TM4

Cat.No.: CSC-C9739L

Species: Mus musculus (Mouse)

Source: Testis

Morphology: epithelial

Culture Properties: monolayer

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Cat.No.
CSC-C9739L
Description
Species: mouse - male, 11 to 13 days old
Strain: BALB/c nu/+
Receptor: follicle stimulating hormone (FSH); androgen; estrogen; progesterone
Histocompatibility: H-Y
Production: transferrin; H-Y antigen; retinol binding protein; plasminogen activator
Histopathology: normal
Note: the TM4 cell line responds to FSH with an increase in cAMP production, but does not respond to luteinizing hormone (LH); the FSH responsiveness is much reduced compared to primary Sertoli cell cultures; constitutive plasminogen activator production is low, but is stimulated by FSH and, to a greater extent, by retinoic acid; tested and found negative for ectromelia virus (mousepox)
Species
Mus musculus (Mouse)
Source
Testis
Recommended Medium
Culture Properties
monolayer
Morphology
epithelial
Quality Control
Tests for mycoplasma, bacteria and fungi were negative
Storage and Shipping
Frozen with 52.5% RPMI-1640, 40% FBS, 7.5% DMSO at about 4-5 x 10^6 cells/ampoule; ship in dry ice; store in liquid nitrogen
Synonyms
TM-4
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.

TM4 Cells are immortalized mouse Sertoli cells isolated from the testes of prepubertal mice and used as an in vitro model system for testicular biology and spermatogenesis. In culture, TM4 cells grow adherently and show epithelial like morphology. They contact each other through tight cell-cell interactions and form confluent monolayers. TM4 Cells express Sertoli cell markers and functional proteins that characterize the Sertoli cell phenotype including markers of the supportive nature of Sertoli cells (vimentin, transferrin) cell adhesion proteins (androgen receptor or AR) and proteins that participate in forming tight junctions (occludin and claudins). Like primary Sertoli cells, TM4 cells also produce many growth factors, cytokines and hormones important for germ cell survival and differentiation.

TM4 cells have been used to study aspects of Sertoli cell biology including cell-cell interactions in the testis and regulation of spermatogenesis. TM4 cells are used to study hormonal regulation of Sertoli cells (androgen and FSH signaling), oxidative stress, apoptosis and cellular toxicology. In particular, they are one of the most common models used in reproductive toxicology and endocrine disruption assay testing environmental chemicals, pharmaceuticals, or nanoparticles for male reproductive toxicity.

Effects of RSV on ZEA-Induced TM4 Cytotoxicity

Zearalenone (ZEA) is one of the most prevalent mycotoxins. ZEA exposure could cause oxidative stress (OS) and male reproductive dysfunctions in animals. Resveratrol (RSV) is an antioxidant and activated Nrf2 by the PI3K/Akt pathway to protect cells from injury. Xu's team aimed to determine whether RSV could protect against ZEA-induced OS and apoptosis in TM4 cells and further explored the underlying mechanism. LY294002, an inhibitor of PI3K/Akt signaling, was used.

TM4 cells were cultured with serial concentrations of ZEA and RSV, respectively, followed by CCK-8 assay. Cell viability decreased in response to the increment of ZEA concentrations (all concentrations ≥10 μmol·L⁻¹, p < 0.05) (Fig. 1A). RSV showed slight inhibition on TM4 cell viability at high concentrations and significant inhibition at 5 and 7.5 μmol·L⁻¹ (p < 0.05) (Fig. 1B). More importantly, 2.5 μmol·L⁻¹ RSV pretreatment rescued ZEA-induced cytotoxicity significantly (p < 0.05) (Fig. 1C). Therefore, 2.5 μmol·L⁻¹ and 20 μmol·L⁻¹ RSV were chosen for the following experiments.

Effects of RSV on ZEA-induced TM4 cytotoxicity. TM4 cells were seeded into a 96-well plate, and the viability analysis of TM4 cells was measured by CCK-8 assay.

Fig. 1. Effects of RSV on ZEA-induced TM4 cytotoxicity. TM4 cells were seeded into a 96-well plate, and the viability analysis of TM4 cells was measured by CCK-8 assay (Liu W, Zheng H, et al., 2022).

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