Fengling Li
University of Pittsburgh
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Publication
Featured researches published by Fengling Li.
Journal of Biological Chemistry | 2003
Chen Zhu; Kavitha N. Rao; Huabao Xiong; Khatuna Gagnidze; Fengling Li; Curt M. Horvath; Scott E. Plevy
Interleukin (IL)-12 is a heterodimeric cytokine that is critical for the development of a T-helper-1 immune response and immunity against intracellular pathogens. The IL-12 p40 gene product, expressed specifically in macrophages and dendritic cells, heterodimerizes with p35 to form bioactive IL-12, and heterodimerizes with p19 to comprise the cytokine IL-23. Regulation of the murine IL-12 p40 promoter is complex. Multiple cis-acting elements have been characterized that are involved in activation by bacterial products. However, molecular mechanisms through which interferon (IFN)-γ and bacterial products synergistically activate IL-12 p40 gene expression are less clear. In this study, a composite NFAT/ICSBP binding site at –68 to –54 is identified that is functionally important for p40 promoter activation by lipopolysaccharide (LPS) and LPS plus IFN-γ. DNA binding of NFAT and ICSBP is demonstrated on the endogenous promoter by chromatin immunoprecipitation. NFAT is required for ICSBP binding to this region. Overexpression of NFAT and ICSBP synergistically activates the p40 promoter. A dominant negative NFAT molecule attenuates LPS- and IFN-γ-activated endogenous IL-12 p40 mRNA expression. A physical association between NFAT and ICSBP in the absence of DNA is detected by co-immunoprecipitation of endogenous proteins. Three NFAT domains are required for ICSBP interaction. Finally, in LPS- and IFN-γ-activated RAW-264.7 cells, the association between NFAT and ICSBP is abrogated by IL-10 priming.
Gastroenterology | 2009
Shehzad Z. Sheikh; Katsuyoshi Matsuoka; Jennifer K. Uno; Fengling Li; Scott E. Plevy
Background: Interleukin (IL)-12 and 23 are heterodimeric cytokines composed of a common p40 subunit and p35 and p19 subunits, respectively. IL-23 is strongly implicated in the pathogenesis of inflammatory bowel disease. Aim: The aim of this study is to characterize the molecular regulation of Il23a gene expression and promoter activation in murine macrophages and experimental colitis. Results: Interferon-γ (IFN-γ) inhibits LPS-induced Il23a mRNA and IL-23 protein expression in murine bone marrow-derived macrophages (BMMs). A conserved nucleotide sequence across multiple species was identified in the promoter of the Il23a gene that contains an interferon stimulated response element (ISRE). In LPS and IFN-γ activated BMMs, chromatin immunoprecipitation and electrophoretic mobility shift assays demonstrate that interferon regulatory factors (IRFs) interact with this ISRE. Using a 1.8 kb murine Il23a luciferase reporter plasmid, LPS induces and IFN-γ inhibits LPSinduced p19 promoter activity in BMMs. Mutations in the ISRE abrogate IFN-γ inhibition of LPS-induced promoter activity. To understand the contribution of specific IRFs, IRF-1 was inhibited in BMMs by siRNA and experiments were performed in IRF-1 deficient (-/-) macrophages. IRF-1 knockdown and IRF-1-/BMMs demonstrate increased LPS-induced IL-23 expression. Primary response genes have promoters that either exist in an open chromatin structure or undergo rapid nucleosomal remodeling. In contrast, secondary response genes with delayed induction kinetics require new protein synthesis prior to transcription initiation. Il23a expression in LPS-activated BMMs demonstrates rapid induction kinetics and unlike Il12b (established secondary response gene) is not dependent on new protein synthesis. Interestingly, LPS plus IFN-γ activated BMMs demonstrate loss of the IFN-γ inhibitory effect, suggesting IFN-γ mediated regulation of Il23a requires new protein synthesis. Il23a regulation was then studied in murine colitis models. Following intrarectal administration of TNBS, IRF-1-/mice exhibit increased inflammation and increased colonic IL-23 expression compared to wild type (WT) mice. Additionally, we demonstrate mucosal regulation of IL-23 by the enteric microbiota using germ-free and conventionalized WT and colitis-prone IL-10-/mice. Enteric bacteria induce significantly higher intestinal IL-23 expression in IL-10-/-mice compared withWTmice. Conclusions: IFN-γ and IRF-1 negatively regulate Il23a in murine macrophages and experimental colitis. Regulation of intestinal Il23a by the enteric microflora is a significant event in the initiation of chronic intestinal inflammation.
Journal of Biological Chemistry | 2004
Huabao Xiong; Chen Zhu; Fengling Li; Refaat Hegazi; Kaili He; Mark Babyatsky; Anthony J. Bauer; Scott E. Plevy
Archive | 2017
Fengling Li; Tara C. Rubinas; Scott E. Plevy; Shehzad Z. Sheikh; Katsuyoshi Matsuoka; Taku Kobayashi
Archive | 2013
Yingzhang Lin; R. Balfour Sartor; Robert W; Hemant K. Parekh; Satya P. Kunapuli; Fengling Li; Anthony Stadnicki
The FASEB Journal | 2010
Jennifer K. Uno; Katsuyoshi Matsuoka; Shehzad Z. Sheikh; Houda Zghal Elloumi; Fengling Li; Scott E. Plevy
Gastroenterology | 2010
Jennifer K. Uno; Katsuyoshi Matsuoka; Shehzad Z. Sheikh; Fengling Li; Erin C. Steinbach; Steven Russo; R. Balfour Sartor; Scott E. Plevy
Gastroenterology | 2009
Jennifer K. Uno; Kavitha N. Rao; Katsuyoshi Matsuoka; Shehzad Z. Sheikh; Fengling Li; Scott E. Plevy
Gastroenterology | 2009
Shehzad Z. Sheikh; Katsuyoshi Matsuoka; Jennifer K. Uno; Fengling Li; Scott E. Plevy
Gastroenterology | 2009
Katsuyoshi Matsuoka; Shehzad Z. Sheikh; Fengling Li; Jennifer K. Uno; Scott E. Plevy