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Increased FURIN expression in rheumatoid arthritis patients and its anti‐inflammatory effect

BACKGROUND: FURIN belongs to the proprotein convertase family that processes proproteins and is involved in many diseases. However, the role of FURIN in rheumatoid arthritis (RA) remains unknown. In this study, we investigated the association between circulating FURIN and disease activity in patient...

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Autores principales: Cao, Rong, Zhang, Ying, Du, Juping, Chen, Shuaishuai, Wang, Na, Ying, Haijian, Shen, Bo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7755791/
https://www.ncbi.nlm.nih.gov/pubmed/32840921
http://dx.doi.org/10.1002/jcla.23530
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author Cao, Rong
Zhang, Ying
Du, Juping
Chen, Shuaishuai
Wang, Na
Ying, Haijian
Shen, Bo
author_facet Cao, Rong
Zhang, Ying
Du, Juping
Chen, Shuaishuai
Wang, Na
Ying, Haijian
Shen, Bo
author_sort Cao, Rong
collection PubMed
description BACKGROUND: FURIN belongs to the proprotein convertase family that processes proproteins and is involved in many diseases. However, the role of FURIN in rheumatoid arthritis (RA) remains unknown. In this study, we investigated the association between circulating FURIN and disease activity in patients with RA and the effect of FURIN in THP‐1‐derived macrophages. METHODS: A total of 108 RA patients and 39 healthy controls participants were included in this study. RA patients were divided into four disease activity groups determined by the Disease Activity Score of 28 joints (DAS28). FURIN expression in peripheral blood mononuclear cells (PBMCs) and serum was detected by using quantitative real‐time polymerase chain reaction (qRT‐PCR) and enzyme‐linked immunosorbent assay (ELISA), respectively. Western blotting and qRT‐PCR were used to detect cytokines level after interfering FURIN expressed in THP‐1‐derived macrophages. RESULTS: Both FURIN mRNA and protein levels were significantly higher in RA patients than in healthy controls participants (P < .001). No significant difference in FURIN expression was observed among the four RA groups (P > .05). Spearman correlation revealed that FURIN positively correlated with transforming growth factor‐β1(TGF‐β1), rheumatoid factor (RF), and anti‐cyclic citrullinated peptide (anti‐CCP). Moreover, the inhibition of FURIN in THP‐1‐derived macrophages promoted the caspase‐1 and IL‐1β expression (P < .05). CONCLUSION: FURIN levels were significantly increased in the peripheral blood of RA patients and were not associated with disease activity. The inhibition of FURIN in THP‐1‐derived macrophages with elevated IL‐1β levels shows that FURIN may have an anti‐inflammatory effect.
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spelling pubmed-77557912020-12-23 Increased FURIN expression in rheumatoid arthritis patients and its anti‐inflammatory effect Cao, Rong Zhang, Ying Du, Juping Chen, Shuaishuai Wang, Na Ying, Haijian Shen, Bo J Clin Lab Anal Research Articles BACKGROUND: FURIN belongs to the proprotein convertase family that processes proproteins and is involved in many diseases. However, the role of FURIN in rheumatoid arthritis (RA) remains unknown. In this study, we investigated the association between circulating FURIN and disease activity in patients with RA and the effect of FURIN in THP‐1‐derived macrophages. METHODS: A total of 108 RA patients and 39 healthy controls participants were included in this study. RA patients were divided into four disease activity groups determined by the Disease Activity Score of 28 joints (DAS28). FURIN expression in peripheral blood mononuclear cells (PBMCs) and serum was detected by using quantitative real‐time polymerase chain reaction (qRT‐PCR) and enzyme‐linked immunosorbent assay (ELISA), respectively. Western blotting and qRT‐PCR were used to detect cytokines level after interfering FURIN expressed in THP‐1‐derived macrophages. RESULTS: Both FURIN mRNA and protein levels were significantly higher in RA patients than in healthy controls participants (P < .001). No significant difference in FURIN expression was observed among the four RA groups (P > .05). Spearman correlation revealed that FURIN positively correlated with transforming growth factor‐β1(TGF‐β1), rheumatoid factor (RF), and anti‐cyclic citrullinated peptide (anti‐CCP). Moreover, the inhibition of FURIN in THP‐1‐derived macrophages promoted the caspase‐1 and IL‐1β expression (P < .05). CONCLUSION: FURIN levels were significantly increased in the peripheral blood of RA patients and were not associated with disease activity. The inhibition of FURIN in THP‐1‐derived macrophages with elevated IL‐1β levels shows that FURIN may have an anti‐inflammatory effect. John Wiley and Sons Inc. 2020-08-25 /pmc/articles/PMC7755791/ /pubmed/32840921 http://dx.doi.org/10.1002/jcla.23530 Text en © 2020 The Authors. Journal of Clinical Laboratory Analysis published by Wiley Periodicals LLC This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Cao, Rong
Zhang, Ying
Du, Juping
Chen, Shuaishuai
Wang, Na
Ying, Haijian
Shen, Bo
Increased FURIN expression in rheumatoid arthritis patients and its anti‐inflammatory effect
title Increased FURIN expression in rheumatoid arthritis patients and its anti‐inflammatory effect
title_full Increased FURIN expression in rheumatoid arthritis patients and its anti‐inflammatory effect
title_fullStr Increased FURIN expression in rheumatoid arthritis patients and its anti‐inflammatory effect
title_full_unstemmed Increased FURIN expression in rheumatoid arthritis patients and its anti‐inflammatory effect
title_short Increased FURIN expression in rheumatoid arthritis patients and its anti‐inflammatory effect
title_sort increased furin expression in rheumatoid arthritis patients and its anti‐inflammatory effect
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7755791/
https://www.ncbi.nlm.nih.gov/pubmed/32840921
http://dx.doi.org/10.1002/jcla.23530
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