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Published on: June 15, 2016
STAT3 Activates the Pentraxin 3 Gene in Chronic Lymphocytic Leukemia Cells
Uri Rozovski1,2,3, Ivo Veletic1, David M Harris1
1Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX.
Insights
Chronic lymphocytic leukemia (CLL) cells produce pentraxin-related protein 3 (PTX3). STAT3 activation drives PTX3 gene transcription in CLL cells, and PTX3 downregulation enhances CLL cell apoptosis, suggesting a therapeutic target.
Area of Science:
- Immunology
- Molecular Biology
- Hematology
Background:
- Pentraxin-related protein 3 (PTX3) is a key innate immune system component.
- Elevated PTX3 plasma levels are observed in patients with chronic lymphocytic leukemia (CLL).
Purpose of the Study:
- To investigate the source and regulation of PTX3 in CLL.
- To explore the functional role of PTX3 in CLL pathogenesis.
Main Methods:
- Western immunoblotting and flow cytometry to detect PTX3 production by CLL cells.
- Confocal microscopy to localize PTX3 within CLL cells.
- Chromatin immunoprecipitation, STAT3 knockdown, EMSA, and dual-luciferase reporter assays to analyze PTX3 gene regulation by STAT3.
Main Results:
- CLL cells, specifically CD19+CD5+ B lymphocytes, were identified as the source of high PTX3 levels.
- Constitutively activated STAT3 in CLL cells directly binds to and transcriptionally activates the PTX3 gene promoter.
- STAT3 knockdown significantly reduced PTX3 expression.
- Downregulation of PTX3 expression promoted apoptosis in CLL cells.
Conclusions:
- CLL cells produce PTX3, driven by STAT3-mediated transcriptional activation.
- PTX3 plays a role in CLL cell survival, as its downregulation induces apoptosis.
- Targeting PTX3 may represent a potential therapeutic strategy for chronic lymphocytic leukemia.
Abstract:
Pentraxin-related protein 3 (PTX3), commonly produced by myeloid and endothelial cells, is a humoral pattern recognition protein of the innate immune system. Because PTX3 plasma levels of patients with chronic lymphocytic leukemia (CLL) are high and most circulating cells in patients with CLL are CLL cells, we reasoned that CLL cells produce PTX3. Western immunoblotting revealed that low-density cells from seven of seven patients with CLL produce high levels of PTX3, flow cytometry analysis revealed that the PTX3-producing cells are B lymphocytes coexpressing CD19 and CD5, and confocal microscopy showed that PTX3 is present in the cytoplasm of CLL cells. Because STAT3 is constitutively activated in CLL cells, and because we identified putative STAT3 binding sites within the PTX3 gene promoter, we postulated that phosphorylated STAT3 triggers transcriptional activation of PTX3. Immunoprecipitation analysis of CLL cells' chromatin fragments showed that STAT3 Abs precipitated PTX3 DNA. STAT3 knockdown induced a marked reduction in PTX3 expression, indicating a STAT3-induced transcriptional activation of the PTX3 gene in CLL cells. Using an EMSA, we established and used a dual-reporter luciferase assay to confirm that STAT3 binds the PTX3 gene promoter. Downregulation of PTX3 enhanced apoptosis of CLL cells, suggesting that inhibition of PTX3 might benefit patients with CLL.
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