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Jianhuo Fang

Center for Life Sciences

ORCID: 0000-0001-9742-7673

Publishes on RNA Research and Splicing, RNA modifications and cancer, Cancer-related molecular mechanisms research. 20 papers and 2.7k citations.

20Publications
2.7kTotal Citations

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Top publicationsby citations

Inhalable Microorganisms in Beijing’s PM<sub>2.5</sub> and PM<sub>10</sub> Pollutants during a Severe Smog Event
Chen Cao, Wenjun Jiang, Buying Wang et al.|Environmental Science & Technology|2014
Cited by 685Open Access

Particulate matter (PM) air pollution poses a formidable public health threat to the city of Beijing. Among the various hazards of PM pollutants, microorganisms in PM2.5 and PM10 are thought to be responsible for various allergies and for the spread of respiratory diseases. While the physical and chemical properties of PM pollutants have been extensively studied, much less is known about the inhalable microorganisms. Most existing data on airborne microbial communities using 16S or 18S rRNA gene sequencing to categorize bacteria or fungi into the family or genus levels do not provide information on their allergenic and pathogenic potentials. Here we employed metagenomic methods to analyze the microbial composition of Beijing's PM pollutants during a severe January smog event. We show that with sufficient sequencing depth, airborne microbes including bacteria, archaea, fungi, and dsDNA viruses can be identified at the species level. Our results suggested that the majority of the inhalable microorganisms were soil-associated and nonpathogenic to human. Nevertheless, the sequences of several respiratory microbial allergens and pathogens were identified and their relative abundance appeared to have increased with increased concentrations of PM pollution. Our findings may serve as an important reference for environmental scientists, health workers, and city planners.

Scleral hypoxia is a target for myopia control
Hao Wu, Wei Chen, Fei Zhao et al.|Proceedings of the National Academy of Sciences|2018
Cited by 507Open Access

) promoted myofibroblast transdifferentiation with down-regulation of type I collagen in human scleral fibroblasts. Importantly, the antihypoxia drugs salidroside and formononetin down-regulated HIF-1α expression as well as the phosphorylation levels of eIF2α and mTOR, slowing experimental myopia progression without affecting normal ocular growth in guinea pigs. Furthermore, eIF2α phosphorylation inhibition suppressed experimental myopia, whereas mTOR phosphorylation induced myopia in normal mice. Collectively, these findings defined an essential role of hypoxia in scleral ECM remodeling and myopia development, suggesting a therapeutic approach to control myopia by ameliorating hypoxia.