Immortalized Mouse Peritoneal Mesothelium

Cat.No.: CSC-C12031Z

Species: Mouse

Morphology: Polygonal

Culture Properties: Adherent

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Cat.No.
CSC-C12031Z
Description
The Immortalized Mouse peritoneal mesothelium have been developed with large antigen SV40. The MDM cell line is characterized by a high proliferation rate. The MDM cells are large and planar rapidly covering the plate surface. At higher confluence, the MDM cells may be efficiently used as a feeder layer.
Species
Mouse
Recommended Medium
SuperCult® Immortalized Mouse Peritoneal Mesothelium Medium (Cat No.: CM-C12031Z)
Freezing Medium
Complete medium supplemented with 10% (v/v) DMSO
Culture Properties
Adherent
Morphology
Polygonal
Immortalization Method
SV40 large T antigen
Application
For Research Use Only
Growth Properties
Cells are cultured as a monolayer at 37°C in a humidified atmosphere with 5% CO2.
Shipping
Dry Ice.
Quality Control
Real Time PCR was used to quantify SV40T gene expression in immortalized cell line. Free from contaminations (bacteria incl. mycoplasma, fungi, HIV, HAV, HBV, HCV, Parvo-B19) and cross-contaminations.
Storage and Shipping
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.
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 Mouse Peritoneal Mesothelium cells (MDM) are cells immortalized from the mesothelium that lines the abdominal cavity. Mesothelium in vivo creates a slick surface for organs to move frictionlessly against each other and modulate transport of fluids and cells across the serosal membrane. Like most primary mesothelial cells isolated from mammals, these cells are likely to senesce quickly in vitro. However, due to immortalization, this cell line creates an easily replicable and proliferative source to study the biology of this organ lining in depth. Thus, these cells act as an excellent alternative to primary mesothelial cells from mice.

MDM cells are often used in research laboratories to test chemical compounds toxicity before being tested in complex in vivo models. Whether testing novel fluorescent probes or drug delivery vehicles, immortalized cell lines provide a quick screen for cytotoxic effects. In addition to being used in toxicology assays, this line can be used to probe the mechanism of peritoneal inflammation, MMT, and cell response to dialysis fluids. Because this cell line is representative of healthy mesothelium tissue found in mice, pathology can be easily distinguished when abnormal data points are collected.

Highly Fluorescent Distyrylnaphthalene Derivatives as a Tool for Visualization of Cellular Membranes

Fluorescent imaging is a vital interdisciplinary tool for visualizing real-time biological structures. However, there is an ongoing need for safe, efficient, membrane-specific fluorescent probes to monitor membrane-dependent cellular processes. Suwara et al. synthesized and evaluated a series of distyrylnaphthalene-based conjugated oligoelectrolytes (SN-COEs) as fluorescent dyes.

To assess long-term toxicity, DSNN-derivatives were tested over 48 h (Fig. 1) and 72 h across various cell types, including human cancers (K562, MOLT4, HCT116) and non-cancerous mouse (MDM, NIH/3T3) and human (293T, HUVEC, fibroblasts) lines.

In mouse cells (MDM and NIH/3T3), DSNN-P, DSNN-Mor, and DSNN-POK showed no significant toxicity, maintaining 80%-100% viability (Fig. 1). Conversely, DSNN-DEA, DSNN-NMe3+, DSNN-NH2, and DSNN-Py+ exhibited concentration-dependent toxicity at 1-10 μM (Fig. 1). Among non-cancerous human cells, fibroblasts were the most sensitive to the compounds (Fig. 1).

In vitro cytotoxicity assay results (% of living cells) performed on various cell lines after 48 h of treatment with DSNN-compounds in 1, 5 and 10 μM. The experiments were done in triplicate. The results represent the mean ± standard error [%].

Fig. 1. In vitro cytotoxicity assay results (% of living cells) performed on various cell lines after 48 h of treatment with DSNN-compounds in 1, 5 and 10 μM. The experiments were done in triplicate. The results represent the mean ± standard error [%] (Suwara J, Lukasik B, et al., 2020).

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