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Analysis of the Expression of Mir-34A, Mir-199A, Mir-30C and Mir-19A in Peripheral Blood Cd4+T Lymphocytes of Relapsing-Remitting Multiple Sclerosis Patients Publisher Pubmed



Ghadiri N1, 6 ; Emamnia N2, 3, 6 ; Ganjalikhanihakemi M4 ; Ghaedi K5, 6 ; Etemadifar M8 ; Salehi M7 ; Shirzad H1 ; Nasresfahani MH6
Authors
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Authors Affiliations
  1. 1. Immunology Department, School of Medicine, Shahrekord University of Medical Sciences, Shahrekord, Iran
  2. 2. Pediatric Inherited Diseases Research Center, Research Institute for Primordial Prevention of Non-affiliation communicable disease, Isfahan University of Medical Sciences, Isfahan, Iran
  3. 3. Department of Biology, Nour-e Danesh Institute of Higher Education, Meimeh, Iran
  4. 4. Immunology Department, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran
  5. 5. Division of Cellular and Molecular Biology, Department of Biology, Faculty of Sciences, University of Isfahan, Isfahan, Iran
  6. 6. Department of Cellular Biotechnology at Cell Science research Center, Royan Institute for Biotechnology, ACECR, Isfahan, Iran
  7. 7. Department of Genetics, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran
  8. 8. Department of Neurosciences, Al-Zahra Hospital, Isfahan University of Medical Science, Isfahan, Iran

Source: Gene Published:2018


Abstract

Background: Multiple sclerosis is an immune-mediated inflammatory disease of central nervous system. MicroRNAs play important roles in autoimmune diseases such as MS. Objectives: The aim was to evaluate the expression pattern of miR-34a, miR-199a, miR-30c and miR-19a in peripheral blood derived CD4+ T lymphocytes of both relapsing and remitting phases of MS. Methods: Blood samples from 40 RRMS patients (20 in relapsing and 20 in remitting phase) and 20 healthy volunteers were taken. CD4+ T cells were isolated. The expression level of miR-34a, miR-199a, miR-30c and miR-19a, and the percentage of Th17 and Treg cells were measured. Expression of master transcription factors of Th17 and Treg cells and several targets of these miRNAs were also evaluated. Results: Data indicated an increased expression of miR-34a, miR-30c and miR-19a in relapsing phase and decreased expression of miR-199a in remitting phase. ROC curve data add other prestigious information of miR-34a, miR-199a, miR-30c and miR-19a by defining relapsing and remitting phase and also healthy cases with high specificity and sensitivity at a proposed optimum cut-off point. Conclusion: Collectively, we showed a correlation between the four miRNAs with different phases of MS and their possible involvement in differentiation pathways of Th17 cells, as the most important players in MS. © 2018
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