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Biology subjects

Zhang, Y.-R.

Publications and source records attributed to Zhang, Y.-R..

2 recordsLinked to original sources

New insights into tissue-specific responses and interactive characteristics of crop-microbe "One Health" system to soil chromium and ofloxacin pollution

This study firstly investigated the tissue-specific responses and interactive characteristics of the crop-microbe system to co-pollution with ofloxacin (OFL) and chromium (Cr) in soil. The results emphasized the hormesis effect induced by low-dose OFL (1 mg L-1) on ginger plants subjected to soil Cr stress. However, high-dose OFL (100 mg L-1) and Cr co-stressed plants exhibited reduced growth, root activity, antioxidant enzyme activities and photosynthesis-fluorescence performances, while the reactive oxygen species (ROS) reflected by O2{middle dot}- and H2O2 significantly increased up to 43.34% and 78.63%, respectively, compared to other treatments. In addition, high-throughput sequencing indicated that OFL influenced rhizosphere microbial diversity, composition, and evolution, favoring Proteobacteria proliferation under co-pollution. Meanwhile, root exudate patterns shifted, with humic-like exudates, potentially interacting with pollutants and microbes. Notably, enrichments of antibiotic resistance gene (qnrS) in edible rhizome and potential pathogenic bacteria in ginger rhizosphere were observed under OFL and Cr co-pollution, raising environmental and food chain concerns. Through structural equation modeling, we quantitatively established correlations within soil-crop-microbe factors, emphasizing their interconnected nature. Overall, this study sheds light on the complex responses of the crop-microbe system to OFL and Cr co-pollution, highlighting the importance of understanding pollutant interactions for enhancing plant resilience and mitigating environmental risks. HighlightsO_LIRevealed a hormesis from low-dose OFL on Cr-polluted ginger, enhancing resilience. C_LIO_LIRhizosphere microbial composition shift under co-pollution, favoring Proteobacteria. C_LIO_LIqnrS and potential pathogens increased under co-pollution, posing food chain risks. C_LIO_LIStructural equation modeling quantified correlations in soil- crop-microbe factors. C_LIO_LIClarified crop-microbe "One Health" interactions role under Cr & OFL co-pollution. C_LI Graphical abstract O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=128 SRC="FIGDIR/small/561380v1_ufig1.gif" ALT="Figure 1"> View larger version (61K): org.highwire.dtl.DTLVardef@bd3d20org.highwire.dtl.DTLVardef@1f8024eorg.highwire.dtl.DTLVardef@15f6154org.highwire.dtl.DTLVardef@ef0aeb_HPS_FORMAT_FIGEXP M_FIG C_FIG

physiology↗

Lactylation-driven FTO-mediated m6A modification of CDK2 aggravates diabetic microvascular anomalies

Diabetic retinopathy (DR) is a leading cause of irreversible vision loss in working-age populations. FTO is an N6-methyladenosine (m6A) demethylase that participates in various biological events, while its role in DR remains elusive. Herein, we detected elevated FTO expression in retinal proliferative membranes of DR patients. FTO promoted endothelial cell (EC) cell cycle progression and tip cell formation to facilitate angiogenesis in vitro, in mice and in zebrafish. FTO also regulated EC-pericyte crosstalk to trigger diabetic microvascular leakage, and mediated EC-microglia interactions to induce retinal inflammation and neurodegeneration in vivo and in vitro. Mechanistically, FTO affected EC features via modulating CDK2 mRNA stability in an m6A-YTHDF2-dependent manner. FTO up-regulation under diabetic conditions was driven by lactate mediated histone lactylation. FB23-2, an inhibitor to FTOs m6A demethylase activity, suppressed angiogenic phenotypes in vivo and in vitro. Noteworthy, we developed a nanoplatform encapsulating FB23-2 for systemic administration, and confirmed its targeting and therapeutic efficiencies in mice. Collectively, our study demonstrated that FTO coordinates EC biology and retinal homeostasis in DR, providing a promising nanotherapeutic approach for DR.

cell biology↗