our observations concur with a recent report, which documented that altered breeding behaviour in emperor penguins has occurred almost simultaneously across Antarctica (Fretwell et al. 2014). Interestingly, the sea ice at Atka Bay has been stable for three consecutive seasons and thus cannot have triggered this change in behaviour. Rather, we present evidence of increased snow accumulation that has greatly improved the accessibility of the ice shelves around Atka Bay, and we discuss additional meteorological factors and local topographical conditions that may have contributed to the shift in breeding location from sea ice onto an ice shelf.