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QIAN Yujun, QIN Chunxia, SUN Lili, DING Huamin, LI Tiejun. A cell model for high-throughput screening lead compounds targeting HIF-1α for atherosclerosis treatment[J]. Journal of Pharmaceutical Practice and Service, 2019, 37(1): 27-31. doi: 10.3969/j.issn.1006-0111.2019.01.007
Citation: QIAN Yujun, QIN Chunxia, SUN Lili, DING Huamin, LI Tiejun. A cell model for high-throughput screening lead compounds targeting HIF-1α for atherosclerosis treatment[J]. Journal of Pharmaceutical Practice and Service, 2019, 37(1): 27-31. doi: 10.3969/j.issn.1006-0111.2019.01.007

A cell model for high-throughput screening lead compounds targeting HIF-1α for atherosclerosis treatment

doi: 10.3969/j.issn.1006-0111.2019.01.007
  • Received Date: 2018-06-11
  • Rev Recd Date: 2018-09-25
  • Objective To establish a high-throughput in-vitro screening cell model for anti-atherosclerosis leading compounds. Methods Hypoxia response element (HRE) was cloned into a luciferase reporter vector, pGL3-Enhancer, to construct pGL3-HIF-1α-HRE. The THP-1 human monocyte cell line was infected with the pGL3-HIF-1α-HRE and a stable cell line, THP-1-HIF-1α-HRE, was screened. Results Real-time PCR assay showed that HIF-1α expression and luciferase activity in THP-1-HIF-1α-HRE cells was effectively upregulated by hypoxia. The increase of HIF-1α expression and luciferase activity induced by hypoxia was significantly inhibited by lovastatin or curcumin. Conclusion THP1-HIF-1α-HRE, an in-vitro cell model for high-throughput screening lead compounds for anti-atherosclerosis (AS) was successfully established.
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A cell model for high-throughput screening lead compounds targeting HIF-1α for atherosclerosis treatment

doi: 10.3969/j.issn.1006-0111.2019.01.007

Abstract: Objective To establish a high-throughput in-vitro screening cell model for anti-atherosclerosis leading compounds. Methods Hypoxia response element (HRE) was cloned into a luciferase reporter vector, pGL3-Enhancer, to construct pGL3-HIF-1α-HRE. The THP-1 human monocyte cell line was infected with the pGL3-HIF-1α-HRE and a stable cell line, THP-1-HIF-1α-HRE, was screened. Results Real-time PCR assay showed that HIF-1α expression and luciferase activity in THP-1-HIF-1α-HRE cells was effectively upregulated by hypoxia. The increase of HIF-1α expression and luciferase activity induced by hypoxia was significantly inhibited by lovastatin or curcumin. Conclusion THP1-HIF-1α-HRE, an in-vitro cell model for high-throughput screening lead compounds for anti-atherosclerosis (AS) was successfully established.

QIAN Yujun, QIN Chunxia, SUN Lili, DING Huamin, LI Tiejun. A cell model for high-throughput screening lead compounds targeting HIF-1α for atherosclerosis treatment[J]. Journal of Pharmaceutical Practice and Service, 2019, 37(1): 27-31. doi: 10.3969/j.issn.1006-0111.2019.01.007
Citation: QIAN Yujun, QIN Chunxia, SUN Lili, DING Huamin, LI Tiejun. A cell model for high-throughput screening lead compounds targeting HIF-1α for atherosclerosis treatment[J]. Journal of Pharmaceutical Practice and Service, 2019, 37(1): 27-31. doi: 10.3969/j.issn.1006-0111.2019.01.007
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