Introduction and Aims: Micro RNAs (miR) are molecules of 20-30 non-coding nucleotides regulating a multitude of biological processes. MiR-155 is a recognized biomarker of several B-cell lymphomas, and recent experimental works have associated miR-155 up-regulation with an increase of inflammatory response. This study aimed to analyze, a) basal expression of miR-155 in peripheral blood mononuclear cells (PBMC) of chronic hemodialysis (HD) patients, and b) PBMC miR-155 expression during human blood contact to low permeability polysulphone hemodialysis membranes before (long interval period) and after standard 4-hour HD sessions. Methods: PBMC miR-155 was isolated from 7 healthy laboratory individuals (CTRLs; (age 30-50 years; 3F, 4M) and 9 HD patients (age 50-75 years; 1F, 8M) using miRNeasy mini kit and quantified by real-time PCR. All HD patients were free from hematological, inflammatory or neoplastic diseases. Data are expressed as mean; ± standard error; statistical differences were identified by t-test. Results: MiR-155 relative (to CTRLs) quantity (RQ) from long period pre-HD was 3.77; ± 0.62 times higher than CTRLs (P = 0.003). No differences were instead observed after HD sessions, 3.49; ± 0.70 RQ (P = NS vs. pre-HD). Conclusions: These preliminary data from HD PBMC show a significant up-regulation of miR-155 when compared to CTRLs. It also looks that interaction of PBMC to low permeability polysulphone membranes doesn’t increase monocyte miR-155 basal up-regulation. Further studies will be carried out to clarify the role of HD and renal failure for miR-155 expression.

PBMC microRNA-155 is up-regulated in chronic hemodialysis patients.

GNECCHI, MASSIMILIANO;CERVIO, ELISABETTA;Rampino T;LIBETTA, CARMELO;
2012-01-01

Abstract

Introduction and Aims: Micro RNAs (miR) are molecules of 20-30 non-coding nucleotides regulating a multitude of biological processes. MiR-155 is a recognized biomarker of several B-cell lymphomas, and recent experimental works have associated miR-155 up-regulation with an increase of inflammatory response. This study aimed to analyze, a) basal expression of miR-155 in peripheral blood mononuclear cells (PBMC) of chronic hemodialysis (HD) patients, and b) PBMC miR-155 expression during human blood contact to low permeability polysulphone hemodialysis membranes before (long interval period) and after standard 4-hour HD sessions. Methods: PBMC miR-155 was isolated from 7 healthy laboratory individuals (CTRLs; (age 30-50 years; 3F, 4M) and 9 HD patients (age 50-75 years; 1F, 8M) using miRNeasy mini kit and quantified by real-time PCR. All HD patients were free from hematological, inflammatory or neoplastic diseases. Data are expressed as mean; ± standard error; statistical differences were identified by t-test. Results: MiR-155 relative (to CTRLs) quantity (RQ) from long period pre-HD was 3.77; ± 0.62 times higher than CTRLs (P = 0.003). No differences were instead observed after HD sessions, 3.49; ± 0.70 RQ (P = NS vs. pre-HD). Conclusions: These preliminary data from HD PBMC show a significant up-regulation of miR-155 when compared to CTRLs. It also looks that interaction of PBMC to low permeability polysulphone membranes doesn’t increase monocyte miR-155 basal up-regulation. Further studies will be carried out to clarify the role of HD and renal failure for miR-155 expression.
2012
Nephrology Dialysis Transplantation
The Urology & Nephrology category covers general urology and nephrology resources, specialty resources on the prostate, dialysis and other blood purification techniques, transplantation and renal failure.
Sì, ma tipo non specificato
Inglese
contributo
49° European Renal Association - European Dialysis and Transplant Association (ERA-EDTA) Congress
24-27 Maggio 2012
Paris (France)
Internazionale
ELETTRONICO
27 Suppl 2 (Abstract SAP280)
ii411
ii411
PERIPHERAL BLOOD MONONUCLEAR CELLS; microRNA; CHRONIC HEMODIALYSIS
none
Sepe, V; Albrizio, P; Gnecchi, Massimiliano; Cervio, Elisabetta; Esposito, P; Rampino, T; Libetta, Carmelo; Dal Canton, A.
273
info:eu-repo/semantics/conferenceObject
8
4 Contributo in Atti di Convegno (Proceeding)::4.1 Contributo in Atti di convegno
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11571/466974
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