Immortalized Porcine Skeletal Muscle Satellite Cells

Cat.No.: CSC-I2067Z

Species: Porcine

Morphology: Polygonal

Culture Properties: Adherent

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  • Background
  • Scientific Data
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Cat.No.
CSC-I2067Z
Description
Porcine Skeletal Muscle Satellite Cells were transfected with SV40LT expressing lentiviral particles. These primary cells go into senescence after the 2nd passage while the Immortalized Skeletal Muscle Satellite Cells go beyond 30 passages.
Species
Porcine
Recommended Medium
SuperCult® Immortalized Porcine Skeletal Muscle Cell Medium (Cat No.: CM-I2067Z)
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.
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.

Muscle satellite cells (MuSCs) are the major cell type involved in skeletal muscle regeneration and are essential for the growth, maintenance, and repair of skeletal muscle after birth. In mature resting muscle, MuSCs mainly remain in a quiescent state. However, upon muscle damage, these cells are activated and undergo self-renewal, proliferation, differentiation, and fusion. Ultimately, they will form new muscle fibers and repair damaged muscle tissue.

Pigs have many advantages in modeling human diseases due to their anatomical and physiological similarities to human beings. Porcine muscle satellite cells (pMuSCs) are crucial for studying skeletal muscle development and regeneration and can also be used to produce cultured meat. Like MuSCs from other species, porcine MuSCs also lose their proliferation and differentiation capabilities during long-term in vitro culture. Furthermore, the isolation of primary cells suffers from drawbacks such as time consumption, labor-intensive procedures, and significant inter-individual variability. Researches on porcine muscle is often limited by the use of primary muscle satellite cells. Therefore, it is necessary to establish porcine muscle satellite cells capable of long-term stable passaging in vitro. To address this challenge and maintain the normal function of pMuSCs during in vitro passage, we generated an Immortalized Porcine Skeletal Muscle Satellite Cells (SV40 T-pMuSCs) by stably expressing SV40 T-antigen using a lentiviral vector system. SV40 T-pMuSCs can provide a valuable source of cells for studying porcine skeletal muscle development and differentiation.

Establishment and Characterization of SV40 T-Antigen Immortalized Porcine Skeletal Muscle Satellite Cells

A common method to establish an immortalized cell line is to transfect the primary cells with SV40 T-antigen gene. In this study, primary muscle satellite cells (MuSCs) were isolated from a 1-day-old Western commercial pig's longissimus dorsi muscle using the differential adhesion method. Subsequently, an immortalized porcine skeletal muscle satellite cell line (SV40 T-pMuSCs) was established by transducing the SV40 T-antigen.

The SV40 T-pMuSCs can be stably sub-cultured for over 40 generations in vitro. An evaluation of SV40 T-pMuSCs was conducted through immunofluorescence staining, quantitative real-time PCR, EdU assay, and SA-β-gal activity. Their proliferation capacity was similar to that of primary pMuSCs at passage 1, and while their differentiation potential was slightly decreased. SiRNA-mediated interference of SV40 T-antigen expression restored the differentiation capability of SV40 T-pMuSCs. Taken together, the results provide a valuable tool for studying pig skeletal muscle development and differentiation.

Immunostaining of SV40 T-pMuSCs at P1, P10, P30, and P40 generations using DAPI, EdU, anti-PAX7 and anti-MyHC antibody.

Fig. 1. Establishment and characterization of SV40 T-pMuSCs (Ni, Mengru, et al., 2024).
How can Immortalized Porcine Skeletal Muscle Satellite Cells enhance my research compared to other cell lines?

These cells offer enhanced reliability, uniformity, and longevity, which are crucial for obtaining consistent and reproducible results. By using CSC-I2067Z cells, researchers can minimize variability and increase the robustness of their experimental outcomes.

Are Immortalized Porcine Skeletal Muscle Satellite Cells suitable for high-throughput screening?

Yes, Immortalized Porcine Skeletal Muscle Satellite Cells are highly suitable for high-throughput screening due to their consistent growth and predictable behavior. This makes them an excellent choice for large-scale drug screening and other high-throughput applications.

How do I know that Immortalized Porcine Skeletal Muscle Satellite Cells are of high quality?

Every batch of Immortalized Porcine Skeletal Muscle Satellite Cells (Cat No.: CSC-I2067Z) undergoes rigorous quality control testing, including assessments of morphology, growth rate, genetic stability, and absence of contaminants. This ensures you receive high-quality cells for your research.

What type of support can I expect after purchasing Immortalized Porcine Skeletal Muscle Satellite Cells?

Our dedicated team of scientists and technical support staff are available to assist you with any questions or issues you may encounter. From initial setup to troubleshooting, we are here to support your research every step of the way.

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For research use only. Not for any other purpose.

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