Main content area

Therapeutic Potential of Mesenchymal Stem Cells on Early and Late Experimental Hepatic Schistosomiasis Model

El-Shennawy, Shahinaz F., Aaty, Heba E. Abdel, Radwan, Nehal A., Abdel-Hameed, Dina M., Alam-Eldin, Yosra H., El-Ashkar, Ayman M., Abu-Zahra, Fatma A.
The Journal of parasitology 2015 v.101 no.5 pp. 587-597
Schistosoma, Y chromosome, actin, acute course, electron microscopy, females, genes, granuloma, hepatocytes, histopathology, immunohistochemistry, infectious diseases, liver, liver diseases, liver function, long term experiments, males, mice, models, morphometry, muscles, polymerase chain reaction, schistosomiasis, stem cells, therapeutics
Cell-based therapy is emerging as a promising therapeutic approach for a wide range of liver diseases. This study aimed to investigate the regenerative and antifibrotic therapeutic potential of bone marrow-derived mesenchymal stem cells (BM-MSCs) in an early and late experimental hepatic schistosomiasis model. BM-MSCs were isolated from 6-wk-old BALB/c donor male mice, then grown and propagated in culture until cell count was 5–8 × 10⁶/ml. MSCs were then separated and injected into Schistosoma mansoni-infected female BALB/c mice on their 6, 10, 14, and 18 wk post-infection. Mice were sacrificed on the fourth and eighth week after BM-MSCs transplantation in each group. Homing of BM-MSCs was confirmed by PCR detection of male Y-chromosome gene (sry) in the liver tissue of the recipient female mice. The regenerative and antifibrotic potential of BM-MSCs was assessed by histopathological examination, morphometric analysis, electron microscopy, and liver function tests. Schistosoma-infected mice, which were treated with BM-MSCs, showed a decrease in the granuloma size, percentage and density of the fibrotic area, formation of new hepatocytes, and improvement of the liver function tests. Immunohistochemical examination of alpha-smooth muscle actin revealed a significant decrease in the immunoreactive hepatic stellate cells in mice treated with MSCs. Early granulomas (acute infection) showed better response to MSC injection than did later granulomas (chronic infection). Dosing and timing of MSCs transplantation should undergo more investigations in long-term experiments before application to the clinical field. This study is the first to assess and compare the effect of MSCs treatment on early and late granulomas.