The Modulatory Effect of Sodium Propionate Treatment in the Expression of Inflammatory Cytokines and Intracellular Growth of Brucella abortus 544 in Raw 264.7 Cellsopen accessThe Modulatory Effect of Sodium Propionate Treatment in the Expression of Inflammatory Cytokines and Intracellular Growth of Brucella abortus 544 in Raw 264.7 Cells
- Other Titles
- The Modulatory Effect of Sodium Propionate Treatment in the Expression of Inflammatory Cytokines and Intracellular Growth of Brucella abortus 544 in Raw 264.7 Cells
- Authors
- Kim Heejin; Huy Tran Xuan Ngoc; Nguyen Trang Thi; Reyes Alisha Wehdnesday Bernardo; Min Wongi; Lee Hu Jang; Hur Jin; Kim Suk
- Issue Date
- Aug-2023
- Publisher
- 한국미생물·생명공학회
- Keywords
- Brucella abortus; sodium propionate; macrophages; cytokines; NF-κB; Brucella abortus; sodium propionate; macrophages; cytokines; NF-κBv
- Citation
- Journal of Microbiology and Biotechnology, v.33, no.8, pp 1006 - 1012
- Pages
- 7
- Indexed
- SCIE
SCOPUS
KCI
- Journal Title
- Journal of Microbiology and Biotechnology
- Volume
- 33
- Number
- 8
- Start Page
- 1006
- End Page
- 1012
- URI
- https://scholarworks.gnu.ac.kr/handle/sw.gnu/67752
- DOI
- 10.4014/jmb.2303.03041
- ISSN
- 1017-7825
1738-8872
- Abstract
- In this study, we investigated the effects of sodium propionate (SP) treatment on intracellular mechanism of murine macrophages and its contribution to host immunity during Brucella abortus 544 infection.
The intracellular growth assay revealed that SP inhibited Brucella replication inside the macrophages.
To determine intracellular signaling involved during SP treatment after Brucella infection, we analyzed the change of five different cytokines production relevant to SP such as TNF-α, IL-10, IFN-γ, IL-1β, and IL-6, and the results indicated that the boost with IL-10 was apparent throughout the culture period for 48 h as well as IL-1β which was apparent at 24 h post-infection and IFN-γ which was apparent at 24 h and 48 h in comparison to SP untreated groups. On the other way, SP-treated cells displayed suppressed production of TNF-α and IL-6 at all time points tested and 48 h post-infection, respectively. Furthermore, we conducted western blot to establish a cellular mechanism, and the result suggested that SP treatment attenuated p50 phosphorylation, part of the NF-κB pathway.
These findings indicated that the inhibitory effect of SP against Brucella infection could be attributed through induction of cytokine production and interference on intracellular pathway, suggesting SP as a potential candidate for treating brucellosis.
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Collections - 학과간협동과정 > 수의생명공학과 > Journal Articles
- 수의과대학 > Department of Veterinary Medicine > Journal Articles
- 의학계열 > 수의학과 > Journal Articles

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