Mesangial cells of lupus-prone mice are sensitive to chemokine production

Shuk Man Ka, Chao-Wen Cheng, Hao Ai Shui, Wen Mein Wu, Deh Ming Chang, Yu Chu Lin, Ann Chen

Research output: Contribution to journalArticle

33 Citations (Scopus)

Abstract

Infectious antigens may be triggers for the exacerbation of systemic lupus erythematosus. The underlying mechanism causing acceleration and exacerbation of lupus nephritis (LN) is largely unknown. Bacterial lipopolysaccharide (LPS) is capable of inducing an accelerated model of LN in NZB/W mice, featuring diffuse proliferation of glomerular resident cells. We hypothesized that mesangial cells (MCs) from LN subjects are more responsive to LPS than normal subjects. Cultured primary NZB/W and DBA/W (nonautoimmune disease-prone strain with MHC class II molecules identical to those of NZB/W) MCs were used. Monocyte chemoattractant protein-1 (MCP-1) and osteopontin (OPN) expressions either in the baseline (normal culture) condition or in the presence of LPS were evaluated by real-time PCR, ELISA, or western blot analysis. NF-κB was detected by ELISA, electrophoresis mobility-shift assay, and immunofluorescence. First, either in the baseline condition or in the presence of LPS, NZB/W MCs produced significantly higher levels of MCP-1 and OPN than the DBA/W MC controls. Second, NZB/W MCs expressed significantly higher levels of Toll-like receptor 4, myeloid differentiation factor 88, and NF-κB than the DBA/W MC controls, both receiving exactly the same LPS treatment. In conclusion, NZB/W MCs are significantly more sensitive than their normal control DBA/W MCs in producing both MCP-1 and OPN. With LPS treatment, the significantly elevated levels of both chemokines produced by NZB/W MCs are more likely due to a significantly greater activation of the Toll-like receptor 4-myeloid differentiation factor 88-associated NF-κB pathway. The observed abnormal molecular events provide an intrarenal pathogenic pathway involved in an accelerated type of LN, which is potentially infection triggered.

Original languageEnglish
Article numberR67
JournalArthritis Research and Therapy
Volume9
Issue number4
DOIs
Publication statusPublished - Jul 7 2007
Externally publishedYes

Fingerprint

Mesangial Cells
Chemokines
Lipopolysaccharides
Lupus Nephritis
Osteopontin
Chemokine CCL2
Myeloid Differentiation Factor 88
Toll-Like Receptor 4
Enzyme-Linked Immunosorbent Assay
Inbred NZB Mouse
Electrophoretic Mobility Shift Assay
Systemic Lupus Erythematosus
Fluorescent Antibody Technique
Electrophoresis
Real-Time Polymerase Chain Reaction
Western Blotting
Antigens

ASJC Scopus subject areas

  • Rheumatology
  • Immunology
  • Immunology and Allergy
  • Medicine(all)

Cite this

Mesangial cells of lupus-prone mice are sensitive to chemokine production. / Ka, Shuk Man; Cheng, Chao-Wen; Shui, Hao Ai; Wu, Wen Mein; Chang, Deh Ming; Lin, Yu Chu; Chen, Ann.

In: Arthritis Research and Therapy, Vol. 9, No. 4, R67, 07.07.2007.

Research output: Contribution to journalArticle

Ka, Shuk Man ; Cheng, Chao-Wen ; Shui, Hao Ai ; Wu, Wen Mein ; Chang, Deh Ming ; Lin, Yu Chu ; Chen, Ann. / Mesangial cells of lupus-prone mice are sensitive to chemokine production. In: Arthritis Research and Therapy. 2007 ; Vol. 9, No. 4.
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abstract = "Infectious antigens may be triggers for the exacerbation of systemic lupus erythematosus. The underlying mechanism causing acceleration and exacerbation of lupus nephritis (LN) is largely unknown. Bacterial lipopolysaccharide (LPS) is capable of inducing an accelerated model of LN in NZB/W mice, featuring diffuse proliferation of glomerular resident cells. We hypothesized that mesangial cells (MCs) from LN subjects are more responsive to LPS than normal subjects. Cultured primary NZB/W and DBA/W (nonautoimmune disease-prone strain with MHC class II molecules identical to those of NZB/W) MCs were used. Monocyte chemoattractant protein-1 (MCP-1) and osteopontin (OPN) expressions either in the baseline (normal culture) condition or in the presence of LPS were evaluated by real-time PCR, ELISA, or western blot analysis. NF-κB was detected by ELISA, electrophoresis mobility-shift assay, and immunofluorescence. First, either in the baseline condition or in the presence of LPS, NZB/W MCs produced significantly higher levels of MCP-1 and OPN than the DBA/W MC controls. Second, NZB/W MCs expressed significantly higher levels of Toll-like receptor 4, myeloid differentiation factor 88, and NF-κB than the DBA/W MC controls, both receiving exactly the same LPS treatment. In conclusion, NZB/W MCs are significantly more sensitive than their normal control DBA/W MCs in producing both MCP-1 and OPN. With LPS treatment, the significantly elevated levels of both chemokines produced by NZB/W MCs are more likely due to a significantly greater activation of the Toll-like receptor 4-myeloid differentiation factor 88-associated NF-κB pathway. The observed abnormal molecular events provide an intrarenal pathogenic pathway involved in an accelerated type of LN, which is potentially infection triggered.",
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