DJ-X-013 ameliorates inflammation by reducing TNF-α/NF-κB expression and experimental colitis by inducing myeloid-derived suppressor cells

نویسندگان

چکیده

Abstract Inflammation is a body’s defense response for short duration however if persists long periods, it causes tissue damage and pathological consequences. Moreover, paves the way several diseases including inflammatory bowel disease (IBD). Therefore, there an urgent need natural safe anti-inflammatory therapeutic compound. To address this issue, we aimed to determine effects of DJ-X-013, using lipopolysaccharide (LPS) activated RAW 264.7 macrophage in vitro dextran sodium sulfate (DSS) induced experimental model colitis vivo. DJ-X-013 drastically reduced tumor necrosis factor-alpha inducible nitric oxide synthase expression LPS-activated macrophages. Further, also impeded NF-κB other markers pathways like IL-6, IL-1β, STAT3, ERK, JNK as compared cells. Additionally, modulates migratory activity macrophages during wound healing. Next, DSS model, observed that reduction body weight colon length were slightly improved group control. Intriguingly, myeloid-derived suppressor cells, neutrophils, CD8 +T cells increased, while Th17 frequency decreased spleen, mesenteric lymph nodes, lamina propria treated DSS. However, killer T marginally enhanced alone. Hence, exhibits immunomodulatory effect might be promising drug IBD diseases, however, further investigation required prudent conclusions. This research supported by NIH grant R01 AI140405

برای دانلود باید عضویت طلایی داشته باشید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Altered gp130 signalling ameliorates experimental colitis via myeloid cell-specific STAT3 activation and myeloid-derived suppressor cells

STAT3 regulates the expansion of myeloid-derived suppressor cells (MDSCs) during inflammation, infection and cancer. Hyperactivation of STAT3 in gp130(757F/F) mice is associated with protection from experimental colitis. This study determined mechanisms for this protection and compared this to mice with myeloid-specific STAT3-deficiency (LysMcre/STAT3(flox); gp130(757F/F) LysMcre/STAT3(flox)). ...

متن کامل

Regulatory T Cells and Myeloid-Derived Suppressor Cells in Patients with Peptic Ulcer and Gastric Cancer

Background: Regulatory T Cells (Tregs) and Myeloid-Derived Suppressor Cells (MDSCs) are two main regulatory cells modulating the immune responses in inflammation and cancer. Objective: To investigate and compare Tregs and MDSCs in peptic ulcer and gastric cancer. Methods: Patients with dyspepsia were selected and divided into three groups of non-ulcer dyspepsia (NUD, n=22), peptic ulcer disease...

متن کامل

Protein Tyrosine Phosphatase 1B Deficiency Ameliorates Murine Experimental Colitis via the Expansion of Myeloid-Derived Suppressor Cells

Protein tyrosine phosphatase 1B (PTP1B) is a key molecule in modulating low-degree inflammatory conditions such as diabetes. The role of PTP1B in other chronic inflammations, however, remains unknown. Here, we report that PTP1B deficiency ameliorates Dextran Sulfate Sodium (DSS)-induced murine experimental colitis via expanding CD11b(+)Gr-1(+) myeloid-derived suppressor cells (MDSCs). Employing...

متن کامل

Myeloid-Derived Suppressor Cells Are Controlled by Regulatory T Cells via TGF-β during Murine Colitis.

Myeloid-derived suppressor cells (MDSCs) are well known regulators of regulatory T cells (Treg cells); however, the direct regulation of MDSCs by Treg cells has not been well characterized. We find that colitis caused by functional deficiency of Treg cells leads to altered expansion and reduced function of MDSCs. During differentiation of MDSCs in vitro from bone marrow cells, Treg cells enhanc...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

ژورنال

عنوان ژورنال: Journal of Immunology

سال: 2023

ISSN: ['1550-6606', '0022-1767']

DOI: https://doi.org/10.4049/jimmunol.210.supp.61.06