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Immune modulation of cholera toxin and Bacillus subtilis spore delivered intranasally to mouse : 마우스 비강으로 전달된 콜레라 톡신과 바실러스 서브틸리스 포자의 면역 조절 작용
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- Authors
- Advisor
- 윤철희
- Major
- 농업생명과학대학 농생명공학부
- Issue Date
- 2014-02
- Publisher
- 서울대학교 대학원
- Keywords
- immune modulation ; cholera toxin ; bacillus subtilis spore ; intranasal ; lung ; chemokine ; cytokine
- Description
- 학위논문 (석사)-- 서울대학교 대학원 : 농생명공학부, 2014. 2. 윤철희.
- Abstract
- In the respiratory system, chemokines, cytokines and antimicrobial peptides (AMPs) play important roles for regulation of immune response. AMPs can protect the foreign molecules and chemokines can recruit the leukocytes that can remove the pathogen. Cytokines can enhance the effect of AMPs and chemokines and activate various immune cells.
The mucosal adjuvant has been studied by many researchers. Cholera toxin (CT), lipopolysaccharide (LPS) and Bacillus subtilis spore were, also, examined for the development of mucosal adjuvant. However, the effects of these adjuvants have not been understood completely through the administration of intranasal route in the lung and bronchoalveolar lavage fluid (BALF).
In the present study, the effect of the mucosal adjuvants, CT, B. subtilis spore and LPS, was examined by the analysis on the expression of effector molecules and migration of leukocytes in the lung. The adjuvants, CT, B. subtilis spore or LPS, were administered through the intranasal route to mice maintained at SPF facility. Then lung, BALF and serum were taken from the mice at 6, 12, 24 and 72 hr and analyzed mRNA and protein levels of effector molecules. Furthermore, the migration of cells into BALF was examined through analysis of the surface marker using flow cytometer.
The results showed that mRNA of CCL2, CCL4 and CXCL10 were induced by spore or LPS in the lung. However, there are no differences on the mRNA expression of AMPs between the adjuvants. Spore and LPS promoted the expression and secretion of CCL2 and CCL4 proteins in the lung and BALF. In analysis of pro-inflammatory cytokines, spore and LPS dramatically induced the secretion of IL-1β, IL-6 and TNF-α in the lung and BALF. CT induced the increase of IL-6 in the serum. In analysis of surface marker, spore highly promoted the migration of Gr-1+CD11b+ cells at 6 hr and F4/80+CD11b+Gr-1- cells at 72 hr. LPS, also, induced the migration of Gr-1+CD11b+ cells at 12 and 24 hr. In conclusion, B. subtilis spore can induce the chemokine and cytokine expression in the lung and BALF and enhance the migration of neutrophils into BALF.
- Language
- English
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