A new strategy to improve the CO 2 capture performance of solid amine sorbents has been developed based on the balance of CO 2 kinetic diffusion and thermodynamic sorption. The CO 2 -neutral surfactant was introduced into polyethyleneimine (PEI) to create extra CO 2 transfer pathways, facilitating CO 2 diffusion into the deeper PEI films. Consequently, the sorbents offered increased amount of reactive sites and higher utilization efficiency of amine groups, leading to a dramatically enhanced CO 2 dynamic capacity and total capacity. Due to the facilitating diffusion, the sorbents could work at room temperature with very good performance. At 30 C the surfactant-promoted sorbents had the CO 2 capture capacity as high as 142 mg g À1 and their amine utilization was over 50%, which are the highest values ever reported for the PEI loaded sorbents working at this temperature. The surfactant-promoted sorbents also exhibited much better sorption kinetics and regeneration performance. In addition to advancing the support or amine, the present study provides another costefficient and general approach to design high performance CO 2 solid sorbents and may have a major impact on the advance of current carbon capture and storage technologies.
Cellular senescence, a persistent state of cell cycle arrest, accumulates in aged organisms, contributes to tissue dysfunction, and drives age-related phenotypes. The clearance of senescent cells is expected to decrease chronic, low-grade inflammation and improve tissue repair capacity, thus attenuating the decline of physical function in aged organisms. However, selective and effective clearance of senescent cells of different cell types has proven challenging. Herein, we developed a prodrug strategy to design a new compound based on the increased activity of lysosomal β-galactosidase (β-gal), a primary characteristic of senescent cells. Our prodrug SSK1 is specifically activated by β-gal and eliminates mouse and human senescent cells independently of senescence inducers and cell types. In aged mice, our compound effectively cleared senescent cells in different tissues, decreased the senescence-and age-associated gene signatures, attenuated low-grade local and systemic inflammation, and restored physical function. Our results demonstrate that lysosomal β-gal can be effectively leveraged to selectively eliminate senescent cells, providing a novel strategy to develop anti-aging interventions.Cell Research (2020) 0:1-16; https://doi.
Although major advances in genomics have initiated an exciting new era of research, a lack of information regarding cis-regulatory elements has limited the genetic improvement or manipulation of pigs as a meat source and biomedical model. Here, we systematically characterize cis-regulatory elements and their functions in 12 diverse tissues from four pig breeds by adopting similar strategies as the ENCODE and Roadmap Epigenomics projects, which include RNA-seq, ATAC-seq, and ChIP-seq. In total, we generate 199 datasets and identify more than 220,000 cis-regulatory elements in the pig genome. Surprisingly, we find higher conservation of cis-regulatory elements between human and pig genomes than those between human and mouse genomes. Furthermore, the differences of topologically associating domains between the pig and human genomes are associated with morphological evolution of the head and face. Beyond generating a major new benchmark resource for pig epigenetics, our study provides basic comparative epigenetic data relevant to using pigs as models in human biomedical research.
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