Immortalized Human Lens Epithelial Cells-SV40

Cat.No.: CSC-I9160L

Species: Homo sapiens

Source: Infant lens

Morphology: Polygonal

Culture Properties: Adherent

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Cat.No.
CSC-I9160L
Description
The Immortalized Lens Epithelial Cells - SV40 is established from primary cells (isolated from infant lens epithelial fragments) using adenovirus-SV40 virus. The Immortalized Human Lens Epithelial Cells - SV40 provides a homogeneous population of cell for the investigation of the physiology of the normal human lens epithelium and study its response to cataractogenic agents and the human lens specific functions. These cells also provide a unique system for examining the relationship between gene expression and differentiation.
Species
Homo sapiens
Source
Infant lens
Culture Properties
Adherent
Morphology
Polygonal
Immortalization Method
Serial passaging and transduction with recombinant adenovirus 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
CSC-7764W Human Lens Epithelial Cells (HLEpiC)
CIK-HT003 HT® Lenti-SV40T Immortalization Kit
Quality Control
The Immortalized Human Lens Epithelial Cells react positively with the monoclonal antibody to SV40 large T antigen. Western blot and precipitation are used to confirm the presence of βH- and γ-crystallin, the proteins that are markers for cell differentiation in the lens epithelium.
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.

Immortalized Human Lens Epithelial Cells-SV40 (HLE-SV40) are a human epithelial cell line, which have been immortalized with SV40 large T antigen and are derived from the anterior lens capsule of human donor tissue. HLE-SV40 cells preserve a majority of the native lens epithelial cell biological properties, including polygonal epithelial morphology and expression of cytokeratins, E-cadherin, and lens-specific crystallins (αA- and β-crystallin). In addition, the immortalized HLE-SV40 cells are proliferatively stable in culture and have a well-defined and reproducible gene expression profile.

HLE-SV40 cells physiologically serve as the anterior-most cell layer of the lens that are crucial for maintenance of lens transparency, ion homeostasis, and fiber cell differentiation. In addition, they are highly responsive to oxidative stress, ultraviolet irradiation, and a number of growth factors and cytokines, many of which are related to or directly stimulate cataractogenesis in vivo. The cells have also been used to investigate epithelial-mesenchymal transition (EMT) in response to TGF-β stimulation. HLE-SV40 cells are therefore frequently used in studies focused on processes related to cataractogenesis and especially the study of posterior capsule opacification (PCO) or fibrosis following cataract surgery.

HLE-SV40 cells have become a staple model system for research focused on cataract, oxidative injury, drug toxicity, regulation of crystallins, and screening anti-cataract therapeutics. Their physiological relevance combined with their robust proliferative capacity in 2D monolayer cultures has made them a widely used cell line in biochemical assays and imaging-based approaches.

Hesperetin (Hst) Treatment and AGE Formation in vitro

Cataracts and presbyopia are age-related conditions linked to increased AGEs in lens proteins. Hesperetin (Hst) has antioxidant and anti-inflammatory properties and has been shown to prevent cataracts and presbyopia. Here, Doki et al. used in vitro human lens epithelial cell lines and ex vivo mouse lens organ cultures to assess Hst's effects on AGE formation and lens protein modification.

The study examined if Hst treatment could affect AGE formation in immortalized human lens epithelial cells (ihLECs). The structural formula of Hst is shown in Fig. 1A. CML, a major AGE compound binding to ihLECs proteins, was detected. High-glucose medium with MGO and ERT stimulated AGE and CML binding to proteins. ihLECs treated with MGO and ERT in high-glucose medium showed significantly increased AGE formation, but Hst treatment inhibited this in a dose-dependent manner (Fig. 1B). Immunohistochemistry staining revealed that high-glucose stimulation increased AGE and CML signals in ihLECs, which were cancelled by Hst treatment (Fig. 2A and B). Thus, Hst can prevent AGE and CML formation in the lens.

Effect of Hst treatment on AGE modifications of lens epithelial cell lines.

Fig. 1. Effect of Hst treatment on AGE modifications of lens epithelial cell lines (Doki Y, Nakazawa Y, et al., 2023).

Effect of Hst treatment on AGE and CML formations in lens epithelial cell lines.

Fig. 2. Effect of Hst treatment on AGE and CML formations in lens epithelial cell lines (Doki Y, Nakazawa Y, et al., 2023).

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