Publications by authors named "Shibo Meng"

Aqueous zinc ion batteries (AZIBs), which have attracted attentions in the field of energy storage, is affected by dendrites and side reactions of Zn anode, resulting in an unsatisfactory performance of AZIBs. Herein, we propose a biased adsorption strategy mediated by straight-chain molecule (Scm) for stabilizing Zn anode. The dual polar termini of Scms guaranties securely anchor themselves in a parallel orientation upon the Zn anode surface.

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In response to varying environments along urban and rural gradients, invasive plants may strategically allocate resources to enhance their invasiveness. However, how invasive plants balance their resources for growth, reproduction, and defense as responses to biotic and abiotic factors across these gradients remain unclear. We conducted field surveys on the growth, reproduction, and herbivory of the invasive species Phytolacca americana across diverse urban and rural habitats.

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Background: Extensive hepatocyte mortality and the absence of specific medical therapy significantly contribute to the unfavorable prognosis of acute liver failure (ALF). Ferroptosis is a crucial form of cell death involved in ALF. In this study, we aimed to determine the impact of Mediator complex subunit 1 (Med1) on ferroptosis and its potential hepatoprotective effects in ALF.

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Article Synopsis
  • The study investigates the immune responses involved in hepatitis B surface antigen (HBsAg) loss during pegylated interferon-α (PEG-IFN) therapy, focusing on the type I inflammatory response in patients with chronic hepatitis B (CHB).
  • Out of 82 patients, those who achieved HBsAg loss (cured group) showed higher levels of IFN-γ Th1 cells and had different chemokine levels compared to those who did not achieve HBsAg loss (uncured group), suggesting a link between these immune markers and treatment outcomes.
  • The research indicates that M1 macrophages play a crucial role in HBsAg loss by enhancing the function of memory
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Background: Acute-on-chronic liver failure (ACLF) is a major challenge in the field of hepatology. While mesenchymal stem cell (MSC) therapy can improve the prognosis of patients with ACLF, the molecular mechanisms through which MSCs attenuate ACLF remain poorly understood. We performed global miRNA and mRNA expression profiling via next-generation sequencing of liver tissues from MSC-treated ACLF mice to identify important signaling pathways and major factors implicated in ACLF alleviation by MSCs.

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Acute-on-chronic liver failure (ACLF) is a severe disease with a high mortality. Macrophage-related inflammation plays a crucial role in ACLF development. Mesenchymal stem cells (MSCs) treatment was demonstrated to be beneficial in ACLF in our previous study; however, the underlying mechanisms remain unknown.

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