Neutrophil MiRNA-128-3p is Decreased During Active Phase of Granulo-matosis with Polyangiitis
Granulomatosis with polyangiitis is a rare chronic inflammatory disease. In this multisystem autoimmune disorder neutrophils cause small vessels necrosis and infiltrate perivascular tissue to form granulomas. Progression of the disease is evaluated by the symptoms score and by a titer of anti-neutro...
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Published in | Current genomics Vol. 16; no. 5; pp. 359 - 365 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
United Arab Emirates
Bentham Science Publishers
01.10.2015
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Abstract | Granulomatosis with polyangiitis is a rare chronic inflammatory disease. In this multisystem autoimmune disorder neutrophils cause small vessels necrosis and infiltrate perivascular tissue to form granulomas. Progression of the disease is evaluated by the symptoms score and by a titer of anti-neutrophil cytoplasm antibodies. Despite glucocorticoid and immunosuppressive therapy, prognosis is complicated by chronic renal insufficiency, hearing loss and skin ulceration. In this preliminary study we tested the hypothesis that altered neutrophil expression of miRNAs can contribute to the cell activation, extracellular traps formation and decreased apoptosis. First we compared a profile of 728 miRNAs expressed in circulating neutrophils of patients with active disease and matched healthy donors. Subsequently, candidate miRNAs were quantified in neutrophils from 16 subjects with active disease, 16 asymptomatic patients at the remission and in 16 healthy controls. Out of 11 candidate miRNAs, only miR-128-3p was both biologically (relative quantity < 30% control or remission patients) and statistically (p<0.01) decreased in the cells during active stage of the disease. This miRNA correlated with a clinical score of the disease well. A set of 10 transcripts involved in the mechanism of the disease was quantified from the same neutrophils RNA. Relative expression of MMP9 was higher in neutrophils from the patients with active disease and correlated negatively with miR-128-3p. The opposite finding was present for MTA1 transcripts. Despite surprisingly scarce changes in the expression of neutrophil miRNAs, miR-128-3p is the best candidate for deciphering etiology of granulomatosis with polyangiitis. |
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AbstractList | Granulomatosis with polyangiitis is a rare chronic inflammatory disease. In this multisystem autoimmune disorder neutrophils cause small vessels necrosis and infiltrate perivascular tissue to form granulomas. Progression of the disease is evaluated by the symptoms score and by a titer of anti-neutrophil cytoplasm antibodies. Despite glucocorticoid and immunosuppressive therapy, prognosis is complicated by chronic renal insufficiency, hearing loss and skin ulceration. In this preliminary study we tested the hypothesis that altered neutrophil expression of miRNAs can contribute to the cell activation, extracellular traps formation and decreased apoptosis. First we compared a profile of 728 miRNAs expressed in circulating neutrophils of patients with active disease and matched healthy donors. Subsequently, candidate miRNAs were quantified in neutrophils from 16 subjects with active disease, 16 asymptomatic patients at the remission and in 16 healthy controls. Out of 11 candidate miRNAs, only miR-128-3p was both biologically (relative quantity < 30% control or remission patients) and statistically (p<0.01) decreased in the cells during active stage of the disease. This miRNA correlated with a clinical score of the disease well. A set of 10 transcripts involved in the mechanism of the disease was quantified from the same neutrophils RNA. Relative expression of MMP9 was higher in neutrophils from the patients with active disease and correlated negatively with miR-128-3p. The opposite finding was present for MTA1 transcripts. Despite surprisingly scarce changes in the expression of neutrophil miRNAs, miR-128-3p is the best candidate for deciphering etiology of granulomatosis with polyangiitis. |
Author | Surmiak, Marcin Hubalewska-Mazgaj, Magdalena Musiał, Jacek Sanak, Marek Wawrzycka-Adamczyk, Katarzyna |
AuthorAffiliation | Department of Internal Medicine Jagiellonian University Medical CollegeKrakow, Poland |
AuthorAffiliation_xml | – name: Department of Internal Medicine Jagiellonian University Medical CollegeKrakow, Poland |
Author_xml | – sequence: 1 givenname: Marcin surname: Surmiak fullname: Surmiak, Marcin organization: Department of Internal Medicine Jagiellonian University Medical CollegeKrakow, Poland – sequence: 2 givenname: Magdalena surname: Hubalewska-Mazgaj fullname: Hubalewska-Mazgaj, Magdalena organization: Department of Internal Medicine Jagiellonian University Medical CollegeKrakow, Poland – sequence: 3 givenname: Katarzyna surname: Wawrzycka-Adamczyk fullname: Wawrzycka-Adamczyk, Katarzyna organization: Department of Internal Medicine Jagiellonian University Medical CollegeKrakow, Poland – sequence: 4 givenname: Jacek surname: Musiał fullname: Musiał, Jacek organization: Department of Internal Medicine Jagiellonian University Medical CollegeKrakow, Poland – sequence: 5 givenname: Marek surname: Sanak fullname: Sanak, Marek organization: Department of Internal Medicine Jagiellonian University Medical CollegeKrakow, Poland |
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Copyright | 2015 Bentham Science Publishers 2015 Marek Sanak |
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Keywords | Granulomatosis with polyangiitis miRNA expression MTA1 Neutrophil TNF-α MMP9 |
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Title | Neutrophil MiRNA-128-3p is Decreased During Active Phase of Granulo-matosis with Polyangiitis |
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