V-79

Cat.No.: CSC-C2756

Species: Cricetulus griseus (Chinese hamster)

Source: Lung

Morphology: fibroblast

Culture Properties: adherent

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Cat.No.
CSC-C2756
Description
Established after spontaneous transformation of cells isolated from the lung of a normal Chinese hamster (male). The G1 phase in these cells is either absent or very short. Consequently they have been used in studies of the G1 growth period. V79 is well established in toxicology studies. Stability of karyotype and morphology is making them suitable for gene toxicity assays with low background aberrations. The cells do not express endogenous cytochrome P450 and have been used for the insertion and expression of P450 from human, rat, mouse and fish. The cells have a high plating efficiency (80%), and a generation time of 12 to 14 hours. The line was renamed V79 by Elkind in 1958.
Species
Cricetulus griseus (Chinese hamster)
Source
Lung
Recommended Medium
Culture Properties
adherent
Morphology
fibroblast
Karyotype
2n=22
Application
This cell line can be used in studies of X-ray induced damage and repair processes.
Quality Control
Tests for mycoplasma, bacteria and fungi were negative
Storage and Shipping
liquid nitrogen vapor phase
Synonyms
V79; V 79; Strain V; V79-1; GM00215; GM-215; GM00215A; GM16136; UCW 100
Citation Guidance
If you use this products in your scientific publication, it should be cited in the publication as: Creative Bioarray cat no. If your paper has been published, please click here to submit the PubMed ID of your paper to get a coupon.

V-79 cells (also known as V79 or V79-4 cells) are a fibroblast-like Chinese hamster cell line developed from lung fibroblasts of the Chinese hamster Cricetulus griseus. Since their development, V-79 cells have been one of the most commonly used mammalian cell lines for genetic toxicology and radiobiology assays. The cell line has been shown to have a stable karyotype and proliferate quickly with high plating efficiency.

In culture, V-79 cells are an adherent monolayer cell line with rapid doubling time and high clonogenic survival. These cells are used for mutation assays, DNA damage assays, and cell survival assays. Because of their low endogenous metabolic enzyme activity, induction of mutation and DNA damage by test compounds can be easily evaluated either directly or after incubation with an exogenous metabolic activation system like liver S9 fractions. For these reasons, V-79 cells have been commonly used for HPRT gene mutation assays, chromosomal aberration assays, and micronucleus assays.

V-79 cells have been extensively used in research of radiation biology studies along with oxidative stress induction and DNA repair mechanisms. Because of their consistent responses to chemicals and radiation, easy culturability, and stability over extended periods of time, V-79 cells continue to be a preferred in vitro model system for testing cytotoxicity and mutagenicity as well as determining cellular responses to environmental chemicals and therapeutics.

Cytotoxicity and Cell Viability Induced by PM in V-79 Cells

Particulate Matter (PM) in ambient air is a major environmental and health concern. Dubey et al. aimed to comprehensively characterize atmospheric PM fractions by size, composition, and morphology, and assess their oxidative potential, genotoxicity, and mutagenicity near a busy roadside in Lucknow, India.

After being exposed to PM for 24 hours, adherent and settled particulate on the surface of V-79 cells had no visible effects on cellular morphology (Fig. 1a). Cells that were exposed to coarse PM became irregular in shape, shrunken, and lifted off the surface in some cases. PM demonstrated a significant concentration-dependent cytotoxic effect (1-100 µg/ml) after 24 hours of exposure, according to cytotoxicity determined by MTT assay. Coarse PM produced the greatest cytotoxicity when compared to other PM fractions and SRM-1649b (Fig. 1b). There was a significant increase in Trypan blue uptake by cells exposed to PM concentrations of 50, 75, and 100 µg/ml after 24 hours of exposure when compared to the control, demonstrating lower cell viability. Coarse PM-exposed cells displayed the greatest loss in cell viability (Fig. 1c). When compared to untreated control cells, acridine orange staining demonstrated concentration-dependent loss in lysosome membrane integrity. Coarse fraction-exposed cells displayed the greatest loss in membrane integrity (Fig. 1d, e).

Effect of PM on cell viability and morphology of V-79 cells.

Fig. 1. Effect of PM on cell viability and morphology of V-79 cells (Dubey K, Manurya R, et al., 2022).

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