Immortalized Human Conjuctival Epithelial Cells-SV40

Cat.No.: CSC-I9101L

Species: Homo sapiens

Source: Eye

Morphology: Polygonal

Culture Properties: Adherent

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Cat.No.
CSC-I9101L
Description
Species
Homo sapiens
Source
Eye
Culture Properties
Adherent
Morphology
Polygonal
Immortalization Method
Serial passaging and transduction with recombinant lentiviruses carrying SV40 Large T antigen
Application
For Research Use Only
Storage
Directly and immediately transfer cells from dry ice to liquid nitrogen upon receiving and keep the cells in liquid nitrogen until cell culture needed for experiments.

Note: Never can cells be kept at -20 °C.
Shipping
Dry Ice.
Recommended Products
CIK-HT003 HT® Lenti-SV40T Immortalization Kit
Quality Control
Real Time PCR was used to quantify SV40 gene expression in immortalized cell line.
BioSafety Level
II
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.

Generated from primary human conjunctival epithelium, immortalized human conjunctival epithelial cells-SV40 are able to proliferate indefinitely due to genetic modification induced by the introduction of the SV40 big T antigen. Bypassing replicative senescence, the immortalization process maintains epithelial polarity, mucin synthesis, and the ability to create a barrier, all of which are hallmarks of native conjunctival epithelial cells. Consequently, they offer a reliable and repeatable in vitro model that circumvents the short life span and inherent variability of original cultures. These cells are commonly utilized in ocular surface research to study epithelial physiology, inflammatory responses, and disease causes such as dry eye, allergic conjunctivitis, and infectious diseases. Research into cytokine signaling, cell-cell interactions, and the consequences of environmental stresses including oxidative damage and desiccation may all be accomplished using these assays. Furthermore, Immortalized Human Conjunctival Epithelial Cells-SV40 provide a useful platform for assessing ocular formulations, screening drugs for toxicity, and conducting drug screenings.

Immortalized Human Conjunctival Epithelial Cells Produce Functional Complement C3 and C4 Proteins

The complement system is crucial for ocular surface immunity, however it is uncertain whether conjunctival epithelial cells generate complement proteins. Ziemanski et al. investigated whether immortalized human conjunctival epithelial cells (HCjE) generate the complement proteins C3 and C4.

To assess C3 and C4 secretion by HCjE, supernatants from undifferentiated and differentiated cells were examined. C3 was identified in both circumstances but not in media controls, with differentiated HCjE secreting 9.77-fold more than undifferentiated cells (556.55 ± 91.75 vs. 56.95 ± 12.09 ng/ml, p < 0.001) (Fig. 1A). C4 levels were significantly reduced in all samples, with a peak in differentiated HCjE supernatants (0.599 ± 0.476 ng/ml) (Fig. 1B). The cell lysate analysis corroborated these findings. Differentiated HCjE had 3.25 times more cellular C3 than undifferentiated cells (0.585 ± 0.183 vs. 0.180 ± 0.102 ng/μg protein, p < 0.001) (Fig. 2A). In contrast, cellular C4 was 3.95-fold lower in differentiated vs undifferentiated lysates (0.00202 ± 0.00016 vs. 0.00797 ± 0.00487 ng/μg protein, p < 0.001) (Fig. 2B).

C3 and C4 from HCjE Supernatants HCjE were cultured under undifferentiating (UNDIFF, serum-free) and differentiating (DIFF, 10% heat-inactivated serum) conditions

Fig. 1. C3 and C4 from HCjE Supernatants HCjE were cultured under undifferentiating (UNDIFF, serum-free) and differentiating (DIFF, 10% heat-inactivated serum) conditions (Zeimanski J F and Szalai A J, 2024).

C3 and C4 from HCjE Cell Lysates HCjE were cultured under undifferentiating (UNDIFF, serum-free) and differentiating (DIFF, 10% heat-inactivated serum) conditions (see Methods) and used to prepare HCjE cell lysates for analysis of C3 and C4 fractions, defined to be total [C3 or C4] per ug of total cellular protein

Fig. 2. C3 and C4 from HCjE Cell Lysates HCjE were cultured under undifferentiating (UNDIFF, serum-free) and differentiating (DIFF, 10% heat-inactivated serum) conditions (see Methods) and used to prepare HCjE cell lysates for analysis of C3 and C4 fractions, defined to be total [C3 or C4] per ug of total cellular protein (Zeimanski J F and Szalai A J, 2024).

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