Publications by authors named "Xinbo Wei"

Article Synopsis
  • Endothelial cell (EC) dysfunction in the aorta contributes to atherosclerosis and complications in vascular grafts, prompting a need for research on its relationship with vascular remodeling.
  • This study developed glutamine synthetase (GS) loaded vascular grafts (GSVG) to enhance endothelial metabolism, showing significant improvements in dysfunctional human umbilical vein endothelial cells (HUVECs) in laboratory tests.
  • Results indicated that GSVG not only improved EC function but also influenced smooth muscle cell behavior, reduced inflammation, and promoted better vascular graft healing in an animal model.
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Stem cell-derived extracellular vesicles (EVs) show great potential for promoting bone tissue regeneration. However, normal EVs (Nor-EVs) have a limited ability to direct tissue-specific regeneration. Therefore, it is necessary to optimize the osteogenic capacity of EV-based systems for repairing extensive bone defects.

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Cell sheet engineering has been proven to be a promising strategy for cardiac remodeling post-myocardial infarction. However, insufficient mechanical strength and low cell retention lead to limited therapeutic efficiency. The thickness and area of artificial cardiac patches also affect their therapeutic efficiency.

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Drug-loaded liposomes have been shown to be effective in the treatment of hepatocellular carcinoma (HCC). However, the systemic non-specific distribution of drug-loaded liposomes in tumor patients is a critical therapeutic challenge. To address this issue, we developed galactosylated chitosan-modified liposomes (GC@Lipo) that could selectively bind to the asialoglycoprotein receptor (ASGPR), which is highly expressed on the membrane surface of HCC cells.

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Implantable tissue-engineered vascular grafts (TEVGs) usually trigger the host reaction which is inextricably linked with the immune system, including blood-material interaction, protein absorption, inflammation, foreign body reaction, and so on. With remarkable progress, the immune response is no longer considered to be entirely harmful to TEVGs, but its therapeutic and impaired effects on angiogenesis and tissue regeneration are parallel. Although the implicated immune mechanisms remain elusive, it is certainly worthwhile to gain detailed knowledge about the function of the individual immune components during angiogenesis and vascular remodeling.

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Translocation of extrinsic molecules into living cells is becoming increasingly crucial in biological studies ranging from cell engineering to biomedical applications. The concerns regarding biosafety and immunogenicity for conventional vectors and physical methods yet challenge effective intracellular delivery. Here, we begin with an overview of approaches for trans-membrane delivery up to now.

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The multi-bacterial environment of the oral cavity makes it hard for periodontal regeneration. As a class of antimicrobial peptide, beta defensin has been found to show broad-spectrum antibacterial ability. In addition, connective tissue growth factor (CTGF) is demonstrated to play a great role in multi-physiological events such as angiogenesis, wound healing and, more importantly, fibrogenesis.

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Quercetin (Que) has been proved to have various biological activities, including anti-oxidation, anti-inflammation and anti-virus, showing great potential in liver protection. However, its water insolubility leads to low bioavailability. Therefore, the development of a suitable drug delivery fashion is imminent.

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Critical limb ischemia (CLI) is the most severe clinical manifestation of peripheral arterial disease, which causes many amputations and deaths. Conventional treatment strategies for CLI (e.g.

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Ternary heterostructured nanofibers (NFs) consisting of plasmonic noble metal nanoparticles (Au, Ag, or Pt NPs), graphitic carbon nitride nanosheets (g-C3N4 NSs), and TiO2 NPs were synthesized in situ via a facile electrospinning technique combined with a subsequent thermal oxidation/reduction process. The thermal-reduced plasmonic NPs with sizes from 5 to 10 nm are dispersed uniformly into the heterojunctions of the NFs that are formed by thermal oxidation etching of exfoliated g-C3N4 NSs in the electrospun TiO2 nanofibrous matrix, as evidenced by microscopic and electronic structure analyses. In comparison to single-component photocatalysts, such as g-C3N4 NSs or TiO2 NFs, these ternary heterostructures exhibit significantly high photocatalytic activity for H2 evolution under simulated sunlight irradiation.

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