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Updated: Jun 7, 2026

Co-immunoprecipitation Assay Using Endogenous Nuclear Proteins from Cells Cultured Under Hypoxic Conditions
Published on: August 2, 2018
[The changes in expression of uncoordinated 33-like phosphoprotein 1 and hypoxia-inducible factor-1α in neuroblastoma
1Department of Neurology, the Affiliated Shengjing Hospital, China Medical University, Shenyang 110004, Liaoning, China. tanf@sj-hospital.org
Objective:
To study the differences in expression of uncoordinated 33-like phosphoprotein 1 (Ulip1) and hypoxia-inducible factor-1α (HIF-1α) in neuroblastoma cell lines that have neuronal characteristics under normoxia and hypoxia conditions.
Methods:
Two neuroblastoma cell lines (KCNR and BE2) which had neuronal characteristics were used in this study. The neuroblastoma cells were cultured under normoxic (20% of oxygen) or hypoxic (1% of oxygen) conditions for 4 hours, then cells were harvested and proteins were extracted. Western blotting was used to detect the levels of Ulip1 and HIF-1α.
Results:
After 4-hour hypoxia treatment, the expression of HIF-1α increased significantly in both cell lines, while the expression of Ulip1a and Ulip1b, which were two isoforms of Ulip1, decreased. There was an 1.6-fold increase of HIF-1α expression in KCNR cells and 2.9-fold increase in BE2 cells; for Ulip1a expression, there was a 55% decrease in KCNR cells and a 20% decrease in BE2 cells; for Ulip1b expression, there was a 44% decrease in KCNR cells and a 13% decrease in BE2 cells.
Conclusion:
Ulip1 maybe involved in the hypoxia-induced damage or repair processes in neuronal cells through HIF-1α.
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