Mesenchymal Stem Cells Promote Caspase Expression in Molt-4 Leukemia Cells Via GSK-3α/B and ERK1/2 Signaling Pathways as a Therapeutic Strategy

Background: Mesenchymal stern cells (MSCs) are considered an interesting tool in cell therapy due to their unique features such as self-renewal, multi-potency, and pluripotency. The multifunctional properties of these cells are being investigated in many studies. The current research examined the influence of MSCs on the Molt-4 cell line as acute lymphoblastic leukemia (ALL) cells. Methods: MSCs were cultured, characterized, and co-cultured with Molt-4 cells in a trans-well system. Then, cultured Molt-4 alone and Molt-4 co-cultured with MSCs (10:1) were collected on day 7 and subjected to western blotting for protein expression assessment. Telomerase activity as well as cell senescence, were investigated by PCR-ELISA TRAP assay and beta-galactosidase activity measurement, respectively. Results: It was found that MSCs resulted in a significant increase in the pro-caspase-8 and cleaved-caspase 8 and 9 expression levels. Furthermore, protein expression levels of GSK-3 alpha/beta and ERK1/2 were significantly decreased. The results also showed that MSCs caused significant decreases and increases in telomerase and beta-galactosidase enzyme activity of Molt-4 cells, respectively. Conclusion: It was concluded that MSCs co-cultured with Molt-4 cells could be involved in the promotion of Molt-4 cell apoptosis and cell senescence via caspase-8, 9 cascade and OSK-3 alpha/beta and ERK1/2 signaling pathways.

Automated summary

The study found that MSCs co-cultured with Molt-4 cells could promote Molt-4 cell apoptosis and cell senescence through certain signaling pathways.