AI Article Synopsis

  • Muscle satellite cells (MuSCs) are essential for muscle growth and repair, and primary pig MuSCs (pMuSCs) serve as a key model for research in pig muscle development.
  • Long-term culture of pMuSCs loses their stemness, which hampers research; to solve this, scientists created immortalized pMuSCs (SV40 T-pMuSCs) using a lentiviral vector that allows them to be cultured for over 40 generations.
  • SV40 T-pMuSCs show similar growth to primary cells initially but have slightly reduced differentiation potential, which can be improved by silencing SV40 T-antigen expression, making them a valuable resource for studying pig skeletal muscle.

Article Abstract

Muscle satellite cells (MuSCs) are crucial for muscle development and regeneration. The primary pig MuSCs (pMuSCs) is an ideal in vitro cell model for studying the pig's muscle development and differentiation. However, the long-term in vitro culture of pMuSCs results in the gradual loss of their stemness, thereby limiting their application. To address this conundrum and maintain the normal function of pMuSCs during in vitro passaging, we generated an immortalized pMuSCs (SV40 T-pMuSCs) by stably expressing SV40 T-antigen (SV40 T) using a lentiviral-based vector system. 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, our results provide a valuable tool for studying pig skeletal muscle development and differentiation.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11049531PMC
http://dx.doi.org/10.3390/cells13080703DOI Listing

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