Antitumor Macrophage Response to Bacillus pumilus Ribonuclease (Binase)

Autor: Klaus T. Preissner, Julian Rodriguez-Montesinos, Alexander Nesmelov, A. V. Makeeva, Hector A. Cabrera-Fuentes, Pavel V. Zelenikhin, Olga N. Ilinskaya
Rok vydání: 2017
Předmět:
0301 basic medicine
toll like receptor adaptor molecule 1
animal cell
immune response
0302 clinical medicine
Bacillus pumilus ribonuclease
Bacillus pumilus
Toll-like receptor
biology
toll like receptor
unclassified drug
cytokine release
030220 oncology & carcinogenesis
THP-1 cell line
Tumor necrosis factor alpha
ribonuclease
monocyte chemotactic protein 1
lcsh:RB1-214
Article Subject
tumor necrosis factor
Immunology
transcription factor RelA
interleukin 6
macrophage
malignant neoplasm
interleukin 4
Article
03 medical and health sciences
lcsh:Pathology
controlled study
human
Ribonuclease
protein expression
mouse
Interleukin 4
A549 cell
polarization
nonhuman
bacterial enzyme
myeloid differentiation factor 88
human cell
RNA
RAW 264.7 cell line
Cell Biology
biology.organism_classification
Molecular biology
030104 developmental biology
7 INGENIERÍA Y TECNOLOGÍA
TRIF
biology.protein
interleukin 10
Zdroj: Mediators of Inflammation, Vol 2017 (2017)
Mediators of Inflammation
ISSN: 1466-1861
0962-9351
DOI: 10.1155/2017/4029641
Popis: Extracellular bacterial ribonucleases such as binase from Bacillus pumilus possess cytotoxic activity against tumor cells with a potential for clinical application. Moreover, they may induce activation of tumor-derived macrophages either into the M1-phenotype with well-documented functions in the regulation of the antitumor immune response or into M2-macrophages that may stimulate tumor growth, metastasis, and angiogenesis. In this study, binase or endogenous RNase1 (but not RNA or short oligonucleotides) stimulated the expression of activated NF-κB p65 subunit in macrophages. Since no changes in MyD88 and TRIF adaptor protein expression were observed, toll-like receptors may not be involved in RNase-related NF-κB pathway activation. In addition, short exposure (0.5 hr) to binase induced the release of cytokines such as IL-6, МСР-1, or TNF-α (but not IL-4 and IL-10), indicative for the polarization into antitumor M1-macrophages. Thus, we revealed increased expression of activated NF-κB p65 subunit in macrophages upon stimulation by binase and RNase1, but not RNA or short oligonucleotides.
Databáze: OpenAIRE