Parisa Zamani Esmati - Department of Biology, Mashhad Branch, Islamic Azad University, Mashhad, Iran.
Javad Baharara - Research Center for Animal Development and Applied Biology, Mashhad Branch, Islamic Azad University, Mashhad, Iran
Sajad Sahab Negah - Neuroscience research center, Mashhad University of Medical Sciences (MUMS), Mashhad, Iran
Khadijeh Nejad Shahrokhabadi - Department of Biology, Mashhad Branch, Islamic Azad University, Mashhad, Iran.

Background: In children with lymphoblastic leukemia (ALL), cancerous metastasis to the central nervous system (CNS) is common, but there is insufficient information on this metastasis and cancer progression process. Further, the role of exosomes on cancer growth and metastasis has been the attention of many studies. Because the astrocytes involve in the blood-brain barrier and stay in contact with peripheral blood , we investigated the effect of exosomes derived Nalm۶ cell line on astrocytes from human brain fetal tissue.    Methods: In this in vitro study, exosomes were isolated from the supernatant of Nalm۶ cell line by centrifugation and identified by DLS, AFM and FE-SEM methods. Astrocytes were isolated from human fetal brain tissue cells and expanded and identified by GFAP antibody with immunocytochemistry. Astrocytes were treated with different concentrations of exosomes (i.e., ۵, ۱۰, ۳۰, and ۵۰ µg/ml),. Proliferation and migration were assessed with Trypan blue staining and scratch methods, respectively. To define tumorogensis changes in astrocytes treated by exosomes, the expression of MMP۹, P۵۳, and Cox۲ genes were investigated by Real-Time PCR.Findings: According to the DLS results, the size of exosomes was about ۴۳ nm. AFM and FE-SEM imaging indicated these exosomes have a spherical shape. Our results showed that the proliferation of astrocytes significantly increased when treated with ۵۰ µg/ml of exosomes.Therefore, the concentration of ۵۰ µg/ml was considered for further experiments. Astrocyte migration was significantly increased compared to the control group. Finally, our results showed tumorogenesis changes in astrocytes by increasing the expression of MMP۹ and Cox۲ and decreasing the expression of p۵۳ at mRNA level.Conclusion: Based on our in vitro study, exosomes derived from ALL as a peripheral tumor can change the behavior of astrocytes as a target for metastasis. Further investigations on this topic are warranted to shed light on metastatic mechanisms.

Leukemia, Exosome, Astrocyte, Tumorigenesis