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Single cell analysis of switch-like induction of CYP1A1 in liver cell lines.

Authors
Broccardo-CJ; Billings-RE; Chubb-LS; Andersen-ME; Hanneman-WH
Source
Toxicol Sci 2004 Apr; 78(2):287-294
NIOSHTIC No.
20035684
Abstract
The shape of the dose-response curve may vary depending on whether one examines response at a population or a single cell level. Populations of cells may exhibit a graded response whereas single cell responses may have threshold or switch-like behavior. Studies in vivo and in vitro using primary hepatocyte cultures have shown that induction of CYP1A1 in the liver exhibits switch-like behavior in response to PCB 126 (3,3',4,4',5-pentachlorobiphenyl). The goal of the present study was to determine if two liver cell lines (H4IIE rat hepatoma and Hepa 1c1c7 mouse hepatoma) also show switch-like behavior and develop experimental models for studying mechanisms of these switch-like responses. Both cell lines were analyzed via concentration-response and time-course studies using quantitative real-time PCR, revealing a sigmoidal concentration-response curve for CYP1A1 mRNA induction at the population level. To study CYP1A1 protein induction on a single cell level, flow cytometry was employed. In both cell lines the distribution of fluorescence increased with increasing concentrations of PCB 126. The switch behavior was more pronounced in the H4IIE cells than in the Hepa 1c1c7 cells, exhibiting a well-defined shift of induction from the "off" to the "on" state. The concentration-response curve at the single cell level appeared more switch-like with two populations of cells-basal levels and maximally induced. Immunocytochemistry studies of individual cells also support these conclusions. Our data support the hypothesis that PCB 126 induces CYP1A1 in a switch-like fashion in H4IIE rat hepatoma cells. These cells can now be used to study the mechanism of the biological switch.
Keywords
Cytotoxicity; Cytotoxins; Dose-response; Dosimetry; Cell-biology; Cell-cultures; Cell-function; Cell-metabolism; Cell-morphology; Cell-transformation; Cellular-function; Cellular-reactions; Cellular-structures; Animal-studies; Animals; Liver; Liver-cells; Liver-function; Liver-tissue; Chemical-composition; Chemical-inhibition; Chemical-properties; Chemical-reactions; Chemical-structure; Chemical-synthesis; Author Keywords: PCB; CYP1A1; switch; flow cytometry; H4IIE; Hepa 1c1c7
Contact
C. J. Broccardo, Department of Environmental and Radiological Health Sciences, Colorado State University, Fort Collins, Colorado 80523-1680
CODEN
TOSCF2
CAS No.
11097-69-1
Publication Date
20040401
Document Type
Journal Article
Email Address
hanneman@colostate.edu
Funding Type
Cooperative Agreement
Fiscal Year
2004
NTIS Accession No.
NTIS Price
Identifying No.
Cooperative-Agreement-Number-U50-OH-007545
Issue of Publication
2
ISSN
1096-6080
Source Name
Toxicological Sciences
State
CO; NC
Performing Organization
Colorado State University - Fort Collins
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