MyD88 associated ROS generation is crucial for lactobacillus induced IL-12 production in macrophage

29Citations
Citations of this article
35Readers
Mendeley users who have this article in their library.

Abstract

It is well known that some strains of lactic acid bacteria (LAB) can induce IL-12 which plays an important role in modulating immune responses. However, the mechanisms by which LAB induce IL-12 production remain unclear. Here, we examine the role of toll-like receptors (TLR's) and reactive oxygen species (ROS) in IL-12 production by LAB stimulated peritoneal macrophages. Our results indicate that a TLR is not necessary for IL-12 induction by LAB, whilst the universal adaptor protein, MyD88, is essential. Specific strains of LAB induced ROS that correlated with both the frequency of phagocytosis and IL-12 production. Reduction in IL-12 production by NADPH oxidase inhibitors or ROS scavengers demonstrates the crucial role of ROS in IL-12 induction. Interestingly, deficiency of TLR2, 4, 9 or MyD88 did not affect the phagocytosis of LAB strain KW3110, a potent IL-12 inducer, and ROS production was significantly reduced only in MyD88 deficient macrophages. These results suggest the existence of TLR-MyD88 independent LAB recognition and MyD88 related ROS induction mechanisms. We show here the importance of ROS for IL-12 induction and provide new insights into IL-12 induction by LAB. © 2012 Ichikawa et al.

Figures

  • Figure 1. IL-12 production by macrophage correlates with the frequency of LAB phagocytosis and ROS production. (A, B) Peritoneal macrophages were cultured with FITC-labeled identical LAB strains (3 mg/ml) in a chamber slide. Following the culture for 8 hrs, macrophages were stained with CD11b antibody (red) and phagocytosis of LAB (green) was analyzed by confocal microscopy. Representative pictures (A) and mean phagocytosis index 6 SD (B) are shown. (C) Peritoneal macrophages were cultured with 1 mg/ml LAB strains for 24 hr and the levels of IL-12p70 in the culture supernatants were determined by ELISA. (D) Peritoneal macrophages were cultured with 1 mg/ml KW3110, ATCC53103 or NRIC1942 for 8 hrs. ROS were measured using the luminescent dye L-012 at the end of culture. (E) Peritoneal macrophages were cultured with KW3110 (filled) or ATCC53103 (blank) with apocynin (0, 0.1, 0.5, 2 mM) and ROS production measured similarly. Values are average of duplicated culture except figure 1B. Representative data from more than three independent experiments yielding consistent results are shown. doi:10.1371/journal.pone.0035880.g001
  • Table 1. IL-12 and ROS production from macrophages stimulated by various strains of LAB.
  • Figure 2. Kinetic analysis of ROS production, IL-12 mRNA expression and IL-12 production from macrophage after LAB stimulation. Peritoneal macrophages were cultured with 1 mg/ml KW3110 and IL-12p35 and IL-12p40 mRNA expression (A), IL-12p40 and IL-12p70 production (B) and ROS production (C) were measured over time. Values are mean of duplicate culture (C) or mean 6 SD of triplicate culture (A, B). Data are representative of three independent experiments yielding similar results. doi:10.1371/journal.pone.0035880.g002
  • Figure 3. ROS dependent IL-12 production from LAB stimulated macrophage. (A) Peritoneal macrophages were cultured with 1 mg/ml KW3110, ATCC53103 or 1 mM CpG for 24 hrs in the presence of 0, 0.1, 0.5 or 2 mM apocynin (Apo) or 0, 0.01, 0.05 or 0.2 mM propyl gallate (PG). IL12p40 and IL-12p70 in the cell culture supernatant were measured by ELISA. (C) Peritoneal macrophages were cultured with FITC-labeled identical KW3110 (3 mg/ml) in the presence of Apocynin or propyl gallate. Phagocytosis index was calculated in the same manner as described in Fig. 1A. Data are representative of three independent experiments. doi:10.1371/journal.pone.0035880.g003
  • Figure 4. MyD88 dependent but TLR independent IL-12 production from peritoneal macrophages stimulated by LAB.
  • Figure 5. MyD88-deficient macrophage shows impaired ROS production. (A) Peritoneal macrophages were prepared from wild type and TLR2-, 4-, 9- and MyD88-deficient mice. Cells were cultured with FITC-labeled KW3110 (3 mg/ml) in a chamber slide and phagocytosis indices were measured as described in Fig. 1B. Data value is the mean 6 SD of three mice. (B) Macrophage from wild type and TLR2-, 4-, 9- and MyD88-deficient mice were cultured with 1 mg/ml KW3110 for 8 hrs and ROS production was measured. Data are mean ROS intensity 6 SD of three mice. * p,0.01 (Dunnett’s test). doi:10.1371/journal.pone.0035880.g005

References Powered by Scopus

Toll-like receptors

4937Citations
N/AReaders
Get full text

Toll-like receptors: Critical proteins linking innate and acquired immunity

4159Citations
N/AReaders
Get full text

Toll-like receptors and innate immunity

3472Citations
N/AReaders
Get full text

Cited by Powered by Scopus

Inhibition of curcumin on influenza A virus infection and influenzal pneumonia via oxidative stress, TLR2/4, p38/JNK MAPK and NF-κB pathways

208Citations
N/AReaders
Get full text

Probiotic Lactobacillus Strains Stimulate the Inflammatory Response and Activate Human Macrophages

187Citations
N/AReaders
Get full text

TLR3-triggered reactive oxygen species contribute to inflammatory responses by activating signal transducer and activator of transcription-1

73Citations
N/AReaders
Get full text

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Cite

CITATION STYLE

APA

Ichikawa, S., Miyake, M., Fujii, R., & Konishi, Y. (2012). MyD88 associated ROS generation is crucial for lactobacillus induced IL-12 production in macrophage. PLoS ONE, 7(4). https://doi.org/10.1371/journal.pone.0035880

Readers over time

‘12‘13‘14‘15‘16‘17‘18‘19‘20‘21‘22‘23‘240481216

Readers' Seniority

Tooltip

PhD / Post grad / Masters / Doc 15

60%

Researcher 8

32%

Professor / Associate Prof. 2

8%

Readers' Discipline

Tooltip

Agricultural and Biological Sciences 10

45%

Biochemistry, Genetics and Molecular Bi... 5

23%

Medicine and Dentistry 4

18%

Immunology and Microbiology 3

14%

Save time finding and organizing research with Mendeley

Sign up for free
0