Fereshteh Dalouchi - Physiology Research Center, Iran University of Medical Sciences, Tehran, Iran.
Zeynab Sharifi Aghdam - Physiology Research Center, Iran University of Medical Sciences, Tehran, Iran
Raza Falak - Department of Immunology, School of Medicine, Iran University of Medical Sciences, Tehran, Iran
Morteza Bakhshesh - Khomein University of Medical Sciences, Khomein, Iran
Maryam Hajidazeh - Department of Immunology, School of Medicine, Iran University of Medical Sciences, Tehran, Iran
Maryam Naseroleslami - Department of Cellular and Molecular Biology, Faculty of Advanced Science and Technology, ‎Tehran Medical Sciences, Islamic Azad University, Tehran, Iran.
Mahdieh Mehrab Mohseni - Department of Cellular and Molecular Biology, Faculty of Advanced Science and Technology, Tehran Medical Sciences, Islamic Azad University, Tehran, Iran
Yaser Azizi - Physiology Research Center, Iran University of Medical Sciences, Tehran, Iran.
Nahid Aboutaleb - Physiology Research Center, Iran University of Medical Sciences, Tehran, Iran.

Background: A lot of patients are suffering from asthma. For decreasing the asthma symptoms, we studied the effects of conditioned medium (CM) of human amniotic membrane mesenchymal stem cells (hAM-MSCs) as a source of anti-inflammatory cytokines on splenocyte and lung tissue of asthmatic Balb/c mice.Methods: Forty mice were categorized into four groups; ovalbumin (OVA)-induced asthma, CM-treated asthma, DMEM (Dulbecco's Modified Eagle Medium)-treated asthma, and saline control. Each group received related treatment. The lung alpha-smooth muscle actin (α-SMA)  and splenocyte inflammatory cytokines and IgE were examined through Western blot analysis.Results: Western blot showed α-SMA overexpression in the OVA and DMEM groups compared with the saline group. CM therapy could significantly reverse it compared with OVA and OVA+DMEM categories by elevating IL-۱۰ and IFN-γ and reducing IL-۴, IgE, and TGF-β .Conclusion: CM treatment could improve asthma symptoms by adjusting α-SMA in lung tissue and pro-inflammatory cytokines and IgE in splenocytes.

Asthma, Alpha-smooth muscle actin, Mesenchymal stem cell