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Monosodium urate crystals induced ICAM-1 expression and cell-cell adhesion in renal mesangial cells: Implications for the pathogenesis of gouty nephropathy.
Luo, Shue-Fen; Chin, Chia-Yin; Ho, Ling-Jun; Tseng, Wen-Yi; Kuo, Chang-Fu; Lai, Jenn-Haung.
Afiliação
  • Luo SF; Department of Rheumatology, Allergy and Immunology, Chang Gung Memorial Hospital (at Lin-Kou), Tao-Yuan, Taiwan, ROC; Department of Medicine, Chang Gung University, Tao-Yuan, Taiwan, ROC. Electronic address: lsf00076@adm.cgmh.org.tw.
  • Chin CY; Department of Rheumatology, Allergy and Immunology, Chang Gung Memorial Hospital (at Lin-Kou), Tao-Yuan, Taiwan, ROC.
  • Ho LJ; Institute of Cellular and System Medicine, National Health Research Institute, Zhunan, Taiwan, ROC.
  • Tseng WY; Department of Rheumatology, Allergy and Immunology, Chang Gung Memorial Hospital (at Keelung), Keelung, Taiwan, ROC.
  • Kuo CF; Department of Rheumatology, Allergy and Immunology, Chang Gung Memorial Hospital (at Lin-Kou), Tao-Yuan, Taiwan, ROC.
  • Lai JH; Department of Rheumatology, Allergy and Immunology, Chang Gung Memorial Hospital (at Lin-Kou), Tao-Yuan, Taiwan, ROC; Graduate Institute of Medical Science, National Defense Medical Center, Taipei, Taiwan, ROC. Electronic address: laiandho@gmail.com.
J Microbiol Immunol Infect ; 53(1): 23-32, 2020 Feb.
Article em En | MEDLINE | ID: mdl-29657028
BACKGROUND: Renal disease is prevalent in gouty patients and monosodium urate (MSU) crystal deposition in the kidney can be detected in some gouty nephropathy patients. MSU crystals can induce inflammatory events, we investigated the MSU-induced expression of intercellular adhesion molecule (ICAM)-1 on human renal mesangial cells (HRMCs) and the involved signal transduction mechanisms. METHODS: The HRMCs cell line was purchased from ScienCell Research Laboratories. MSU crystals were made by dissolving uric acid in sodium hydroxide (NaOH) solution. The involvement of MAPKs, apoptosis-associated speck-like protein containing a CARD domain (ASC), and Toll-like receptor (TLR) was investigated using pharmacological inhibitors, transfection with short hairpin RNA (shRNA), or monoclonal antibodies. Protein expression was evaluated by Western blotting. The functional activity of ICAM-1 was evaluated with cell-cell adhesion assay and immunofluorescence analysis. RESULTS: MSU stimulation increased expression of ICAM-1 and adhesion between HRMCs and human monocytic THP-1 cells. The interaction between HRMCs and THP-1 was suppressed by ICAM-1 neutralizing antibodies. MSU stimulation induced activation of mitogen-activated protein kinases, including c-Jun N-terminal kinase (JNK), p38, and extracellular signal-regulated kinase (ERK), but only p38 was responsible for MSU-induced expression of ICAM-1 and cell-cell adhesion. ASC also play a role in MSU-induced effects. Pretreatment with monoclonal antibodies against toll-like receptor (TLR)2 or TLR4 reduced MSU-induced ICAM-1 expression, cell-cell adhesion, p38 phosphorylation but the reduction of ASC activation is insignificant. CONCLUSION: The MSU induced ICAM-1 expression on HRMCs and cell-cell adhesion involved TLR2/4-p38-ICAM1 pathway and TLR2/4 independent ASC-p38-ICAM1 axis. These findings might partly explain the mechanisms underlying gouty nephropathy.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Ácido Úrico / Adesão Celular / Molécula 1 de Adesão Intercelular / Células Mesangiais / Gota / Nefropatias Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Ácido Úrico / Adesão Celular / Molécula 1 de Adesão Intercelular / Células Mesangiais / Gota / Nefropatias Idioma: En Ano de publicação: 2020 Tipo de documento: Article