Safeguarding the rooftop scenery of Old Beijing
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Worldwide rooftop photovoltaic electricity generation may mitigate global warming
Rooftop photovoltaic (RPV) is often understood as a niche contribution to climate change mitigation. However, the global potential of RPVs to mitigate global warming is unknown. Here we map the global rooftop area at 1-km resolution, quantifying 286,393 km2 of rooftops worldwide through geospatial data mining and artificial intelligence techniques. Using nine advanced Earth system models from the coupled model intercomparison project phase 6, we reveal that RPVs could substantially contribute to reducing global temperatures by 0.05–0.13 °C before 2050. Region-specific analysis underscores the variability in RPV potential and the necessity of tailored approaches to optimize RPV deployment, considering local solar resources, existing infrastructure and grid carbon intensity. Our findings reveal that leveraging RPV systems offers a viable and impactful strategy for reducing carbon footprints and combating climate change globally, while advocating targeted interventions to enhance the benefits of RPVs, particularly in areas with high solar radiation or rapid urbanization.
Improved radicchio seedling growth under CsPbI3 perovskite rooftop in a laboratory-scale greenhouse for Agrivoltaics application
Agrivoltaics, integrating photovoltaic systems with crop cultivation, demands semitransparent solar modules to mitigate soil shadowing. Perovskite Solar Cells (PSC) offer competitive efficiency, low fabrication costs, and high solar transmittance, making them suitable for agrivoltaic applications. However, the impact of PSC light filtering on plant growth and transcriptomics remains underexplored. This study investigates the viability and agronomic implications of the growth of radicchio seedlings (Cichorium intybus var. latifolium) in laboratory-scale greenhouses integrating Perovskites-coated rooftops. Eu-enriched CsPbI3 layers are chosen to provide semi-transparency and phase stability while radicchio has limited size and grows in pots. Despite the reduced light exposure, radicchio seedlings exhibit faster growth and larger leaves than in the reference, benefiting from specific spectral filtering. RNA-sequencing reveals differential gene expression patterns reflecting adaptive responses to environmental changes. Simulations of full PSC integration demonstrate a positive energy balance in greenhouses to cover annual energy needs for lighting, irrigation, and air conditioning.
Air, surface, and wastewater surveillance of SARS-CoV-2; a multimodal evaluation of COVID-19 detection in a built environment
Environmental surveillance of infectious organisms holds tremendous promise to reduce human-to-human transmission in indoor spaces through early detection.
Reducing functionally defective old HSCs alleviates aging-related phenotypes in old recipient mice
Aging is a process accompanied by functional decline in tissues and organs with great social and medical consequences. Developing effective anti-aging strategies is of great significance. In this study, we demonstrated that transplantation of young hematopoietic stem cells (HSCs) into old mice can mitigate aging phenotypes, underscoring the crucial role of HSCs in the aging process. Through comprehensive molecular and functional analyses, we identified a subset of HSCs in aged mice that exhibit “younger” molecular profiles and functions, marked by low levels of CD150 expression. Mechanistically, CD150low HSCs from old mice but not their CD150high counterparts can effectively differentiate into downstream lineage cells. Notably, transplantation of old CD150low HSCs attenuates aging phenotypes and prolongs lifespan of elderly mice compared to those transplanted with unselected or CD150high HSCs. Importantly, reducing the dysfunctional CD150high HSCs can alleviate aging phenotypes in old recipient mice. Thus, our study demonstrates the presence of “younger” HSCs in old mice, and that aging-associated functional decline can be mitigated by reducing dysfunctional HSCs.
Exosome-based targeted delivery of NF-κB ameliorates age-related neuroinflammation in the aged mouse brain
Neuroinflammation, a significant contributor to various neurodegenerative diseases, is strongly associated with the aging process; however, to date, no efficacious treatments for neuroinflammation have been developed. In aged mouse brains, the number of infiltrating immune cells increases, and the key transcription factor associated with increased chemokine levels is nuclear factor kappa B (NF-κB). Exosomes are potent therapeutics or drug delivery vehicles for various materials, including proteins and regulatory genes, to target cells. In the present study, we evaluated the therapeutic efficacy of exosomes loaded with a nondegradable form of IκB (Exo-srIκB), which inhibits the nuclear translocation of NF-κB to suppress age-related neuroinflammation. Single-cell RNA sequencing revealed that these anti-inflammatory exosomes targeted macrophages and microglia, reducing the expression of inflammation-related genes. Treatment with Exo-srIκB also suppressed the interactions between macrophages/microglia and T and B cells in the aged brain. We demonstrated that Exo-srIκB successfully alleviates neuroinflammation by primarily targeting activated macrophages and partially modulating the functions of age-related interferon-responsive microglia in the brain. Thus, our findings highlight Exo-srIκB as a potential therapeutic agent for treating age-related neuroinflammation.
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