Abstract

Objective: To explore the correlations between miR-125b, miR-200c, and the severity of interstitial lung disease associated with dermatomyositis/polymyositis (DM/PM-ILD). Methods: 30 consecutive patients with DM/PM and 23 healthy controls were recruited into current study. Anti-JO-1, anti-SSA, muscle enzymes, the data of chest HRCT and pulmonary function test were collected. 9 consecutive DM/PM-ILD patients underwent bronchoalveolar lavage (BAL). TGF-β1 and surfactant protein D (SP-D) in BAL fluid (BALF) and plasma were detected by ELISA. miR-125b and miR-200c in PBMCs and bronchoalveolar cells were detected by QRT-PCR. All patients were classified into three groups: Mild or non-ILD group, moderate ILD group, and severe ILD group. The correlations between miRNAs and the severity of ILD, the lung damage markers, auto-antibodies, were analyzed. Results: The levels of miR-125b and miR-200c in bronchoalveolar cells were higher than in PBMCs, and the levels of TGF-β1 and SP-D were higher in BALF than in plasma in DM/PM-ILD patients. There were positive correlations between miR-125b, miR-200c in bronchoalveolar cells and SP-D in BALF. The levels of miR-125b and miR-200c in severe ILD group were higher than in mild or non-ILD and moderate ILD groups. There were negative correlations between miR-125b, miR-200c, and FEV1, and between miR-200c and DLCO. The patients with anti-JO-1 antibody had higher levels of miR-125b and miR-200c, and had more severe condition of ILD. Conclusion: miR-125b and miR-200c were positively correlated with the lung damage and severity of ILD in DM/PM, which could be important markers for judgement of disease condition in clinic.

Highlights

  • Interstitial lung disease (ILD) is often shown as fibrosis and deposit of extracellular matrix in high resolution computerized tomography (HRCT) and pathology

  • TGF-β1 and surfactant protein D (SP-D) in bronchoalveolar lavage (BAL) fluid (BALF) and plasma were detected by ELISA. miR-125b and miR-200c in peripheral blood mononuclear cells (PBMCs) and bronchoalveolar cells were detected by quantitative reverse transcription-polymerase chain reaction (QRT-PCR)

  • We reported the association between miR-125b, miR-200c and clinical parameters associated with ILD in DM/PM, such as chest HRCT, pulmonary function test (PFT), and the parameters of lung damage, surfactant protein D (SP-D) and transforming growth factor beta1 (TGF-β1)

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Summary

Introduction

Interstitial lung disease (ILD) is often shown as fibrosis and deposit of extracellular matrix in high resolution computerized tomography (HRCT) and pathology. MicroRNAs (miRNAs) are small non-coding RNAs that are generally believed involved in regulating the expression of protein-encoding genes by blocking the translation or inducing degradation of target mRNAs [3]. MiR-200c plays a crucial role in keeping the phenotype of AECs and inhibiting of lung fibrosis [8]. MiR-125b protected the lung in model mouse of acute lung injury by reducing the counts of total cells, proinflammatory cytokines and chemokines in bronchoalveolar lavage fluid (BALF) [10]. In these diseases, miR-125b works mainly through affecting proliferation, differentiation, metastasis of different types of cells

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