Understanding the mechanism of cell migration and interaction with the microenvironment is not only of critical significance to the function and biology of cells, but also has extreme relevance and impact on physiological processes and diseases such as morphogenesis, wound healing, neuron guidance, and cancer metastasis.

The recent oil spill in the Gulf of Mexico has already caused, and is continuing to cause, significant global environmental issues and has severely impacted people's lives and natural resources. The ramifications of oil spill accidents highlight the difficulty of achieving effective oil–water separation, and the consequences of these accidents are harsh and long-term. In this work, we describe a convenient approach to fabricate cotton textiles with a hydrophilic coating, showing both superhydrophobic and superoleophilic properties. The surfaces are successfully prepared by one-step growth of a diamond-like carbon film onto the textiles via plasma-enhanced chemical vapour deposition and exhibit highly controllable, energy-efficient oil–water separation with high separation efficiency. The results have important implications for oil-absorption dynamics while repelling water completely. The present work suggests encouraging applications to marine spilt oil cleanup and other water–oil separation systems.

Microglial cells participate in brain development and influence neuronal loss and synaptic maturation. Fractalkine is an important neuronal chemokine whose expression increases during development and that can influence microglia function via the fractalkine receptor, CX3CR1. Mice lacking Cx3cr1 show a variety of neuronal defects thought to be the result of deficient microglia function. Activation of CX3CR1 is important for the proper migration of microglia to sites of injury and into the brain during development. However, little is known about how fractalkine modulates microglial properties during development. Here we examined microglial morphology, response to ATP, and K+ current properties in acute brain slices from Cx3cr1 knockout mice across postnatal hippocampal development. We found that fractalkine signaling is necessary for the development of several morphological and physiological features of microglia. Specifically, we found that the occurrence of an outward rectifying K+ current, typical of activated microglia, that peaked during the second and third postnatal week, was reduced in Cx3cr1 knockout mice. Fractalkine signaling also influenced microglial morphology and ability to extend processes in response to ATP following its focal application to the slice. Our results reveal the developmental profile of several morphological and physiological properties of microglia and demonstrate that these processes are modulated by fractalkine signaling.