Fig. 5.
Fig. 5. RT-PCR analysis of VEGF-A mRNA splice variants synthesized by HIV-1–infected HUT 78 cells. RT-PCR was performed with specific primers, which allow discrimination of the different splice variants of VEGF-A mRNA by the length of the polymerization products. As a control, PCR products obtained with cDNA of a human epithelial cell line (A 431) known to produce VEGF-A are shown (A). The two splice variants coding for the secreted forms of VEGF-A, VEGF121and VEGF165 (131- and 263-bp amplification products) and the cell-associated VEGF189 (335 bp) were found to be synthesized in HUT 78 cells infected with HIV-1 (B). The PCR product corresponding to the mRNA splice variant encoding VEGF165was the most prominent, the one corresponding to VEGF121could be detected to a lesser extent, and the one corresponding to VEGF189 was only present in minimal amounts.

RT-PCR analysis of VEGF-A mRNA splice variants synthesized by HIV-1–infected HUT 78 cells. RT-PCR was performed with specific primers, which allow discrimination of the different splice variants of VEGF-A mRNA by the length of the polymerization products. As a control, PCR products obtained with cDNA of a human epithelial cell line (A 431) known to produce VEGF-A are shown (A). The two splice variants coding for the secreted forms of VEGF-A, VEGF121and VEGF165 (131- and 263-bp amplification products) and the cell-associated VEGF189 (335 bp) were found to be synthesized in HUT 78 cells infected with HIV-1 (B). The PCR product corresponding to the mRNA splice variant encoding VEGF165was the most prominent, the one corresponding to VEGF121could be detected to a lesser extent, and the one corresponding to VEGF189 was only present in minimal amounts.

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