• 제목/요약/키워드: Immunostimulatory activity

검색결과 78건 처리시간 0.029초

Effects of in vitro immune stimulation by ginsenoside Rb1

  • Kim, Ji-Young;Han, Eun-Hee;Jeong, Hye-Gwang
    • 고려인삼학회:학술대회논문집
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    • 고려인삼학회 2006년도 춘계학술대회
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    • pp.57-58
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    • 2006
  • Red ginseng is a classical traditional Chinese medicine. Among Chinese herbs, red ginseng has been considered as one of the tonics. Many studies indicated that red ginseng could enhance immune function of the human body. Red ginseng total saponin, ginsenoside, the most important active constituents identified in red ginseng can protect against myocardial ischaemia damage and protect endothelium against electrolysis-induced free radical injury. Macrophages play a significant role in host defense mechanisms. When activated, they inhibit the growth of a wide variety of tumor cells. The aim of this study was to determine the effects of pure ginsenoside Rb1 on immunostimulatory activity such as murine macrophage phagocytosis and proliferation of splenocytes. Furthermore, we investigated the effects of ginsenoside Rb1 on the production of nitric oxide (NO), reactive oxygen species (ROS) and proinflammatory cytokines (IL-1beta, IL-6, and TNF-alpha) in murine macrophage, RAW 264.7 cells. ROS have emerged as important signaling molecules in the regulation of various cellular processes. Ginsenoside Rb1 significantly increased production of ROS in dose dependent manner. As NO plays an important role in immune function, ginsenoside Rb1 treatment could modulate several aspects of host defense mechanisms due to stimulation. Treatment with ginsenoside Rb1 to macrophages induced the production of NO and proinflammatory cytokines and expression levels of these genes in a dose-dependent manner. Furthermore, incubation of RAW 264.7 cells with ginsenoside Rb1 showed a dose dependent increased phagocytosis activity and lymphocyte proliferation of splenocytes. Therefore, these results suggest that ginsenoside Rb1 has promising potential as a natural medicine for stimulation of the immune system.

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Screening of Lactobacilli Derived from Chicken Feces and Partial Characterization of Lactobacillus acidophilus A12 as Animal Probiotics

  • Lee, Na-Kyoung;Yun, Cheol-Won;Kim, Seung-Wook;Chang, Hyo-Ihl;Kang, Chang-Won;Paik, Hyun-Dong
    • Journal of Microbiology and Biotechnology
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    • 제18권2호
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    • pp.338-342
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    • 2008
  • This study was performed to screen and select Lactobacillus strains from chicken feces for probiotic use in animals. Of these strains, strain AU had the highest immunostimulatory effect. Therefore, strain A12 was characterized as a potential probiotic. Strain A12 was tentatively identified as Lactobacillus acidophilus A12, using the API 50 CHL kit based on a 99.9% homology. L. acidophilus A12 was highly resistant to artificial gastric juice (pH 2.5) and bile acid (oxgall). Based on results from the API ZYM kit, leucine arylamidase, crystine arylamidase, acid phosphatase, naphthol-AS-BI-phosphohydrolase, ${\alpha}$-galactosidase, ${\beta}$-galactosidase, ${\alpha}$-glucosidase, ${\beta}$-glucosidase, and N-acetyl-${\beta}$-glucosamidase were produced by strain A12. L. acidophilus A12 showed resistance to several antibiotics (nisin, gentamicin, and erythromycin). The amount of interleukin $(IL)-1{\alpha}$ in $20{\times}$ concentrated supernatant from L. acidophilus A12 was approximately 156pg/ml. With regard to antioxidant activity, L. acidophilus A12 supernatant showed 60.6% DPPH radical scavenging activity. These results demonstrate the potential use of L. acidophilus A12 as health-promoting probiotics.

길경배지 유산균이 마우스 대식세포의 NO 및 TNF-${\alpha}$에 미치는 영향 (Effects of Lactobacillus Plantarum Cultured in Platycodi Radix Decoction on the Eexpression of NO and TNF-${\alpha}$ in Mouse Macrophage RAW264.7 Cell Line)

  • 김성원;강희;안광석;심범상;김성훈;최승훈;안규석
    • 동의생리병리학회지
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    • 제23권2호
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    • pp.331-336
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    • 2009
  • This study examined the effects of Lactobacillus plantarum(LP) cultured in Platycodi Radix decoction(LPPR) on the expressions of NO and TNF-${\alpha}$ in mouse macrophage RAW264.7 cell line. Cells were stimulated with LP or LPPR (0.1, 1, and 10 bacteria/cell) in all assays. More NO was induced in LPPR than LPM at 0.1 and 1 of a LP: cell ratio. The iNOS mRNA expression was also enhanced in LPPR stimulated cells. TNF-${\alpha}$ was increased in LPPR stimulated cells at the protein and mRNA level compared with LPM. In conclusion, LP fermented in Platycodi Radix decoction induced stronger activity in NO and TNF in mouse macrophages than LPM. These results suggest that fermentation by Platycodi Radix can be useful in enhancing the immunostimulatory activity of LP.

T Cell Stimulatory Effects of Korean Red Ginseng through Modulation of Myeloid-Derived Suppressor Cells

  • Jeon, Chan-Oh;Kang, Soo-Won;Park, Seung-Beom;Lim, Kyung-Taek;Hwang, Kwang-Woo;Min, Hye-Young
    • Journal of Ginseng Research
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    • 제35권4호
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    • pp.462-470
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    • 2011
  • Myeloid-derived suppressor cells (MDSCs) actively suppress immune cells and have been considered as an impediment to successful cancer immunotherapy. Many approaches have been made to overcome such immunosuppressive factors and to exert effective anti-tumor effects, but the possibility of using medicinal plants for this purpose has been overlooked. Korean red ginseng (KRG) is widely known to possess a variety of pharmacological properties, including immunoboosting and anti-tumor activities. However, little has been done to assess the anti-tumor activity of KRG on MDSCs. Therefore, we examined the effects of KRG on MDSCs in tumor-bearing mice and evaluated immunostimulatory and anti-tumor activities of KRG through MDSC modulation. The data show that intraperitoneal administration of KRG compromises MDSC function and induces T cell proliferation and the secretion of IL-2 and IFN-${\gamma}$, while it does not exhibit direct cytotoxicity on tumor cells and reduced MDSC accumulation. MDSCs isolated from KRG-treated mice also express significantly lower levels of inducible nitric oxide synthase and IL-10 accompanied by a decrease in nitric oxide production compared with control. Taken together, the present study demonstrates that KRG enhances T cell function by inhibiting the immunosuppressive activity of MDSCs and suggests that although KRG alone does not exhibit direct anti-tumor effects, the use of KRG together with conventional chemo- or immunotherapy may provide better outcomes to cancer patients through MDSC modulation.

Dendritic Cell Activation by Glucan Isolated from Umbilicaria Esculenta

  • Kim, Hyung-Sook;Kim, Jee-Youn;Lee, Hong-Kyung;Kim, Moo-Sung;Lee, Sang-Rin;Kang, Jong-Soon;Kim, Hwan-Mook;Lee, Kyung-Ae;Hong, Jin-Tae;Kim, Young-Soo;Han, Sang-Bae
    • IMMUNE NETWORK
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    • 제10권6호
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    • pp.188-197
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    • 2010
  • Background: Lichen-derived glucans have been known to stimulate the functions of immune cells. However, immunostimulatory activity of glucan obtained from edible lichen, Umbilicaria esculenta, has not been reported. Thus we evaluated the phenotype and functional maturation of dendritic cells (DCs) following treatment of extracted glucan (PUE). Methods: The phenotypic and functional maturation of PUE-treated DCs was assessed by flow cytometric analysis and cytokine production, respectively. PUE-treated DCs was also used for mixed leukocyte reaction to evaluate T cell-priming capacity. Finally we detected the activation of MAPK and NF-${\kappa}B$ by immunoblot. Results: Phenotypic maturation of DCs was shown by the elevated expressions of CD40, CD80, CD86, and MHC class I/II molecules. Functional activation of DCs was proved by increased cytokine production of IL-12, IL-$1{\beta}$, TNF-${\alpha}$, and IFN-${\alpha}/{\beta}$, decreased endocytosis, and enhanced proliferation of allogenic T cells. Polymyxin B, specific inhibitor of lipopolysaccharide (LPS), did not affect PUE activity, which suggested that PUE was free of LPS contamination. As a mechanism of action, PUE increased phosphorylation of ERK, JNK, and p38 MAPKs, and enhanced nuclear translocation of NF-${\kappa}B$ p50/p65 in DCs. Conclusion: These results indicate that PUE induced DC maturation via MAPK and NF-${\kappa}B$ signaling pathways.

Effects of CpG Oligodeoxynucleotides on Immune Responses and Expression of Cytokine Genes in Cultured Olive Flounder Paralichthys olivaceus

  • Ahn, kyoung-Jin;Nam, Bo-Hye;Kim, Young-Ok;Kang, Jung-Ha;Kim, Bong-Seok;Jee, Young-Ju;Lee, Sang-Jun
    • Fisheries and Aquatic Sciences
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    • 제10권1호
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    • pp.1-7
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    • 2007
  • The induction of cellular and humoral immunity and cytokine gene expression by synthetic CpG oligodexoynucleotides (CpG-ODNs) has not been investigated systematically in olive flounder Paralichthys olivaceus in vivo. We optimized the proper concentration of CpG-ODNs using an in vitro assay for the superoxide anion $(O_2^-)$. CpG-ODNs induced $O_2^-$ and nitric oxide (NO) production, lysozyme activity, and the proinflammatory cytokine gene expression of $IL-1{\beta}$ and $TNF-{\alpha}$ in olive flounder significantly in vivo, whereas non-CpG-ODNs did not produce these effects or produced them to a lesser extent. This implied that CpG-ODNs could stimulate cellular and humoral immunity and cytokine gene expression in olive flounder. This is the first evidence of NO production and the first study on the mRNA expression of the proinflammatory cytokine genes $IL-1{\beta}$ and $TNF-{\alpha}$ in olive flounder in response to CpG-ODNs. Comparison of the variation in NO production and lysozyme activity to that of other studies led us to postulate that a group-specific difference exists in the immune responses of olive flounder against CpG-ODNs. Furthermore, the detailed immunostimulatory spectrum of CpG-ODNs in olive flounder could be a useful index with which to analyze the effect of CpG-ODNs against the challenge test prior to field applications.

RAW264.7 Cell Activating Glucomannans Extracted from Rhizome of Polygonatum sibiricum

  • Yelithao, Khamphone;Surayot, Utoomporn;Lee, Ju Hun;You, SangGuan
    • Preventive Nutrition and Food Science
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    • 제21권3호
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    • pp.245-254
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    • 2016
  • Water-soluble polysaccharides isolated from the rhizome of Polygonatum sibiricum and fractionated using ionexchange chromatography were investigated to determine their structure and immunostimulating activity. Crude and fractions ($F_1$ and $F_2$) consisted of carbohydrates (85.1~88.3%) with proteins (4.51~11.9%) and uronic acid (1.79~7.47%), and included different levels of mannose (62.3~76.3%), glucose (15.2~20.3%), galactose (4.35~15.3%), and arabinose (4.00~7.65%). The crude contained two peaks with molecular weights (Mw) of $151{\times}10^3$ and $31.8{\times}10^3$, but $F_1$ and $F_2$ exhibited one major peak with Mw of $103{\times}10^3$ and $628{\times}10^3$, respectively. Little immunostimulatory activity was observed by the crude; however, $F_1$ and $F_2$ significantly activated RAW264.7 cells to release nitric oxide and various cytokines, suggesting they were potent immunostimulators. The backbone of the most immunostimulating fraction ($F_1$) was ($1{\rightarrow}4$)-manno- and ($1{\rightarrow}4$)-gluco-pyranosyl residues with galactose and glucose attached to O-6 of manno-pyranoside.

방사선 방어효과 예측 가능한 면역증강 인삼 다당체의 활성인자 (Representative Parameter of Immunostimulatory Ginseng Polysaccharide to Predict Radioprotection)

  • 손혁진;심지영;안지연;윤연숙;송지영
    • Journal of Radiation Protection and Research
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    • 제33권3호
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    • pp.99-104
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    • 2008
  • 암 환자를 대상으로 방사선 치료빈도가 높아짐에 따라 다양한 작용 기전을 바탕으로 한 방사선 방어제 개발에 많은 노력을 경주하고 있다. 본 연구에서는 조혈, 면역세포의 증식과 다양한 싸이토카인의 분비를 증가시킴으로써 방사선 방어효능이 보고된 바 있는 인삼 다당체를 대상으로 화학적 구성성분과 각종 면역활성 지표 및 방사선 방어효능을 확인하고 가장 상관관계가 좋은 인자를 추출해내고자 하였다. 면역학적 활성으로는 임파구 증식능, 대식세포의 산화질소 분비능, AK세포 활성능을 검사하였으며 방사선 방어효과는 endogenous colony-forming unit(e-CFU)로 측정하였다. 인삼으로부터 추출된 다당체의 구성성분 중 galactose함량이 증가할수록 면역증강작용이 우수하였으며 임파구 증식능이 방사선 방어효과와 밀접한 관계가 있는 것으로 나타났다.

참당귀에서 분리한 다당의 면역활성에 대한 당쇄의 역할 (Roles of sugar chains in immunostimulatory activity of the polysaccharide isolated from Angelica gigas)

  • 신광순
    • 한국식품과학회지
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    • 제51권4호
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    • pp.336-342
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    • 2019
  • 참당귀 유래 면역활성 다당의 활성과 구조의 상관관계를 규명하고자 조다당 AGE-0로부터 두 차례의 연속적인 컬럼 크로마토그래피를 실행하여 단일 정제 다당 AGE-2c-I을 얻었다. AGE-2c-I은 농도의존적으로 우수한 항보체 활성을 보여주었으며, 일반화학적 특성을 분석한 결과, 분자량 약 140 kDa의 고분자 다당으로 4종의 구성당과 13종의 당쇄 결합양식으로 구성되어 있음을 확인할 수 있었다. 이 다당은 ${\beta}$-glucosyl Yariv reagent와의 높은 반응성을 보임으로써 arabino-3,6-galactan의 구조를 가진 rhamnogalacturonan-I 구조임을 추정할 수 있었다. 한편, AGE-2c-I의 미세구조의 해명과 항보체 활성에 관여하는 다당 중의 활성부위 검토를 위해 ${\alpha}$-L-arabinofuranosidase와 endo-1,4-${\beta}$-galactanase를 이용한 연속적 가수분해를 행하고 얻은 단편획분들을 이용, 구성당 및 당쇄결합 양식 분석, ${\beta}$-glucosyl Yariv reagent와의 반응성 검토 및 항보체 활성 결과를 분석한 결과, 참당귀 유래 항보체활성 다당 AGE-2c-I은 rhamnogalacturonan-I과 유사한 구조를 소유하고 있음이 확인되었으며, AGE-2c-I의 측쇄 구조인 arabino-${\beta}$-3,6-galactan 사슬이 항보체 활성 발현에 주요 역할을 수행하며, 5-linked Araf와 3,5-branched Araf로 구성된 ${\alpha}$-arabinan 측쇄가 활성에 부분적으로 관여하고 있음을 최종 확인할 수 있었다.

시판 인스턴트 커피에서 추출한 다당류의 화학적 특성 및 면역활성 (Chemical Characteristics and Immunostimulating Activity of Crude Polysaccharide Isolated from Commercial Instant Coffee)

  • 곽봉신;신광순
    • 한국식품과학회지
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    • 제48권3호
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    • pp.289-295
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    • 2016
  • 국내 시판중인 인스턴트 커피에서 다당류를 추출하여 새로운 면역 활성 물질을 확인하고자 하였다. 시판중인 인스턴트 커피를 구입하여 냉수추출 후, 에탄올 침전과 투석을 통하여 약 24%의 높은 수율로 다당류(ICP-0)를 얻을 수 있었다. ICP-0은 중성당 89.9%, 산성당 10.1%로 이루어진 다당체로써, 구성 성분으로는 갈락토스 55.5%, 만노스 25.7%와 소량의 아라비노스, 람노스 등으로 이루어진 것을 확인하였으며, 갈락토만난(galactomannan)이나 팩틴 다당류(pectic polysaccharide)가 혼합된 구조일 것이라고 추정되었다. 인스턴트 커피 유래 ICP-0에 대하여 대식세포 자극에 대한 세포증식능을 확인한 결과, NC 대비 유의적으로 높은 증식활성을 보였으며, IL-6, IL-12 및 TNF-${\alpha}$의 경우, $10{\mu}g/mL$에서도 NC 대비 우수한 사이토카인 분비 유도능을 보임이 확인되었다. 또한 NO, ROS를 분석한 결과에서도 NO의 경우 $10{\mu}g/mL$ 이상에서 NC 대비 양호한 활성을 보여 주었다. ICP-0에 대하여 2차 면역기관 중 하나인 비장세포상의 증식능을 확인한 결과, NC 대비 115% 정도 증식하는 것이 확인되어 면역세포를 직접 증진시키는 마이토겐 활성이 있음을 나타내었다. 인스턴트 커피 유래 ICP-0가 장관 내 분포되어 있는 Peyer's patch를 경유하여 장관면역에 공헌할 수 있는지 여부를 확인한 결과, NC 대비 유의적으로 골수세포의 증식능을 확인하였으며 GM-CSF와 같은 관련 사이토카인의 분비 유도가 확인되었다. 이상의 결과는 시판 인스턴트 커피로부터 분리한 다당류가 대식세포의 기능과 장관면역계를 증진시킬 수 있는 가능성을 제시한다.