Publications by authors named "Gwang-Min Lee"

Article Synopsis
  • Di-butyl phthalate (DBP) is a harmful environmental contaminant, and this study explores the use of a specific strain of Bacillus subtilis (LLS-04) for bio-electrodegradation to effectively reduce DBP levels.
  • The bio-electrodegradation method showed a 98.57% reduction in DBP concentration, outperforming other degradation techniques due to enhanced microbial and enzymatic activity.
  • Toxicity assessments indicated that treated effluent from bio-electrodegradation was significantly less toxic than untreated DBP effluent, suggesting its potential for effective bioremediation of phthalate pollution.
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Aim: To assess the effectiveness of Lentilactobacillus parafarraginis A6-2 cell lysate for the removal of aluminum (Al), which induces neurotoxicity, and its protective effect at cellular level.

Methods And Results: The cell lysate of the selected L. parafarraginis A6-2 strain demonstrated superior Al removal compared to live or dead cells.

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Most of the vascular platforms currently being studied are lab-on-a-chip types that mimic capillary networks and are applied for vascular response analysis in vitro. However, these platforms have a limitation in clearly assessing the physiological phenomena of native blood vessels compared to in vivo evaluation. Here, we developed a simply fabricable tissue-engineered vascular microphysiological platform (TEVMP) with a three-dimensional (3D) vascular structure similar to an artery that can be applied for ex vivo and in vivo evaluation.

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Foxp3 stability of vitamin C-treated induced-regulatory T cells (V-iTregs) is superior to that of conventional iTregs (C-iTregs). However, the role of V-iTregs in allograft rejection under vitamin C-deficient conditions, such as those seen in humans, remains unclear. We aimed to elucidate the role of vitamin C treatment on generation and maintenance of iTregs from gulo knockout (Gulo-KO) mice as well as wild type (WT) mice, and in vitro and in vivo suppressive effects of V-iTregs on heart allograft rejection in either Gulo-KO or WT recipient mice.

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