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- 저자 : Guoliang Lei (검색결과 3 건)
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Guoliang Jiang,Lei Zhang,Jinkun Wang,Houjun Zhou 한국통합생물학회 2016 Animal cells and systems Vol.20 No.5
Glioblastoma (GBM) is the most aggressive cerebral gliomas. Moreover, the overall prognosis of GBM is still little. Baicalein (BA) is a flavonoid derived from the Scutellaria baicalensis root, and has historically been used in anticancer therapies. However, its apoptosis role and related mechanisms in GBM has not yet been researched clearly. Thus, this study aimed to investigate the effects of BA on human GBM U251 cell line. The effects of BA on proliferation of U251 cells were measured by Cell Counting Kit-8 assay. Cellular apoptosis was detected by flow cytometry with annexin V-FITC/propidium iodide staining. The expression of apoptosis-related protein Bcl-2, Bax and cleaved-caspase3 was detected by quantitative real-time PCR and western blot. The expression of nuclear p65 protein, the active subunit of nuclear factor-kappa B (NF-κB), was determined by immunofluorescence and western blot. Our results showed that the viability of U251 cells significantly decreased in a time- and dose-dependent manner after treated with BA, and the apoptotic ratio of BA-treated groups was significantly higher than that of control groups. Furthermore, the expression of NF-kB-p65 in the nucleus was remarkably reduced, and the activity of NF-kB-p65 was remarkably inhibited after BA treatment. Combined treatment with a NF-kB-P65 inhibitor (QNZ) and BA resulted in the synergistic reduction of Bcl-2 expression and then increase of Bax and cleaved-caspase3 expression; and the viability of U251 cells was also inhibited. In conclusion, BA inhibits GBM cells viability and induces apoptosis via inhibit the activity of NF-kB-p65, suggesting that BA is a potential therapeutic agent for GBM.
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Wenxiang Zhang,Hucai Zhang,Jie Niu,Guoliang Lei,Fengqin Chang 한국지질과학협의회 2020 Geosciences Journal Vol.24 No.6
Lacustrine deposits can provide insight into chemical weathering and climate change. Based on the analysis of the element concentrations and parameters of the acid-leaching residual fractions (AR) in the lacustrine deposits of the Qaidam Basin (QB), chemical weathering and paleoclimate changes in the northeastern Tibetan Plateau (NETP) have been studied. The results show that the characteristics of trace element concentrations exhibit two kinds of patterns by normalized element arbitrary units (a.u.). The rare earth element (REE) distribution patterns are moderately rich in light rare earth elements (LREEs) with slightly right-tilting and negative Eu anomalies. Triangular plots of the REEs and (La/Yb)n-ΣREE suggest that the sediments have a similar source. The geochemical records of climate proxies indicated warm-wet climate stages during 45.1–31.6 cal. ka BP., further proving that a megalake stage existed in the semi-arid area in marine isotope stage (MIS) 3. Strong evaporation resulted in a high paleolake level history in the northeastern Tibetan Plateau after the late period of MIS 3. Meanwhile, the geochemical records of the Qaidam Basin are synchronous with the global records.
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Tao, Yong,Fu, Zhuo,Xia, Guoliang,Lei, Lei,Chen, Xiufen,Yang, Jie Asian Australasian Association of Animal Productio 2005 Animal Bioscience Vol.18 No.5
Nitric oxide (NO) derived from inducible nitric oxide synthase (iNOS) is involved in cell apoptosis, which contributes to luteal regression and luteolysis in some species. In large domestic animals, no direct evidence for the relationship between NO and cell apoptosis in the process of corpus luteum regression is reported. The present study was conducted to investigate the localization of iNOS on porcine corpora lutea (CL) during the oestrus cycle and its relation to cell DNA fragmentation and CL regression. According to morphology, four luteal phases throughout the estrous cycle were defined as CL1, CL2, CL3 and CL4. By isoform-specific antibody against iNOS, the immunochemial staining was determined. Luteal cell DNA fragmentation was determined by flow cytometry. The results showed that no positive staining for iNOS was in CL1 and that iNOS was produced but limited to the periphery of CL2, while in the CL3, the spreading immunochemical staining was found inside the CL. No iNOS positive staining was detected in CL4. Meanwhile, DNA fragmentation increased dramatically when CL developed from CL2 to CL3 (p<0.05). In CL4, higher proportion of luteal cells still had fragmented DNA than that of luteal cells from CL1 or CL2 (p<0.05). These results indicate that iNOS expression is closely related to luteal cell apoptosis and then to luteal regression.
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