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Updated: Jun 12, 2026

Monitoring Neutrophil Elastase and Cathepsin G Activity in Human Sputum Samples
Published on: May 21, 2021
Elevated neutrophil membrane expression of proteinase 3 is dependent upon CD177 expression
M Abdgawad1, L Gunnarsson, A A Bengtsson
1Department of Nephrology, Lund University, Lund, Sweden. Mohamed.Abdgawad@med.lu.se
Abstract:
Proteinase 3 (PR3) is a major autoantigen in anti-neutrophil cytoplasmic antibodies (ANCA)-associated systemic vasculitis (AASV), and the proportion of neutrophils expressing PR3 on their membrane (mPR3+) is increased in AASV. We have shown recently that mPR3 and CD177 are expressed on the same cells in healthy individuals. In this study we try to elucidate mechanisms behind the increased mPR3 expression in AASV and its relationship to CD177. All neutrophils in all individuals were either double-positive or double-negative for mPR3 and CD177. The proportion of double-positive neutrophils was increased significantly in AASV and systemic lupus erythematosus patients. The proportion of mPR3+/CD177+ cells was not correlated to general inflammation, renal function, age, sex, drug treatment and levels of circulating PR3. AASV patients had normal levels of granulocyte colony-stimulating factor and granulocyte-macrophage colony-stimulating factor. Pro-PR3 was found to constitute 10% of circulating PR3 but none of the mPR3. We found increased mRNA levels of both PR3 and CD177 in AASV, but they did not correlate with the proportion of double-positive cells. In cells sorted based on membrane expression, CD177-mRNA was several-fold higher in mPR3+ cells. When exogenous PR3 was added to CD177-transfected U937 cells, only CD177+ cells bound PR3 to their membrane. In conclusion, the increased membrane expression of PR3 found in AASV is not linked directly to circulating PR3 or PR3 gene transcription, but is dependent upon CD177 expression and correlated with the transcription of the CD177 gene.
Insights
Increased membrane-bound Proteinase 3 (mPR3) in anti-neutrophil cytoplasmic antibodies (ANCA)-associated systemic vasculitis (AASV) is linked to CD177 expression, not PR3 levels. This suggests CD177 drives mPR3 expression in AASV.
Area of Science:
- Immunology
- Cell Biology
- Autoimmune Diseases
Background:
- Proteinase 3 (PR3) is a key autoantigen in ANCA-associated systemic vasculitis (AASV).
- Increased membrane-bound PR3 (mPR3) on neutrophils is observed in AASV patients.
- Previous work indicated co-expression of mPR3 and CD177 on neutrophils in healthy individuals.
Purpose of the Study:
- To investigate the mechanisms behind elevated mPR3 expression in AASV.
- To clarify the relationship between mPR3 and CD177 in AASV pathogenesis.
- To determine factors influencing mPR3 and CD177 co-expression.
Main Methods:
- Flow cytometry to analyze mPR3 and CD177 expression on neutrophils.
- Correlation analysis with clinical parameters (inflammation, renal function, demographics, treatment).
- Measurement of PR3 and CD177 mRNA levels.
- In vitro experiments using CD177-transfected U937 cells and exogenous PR3.
Main Results:
- Neutrophils were either double-positive or double-negative for mPR3 and CD177.
- The proportion of mPR3+/CD177+ neutrophils was significantly elevated in AASV and systemic lupus erythematosus patients.
- mPR3 expression was dependent on CD177 expression and correlated with CD177 gene transcription, not PR3 levels or transcription.
Conclusions:
- Increased mPR3 in AASV is primarily driven by CD177 expression, not by circulating PR3 or PR3 gene transcription.
- CD177 plays a crucial role in mediating the membrane binding of PR3 in AASV.
- The findings highlight a CD177-dependent mechanism for enhanced PR3 presentation on neutrophils in AASV.

