Table 1.

Calcineurin mediates reactivation of Kaposi sarcoma–associated herpesvirus in dermal microvascular endothelial cells

PF-8gpK8.1
+ CsA+ CsA
Unstimulated 3.2 ± 2.7 3.4 ± 2.4 < 1 < 1 
Iono 2.9 ± 2.4 3.0 ± 1.8 < 1 < 1 
TPA 8.3 ± 2.3 8.5 ± 2.0 1.5 ± 0.2 1.5 ± 0.1 
TPA + Iono  32 ± 4.6* 7.9 ± 3.4 8.3 ± 3.3* 1.3 ± 0.1 
PF-8gpK8.1
+ CsA+ CsA
Unstimulated 3.2 ± 2.7 3.4 ± 2.4 < 1 < 1 
Iono 2.9 ± 2.4 3.0 ± 1.8 < 1 < 1 
TPA 8.3 ± 2.3 8.5 ± 2.0 1.5 ± 0.2 1.5 ± 0.1 
TPA + Iono  32 ± 4.6* 7.9 ± 3.4 8.3 ± 3.3* 1.3 ± 0.1 

Immortalized DMVEC monolayers were infected with KSHV and stimulated with ionomycin, low-dose TPA, or both in the presence or absence of CsA. After 3 days, the percentage of DMVEC expressing either PF-8 or gpK8.1 was determined. Data shown are mean ± SD of 5 (PF-8 expression) or 10 (gpK8.1 expression) fields.

CsA indicates cyclosporine; iono, ionomycin; TPA, 2-O-tetradecanoyl-phorbol-13-acetate; DMVEC, dermal microvascular endothelial cells; KSHV, Kaposi sarcoma–associated herpesvirus.

*

P < .001 compared to induction by TPA only.

P < .001 compared to induction by TPA + ionomycin in the absence of CsA.

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