Evaluation of survivin expression and regulating miRNAs of survivin expression in peripheral blood mononuclear cells in systemic lupus erythematous patients

Author:

Bolouri Nasim12,Mansouri Reza1,Farhadi Elham23,Soltani Samaneh2,Akhtari Maryam4,Madreseh Elham23,Faezi Seyedeh Tahereh2,Jafarinejad-Farsangi Saeideh5,Jamshidi Ahmadreza2,Mahmoudi Mahdi23ORCID

Affiliation:

1. Immunology Department, Shahid Sadoughi University of Medical Sciences, Yazd, Iran

2. Rheumatology Research Center, Tehran University of Medical Sciences, Tehran, Iran

3. Research Center for Chronic Inflammatory Diseases, Tehran University of Medical Sciences, Tehran, Iran

4. Tobacco Prevention and Control Research Center (TPCRC), National Research Institute of Tuberculosis and Lung Diseases (NRITLD), Shahid Beheshti University of Medical Sciences, Tehran, Iran

5. Physiology Research Center, Institute of Neuropharmacology, Kerman University of Medical Sciences, Kerman, Iran

Abstract

Background Systemic lupus erythematosus is a multisystemic rheumatic disease with different clinical features. Disturbance in apoptosis regulation seems to be a major factor in SLE development. Objective Survivin plays a key role in mitosis and inhibiting apoptosis. A study was conducted to examine the expression level of survivin and miRNAs that affect survivin transcript levels in patients with SLE. Methods We isolated peripheral blood mononuclear cells from 50 inactive SLE patients and 50 healthy controls. RNA is extracted and converted to cDNA. The quantitative real‐time polymerase chain reaction is conducted to assess the expression levels of survivin total and its variants with effective miRNAs in PBMCs. Results Expression levels of miR-34a-5p (fold change = 1.5, p ++ = 0.027), and 218-5p (fold change = 1.5, p ++ = 0.020) were significantly increased. While miR-150-5p (fold change = 0.56, p ++ = 0.003) was significantly decreased. The mRNA expression of survivin-WT (fold change = 0.63, p++ = 0.002) was significantly downregulated in SLE patients compared to the healthy controls. Survivin total and its two major variants (survivin-2B, and survivin-ΔEx3) did not differ significantly between SLE patients and controls. Conclusion Although survivin-TS and its two variants (survivin-2B, and survivin-ΔEx3) were not differently expressed in SLE patients, survivin-WT had altered expression. Despite aberrant miRNA expression in PBMCs from SLE patients, survivin and miRNA expression were not associated with leukopenia. The pathogenesis of SLE disorder might be linked to survivin’s other roles in the immune system aside from anti-apoptotic functions.

Funder

Tehran University of Medical Sciences and Health Services

Shahid Sadoughi University of Medical Sciences

Publisher

SAGE Publications

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