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Use of cryopreserved transiently transfected cells in high-throughput pregnane X receptor transactivation assay.
Zhu, Zhengrong; Puglisi, Jaime; Connors, David; Stewart, Jeremy; Herbst, John; Marino, Anthony; Sinz, Michael; O'Connell, Jonathan; Banks, Martyn; Dickinson, Kenneth; Cacace, Angela.
Afiliación
  • Zhu Z; Bristol-Myers Squibb Company, Wallingford, CT 06492, USA. zhengrong.zhu@bms.com
J Biomol Screen ; 12(2): 248-54, 2007 Mar.
Article en En | MEDLINE | ID: mdl-17259590
Cryopreserved, transiently transfected HepG2 cells were compared to freshly transfected HepG2 cells for use in a pregnane X receptor (PXR) transactivation assay. Assay performance was similar for both cell preparations; however, cryopreserved cells demonstrated less interassay variation. Validation with drugs of different PXR activation potencies and efficacies demonstrated an excellent correlation (r(2) > 0.95) between cryopreserved and fresh cells. Cryopreservation did not change the effect of known CYP3A4 inducers that have poor cell permeability, indicating that cryopreservation had little effect on membrane permeability. In addition, cryopreserved HepG2 cells did not exhibit enhanced susceptibility to cytotoxic compounds compared to transiently transfected control cells. The use of cryopreserved cells enables this assay to run with enhanced efficiency.
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Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Bioensayo / Preparaciones Farmacéuticas / Receptores de Esteroides / Criopreservación / Activación Transcripcional Límite: Humans Idioma: En Revista: J Biomol Screen Asunto de la revista: BIOLOGIA MOLECULAR Año: 2007 Tipo del documento: Article País de afiliación: Estados Unidos
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Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Bioensayo / Preparaciones Farmacéuticas / Receptores de Esteroides / Criopreservación / Activación Transcripcional Límite: Humans Idioma: En Revista: J Biomol Screen Asunto de la revista: BIOLOGIA MOLECULAR Año: 2007 Tipo del documento: Article País de afiliación: Estados Unidos
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