Fig. 1.
Fig. 1. Effect of hypoxia on uPAR protein and mRNA levels in HTR-8/SVneo cells. (A) Analysis of uPAR expression by HTR-8/SVneo cells using flow cytometry showed an average increase of 68% in the mean fluorescence intensity when cells were cultured under hypoxic conditions and labeled with MoAb 3937. This figure is representative of seven independent experiments. (B) Northern blot analysis showed a 2.5-fold increase in uPAR mRNA levels after only 4 hours of hypoxic culture when compared with uPAR mRNA levels in cells cultured under standard conditions. The levels of uPAR transcript increased by fivefold at 6 hours of culture under hypoxia and remained high at 8 and 24 hours. Relative levels of uPAR mRNA were determined with a SigmaGel gel analysis program using 28S rRNA to correct for differences in the amount of RNA loaded onto the gel.

Effect of hypoxia on uPAR protein and mRNA levels in HTR-8/SVneo cells. (A) Analysis of uPAR expression by HTR-8/SVneo cells using flow cytometry showed an average increase of 68% in the mean fluorescence intensity when cells were cultured under hypoxic conditions and labeled with MoAb 3937. This figure is representative of seven independent experiments. (B) Northern blot analysis showed a 2.5-fold increase in uPAR mRNA levels after only 4 hours of hypoxic culture when compared with uPAR mRNA levels in cells cultured under standard conditions. The levels of uPAR transcript increased by fivefold at 6 hours of culture under hypoxia and remained high at 8 and 24 hours. Relative levels of uPAR mRNA were determined with a SigmaGel gel analysis program using 28S rRNA to correct for differences in the amount of RNA loaded onto the gel.

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