• 제목/요약/키워드: phagocytic activity

검색결과 306건 처리시간 0.036초

개 말초혈액 탐식세포의 탐식반응에 대한 1,2-benzopyrone의 면역자극 효과 (Immunostimulating Effect of 1,2-Benzopyrone on Phagocytic Response of Canine Peripheral Blood Phagocytes)

  • 신정화;나기정;양만표
    • 한국임상수의학회지
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    • 제21권1호
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    • pp.23-28
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    • 2004
  • 1,2-benzopyrone has been shown to affect on the activation and stimulation of macrophage. To examine the immunostimulating effect of 1,2-benzopyrone on the phagocytic response of canine peripheral blood mononuclear cells (PBMC) as well as polymorphonuclear cells (PMN), the phagocytic activity of phagocytes was analyzed by flow cytometry system using FITC-labelled latex. The 1,2-benzopyrone did not show any direct effect on phagocytic response of PBMC and PMN. But it showed an enhanced effect on the phagocytic response of monocyte-rich cells fractioned by cell size from dot plot profile in flowcytometric cytography of PBMC. The phagocytic activity of these cells was also enhanced by addition of culture supernatant from PBMC treated with 1,2-benzopyrone. Similarly, the phagocytic activity of PMN but not PBMC in the same procedures was enhanced by culture supernatant from PBMC treated with 1,2-benzopyrone. However, the culture supernatant from PMN treated with 1.2-benzopyrone did not show the enhancing effect on phagocytic activity for monocyte-rich cells and PMN. These results, therefore, suggested that enhanced phagocytic activity of canine peripheral blood PMN and monocytes may be mainly mediated by humoral factor(S) released from PBMC treated with 1,2-benzopyrone.

고양이 말초혈액 탐식세포의 탐식능에 있어서 계난백유래물질의 효과 (Effect of Egg White Derivatives on Phagocytic Response of Feline Peripheral Blood Phagocytes)

  • 양만표;김기홍
    • 한국임상수의학회지
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    • 제16권1호
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    • pp.37-41
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    • 1999
  • The immunostimulating effects of egg white derivatives (EWD) on the phagocytic response of feline peripheral blood polymorphonuclear cells (PMN) as well as mono- nuclear cells (MNC) were examined. The phagocytic activity was analyzed by a flow cytometry system. The EWD showed directly an enhanced effect on the phagocytic response of MNC but not PMN. The phagocytic activity of MNC was enhanced by culture supernatant from MNC and PMN treated with EWD, respectively. Similarly, the phagocytic activity of PMN was enhanced by culture supernatant from MNC but not PMN treated with EWD. It was, therefore, indicated that the enhanced phagocytic activity of feline PMN could be mainly mediated by humoral factor(s) released from MNC treated with EWD. These results suggested that EWD could enhance the phagocytosis of feline peripheral blood phagocytes.

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계난백유래물질로 배양한 고양이 말초혈액 단핵구세포 배양상층액중의 탐식촉진인자 검출 (Detection of Phagocytosis-Promoting Factor of Culture Supernatant from Feline Peripheral Blood Mononuclear Cells Cultured with Egg White Derivatives)

  • 양만표;김기홍
    • 한국임상수의학회지
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    • 제16권1호
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    • pp.31-36
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    • 1999
  • The aim of this study is to determine the phagocytosis-promoting factor(s) for feline peripheral blood polymorphonuclear cells (PMN) by culture supernatant from mono-nuclear cells (MNC) treated with egg white derivatives (EWD). The phagocytic activity of PMN was analyzed by a flow cytometry system. The EWD did not show direct effect on the phagocytic response of PMN. The phagocytic activity of PMN was enhanced by culture supernatant from MNC but not PMN treated with EWD. Therefore, it was suggested that the enhanced phagocytic activity of feline PMN could be mediated by humoral factor(s) released from MNC treated with EWD. Thus, the phagocytosis-promoting factor(s) in supernatant fraction from MNC culture treated with EWD were isolated by reverse phase high pressure liquid chromatography. The resulting supernatant fraction on 29.02 minutes of retention time showed high phagocytic activity of PMN. The molecular weight of this supernatant fraction was 16 to 18 kDa when analyzed by capillary electrophoresis. The isoelectric point was pH 5.76 when assessed by ion-exchange chromatography. These results suggest that EWD stimulates feline MNC to elaborate a phagocytosis-promoting factor, 16 to 18 kDa of molecular weight, which could be an important mediator for the enhancement of phagocytic activity of feline peripheral blood phagocytes. Further study will be needed to elucidate this phagocytic factor.

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리포포리사카라이드의 세포성 면역반응에 미치는 스와인소닌의 영향 (Effects of Swainsonine on the Cell-mediated Immune Responses of Lipopolysaccharide)

  • 채병숙;안영근;김정훈
    • 약학회지
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    • 제42권1호
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    • pp.75-81
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    • 1998
  • Effects of swainsonine (SW: 8${\alpha}$, ${\beta}$-indolizidine-1alpha, 2${\alpha}$, 8${\beta}$-triol from Locoweed) on the cellular and nonspecific immune responses of lipopolysaccharide (LPS) wer e studied in ICR mice. Mice were divided into 4 groups (10mice/group), and LPS was given to each mouse 1 hr after i.p. injection with 3.7mg/kg of SW by i.p. injection twice a week for 14 days at a dose of 2mg/kg. Immune responses of the delayed-type hypersensitivity response (DTH) to sheep red blood cells (s-RBC), phagocytic activity and natural killer (NK) cell activity were evaluated. LPS treatment didn`t affect NK cell activity, phagocytic activity, DTH to s-RBC compared with those in controls, and phagocytic activity of sareoma 180 tumor bearing mice. However, circulating leukocytes were significantly decreased. Combinaton of LPS and SW increased circulating leukocytes significantly compared vath that in LPS alone, and DTH to s-RBC, NK cell activity and phagocytic activities of normal and sarcoma tumor bearing mice were not affected. These findings indicate that SW didn`t affected the cellular immune responses suppressed by LPS but significantly increased circulating leukocytes.

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C 반응성 단백질이 사람 Macrophage 탐식 기능에 미치는 영향 (Modulation of Human Macrophage Phagocytic Activity by C-reactive Protein)

  • 김용호;강신원
    • 대한의생명과학회지
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    • 제4권1호
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    • pp.35-42
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    • 1998
  • 치료목적으로 채취한 사람 복수에서 C반응성 단백질 (CRP)을 분리 정제하여 사람 대식세포 탐식활성에 미치는 영향에 대하여 연구하였다. CRP는 p-diazonium phenyl-phosphoryl choline 혹은 C-polysaccharide coupled sepharose 4B와 hydroxylapatite affinity chromatography법으로 분리 정제 시켰다. 대식 세포는 ficoll hypaque 밀도 원심 구배법으로 분리시킨 다음 부착법으로 정제시키고 탐식 시험을 이용하여 확인하였다. CRP가 대식 세포의 시험 관내 미생물 탐식 활성에 미치는 영향은 촉진 혹은 억제시키는 경향을 보였다. 즉, CRP와 대식세포 미생물 탐식능과의 관계는 반응시킨 시간, 반응계에 가해준 CRP량, 미생물ㆍ탐식세포 및 CRP상호간 반응시킨 순서에 따라서 다르게 나타났다. 대식세포의 시험관내 탐식활성에 미치는 CRP 자극의 특성은 한계자극 특성을 보였다.

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Phagocytic osteoclasts in the alveolar bone of diabetic rats with periodontitis

  • Bak, Eun-Jung;Kim, Ae Ri;Kim, Ji-Hye;Yoo, Yun-Jung
    • International Journal of Oral Biology
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    • 제45권3호
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    • pp.92-98
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    • 2020
  • Periodontitis is a bacteria-induced inflammatory disease associated with alveolar bone loss. Osteoclast is a macrophage-lineage cell that exhibits phagocytic activity; however, osteoclast phagocytic activity has not been demonstrated under pathological conditions. Diabetes is a pathological condition that exacerbates alveolar bone loss via periodontitis; therefore, we examined phagocytic osteoclasts in diabetic rats that had periodontitis. The rats were divided into the control (C), periodontitis (P), and diabetes with periodontitis (DP) groups. Diabetes and periodontitis were induced by streptozotocin injection and ligature of the mandibular first molars, respectively. On days 3 and 20 after the ligature, the rats were sacrificed, and osteoclasts containing inclusions were quantified by tartrate-resistant acid phosphatase staining. On day 3, there were more osteoclasts containing inclusions in the DP group than in the C group. Among inclusions, osteocyte-like cells and dense bodies were more frequently observed in the DP group than in the C group. Cytoplasm-like structures were elevated more in the DP group than in the C and P groups. However, no differences were observed on day 20. Interestingly, some osteoclasts were in contact with the osteocytes within the exposed lacunae and contained several inclusions within a large vacuole. Thus, the elevation of phagocytic osteoclasts in rats with diabetes and periodontitis provides insight into the role of osteoclast phagocytic activity under pathological conditions.

우리밀의 면역증강능 규명 (Screening of Immune-Enhancing Substance(s) from Korean Wheats)

  • 최면;박재봉;김현숙
    • 한국식품영양과학회지
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    • 제29권2호
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    • pp.307-311
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    • 2000
  • The purpose of this study was to identify excellent immune-enhancing substance from Korean wheats(Eunpa, Gueru, Alchan, Topdong, Suwon 267, Gobun) compared with imported ones(Australian standard white, ASW; Dark northern spring, DNS). Phagocytic activities of PBS (phosphate buffered saline, pH 7.4) and EA(ethanol-acetic acid) extracts from the wheats were determined using mouse macrophage J774 cell line. In order to set the optimal experimental condition up, the cultured cells were tested in varying experimental conditions. About two to five times higher phagocytic activity was shown in EA extract of Korean wheats compared to that of imported wheats. PBS extracts of wheats did not show increased phagocytic activity compared to control that did not add any extract. The EA extract of Gobun wheat showed the highest phagocytic activity. From the experiment we found that the optimal experimental condition was shown in two hours of reaction time and 0.05mg amout of EA extract added to J774 cells.

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국내산 밤 일부 품종의 기능성 성분분석과 항산화 및 대식세포 활성 (Antioxidative and Macrophage Phagocytic Activities and Functional Component Analyses of Selected Korean Chestnut (Castanea crenata S. et Z.) Cultivars)

  • 이현주;정미자;조재열;함승시;최면
    • 한국식품영양과학회지
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    • 제37권9호
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    • pp.1095-1100
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    • 2008
  • 국내산 밤 일부 품종(단택, 대보, 석추, 옥광, 병고)의 기능성 성분 분석과 이들 물질들의 항산화력 및 밤 추출물이 대식세포 활성에 미치는 영향력을 알아보았다. 국내산 밤 일부 품종의 내피와 과육에서 coumarin, gallic acid 그리고 catechin이 HPLC에 의해 검출되었다. 밤 내피에 가장 풍부한 기능성 성분은 catechin이고 그 다음 gallic acid와 coumarin 순이었으나, 과육에서는 gallic acid만 검출되었다. 따라서 밤의 기능성 성분인 gallic acid와 catechin의 항산화력을 DPPH radical 소거작용과 SOD 유사활성을 통해 알아보았다. Gallic acid과 catechin을 6.0 mg/100 g 처리하였을 때 DPPH radical 소거작용이 각각 69.4%와 38.3%였으며, gallic acid의 DPPH radical 소거작용은 농도 의존적이었다. Gallic acid를 동일한 농도의 catechin과 비교하면 모든 농도 구간에서 catechin보다 gallic acid가 높은 DPPH radical 소거활성을 나타내었다. 그러나 SOD 유사활성은 gallic acid보다 catechin이 높았다. 더하여 밤의 과육, 노란과육 및 흰과육 추출물들이 대식세포 활성에 미치는 영향력을 알아보았다. 병고 흰과육 추출물은 현저하게 대식세포 활성을 증가시켰고, 병고, 단택, 대보 및 옥광의 노란과육 추출물 역시 아무 것도 처리하지 않은 세포와 비교하여 현저히 대식세포를 활성화시켰다. 노란과육 추출물이 흰과육 추출물보다 더욱 더 대식세포 활성을 증가시켰고, 5품종 중 병고가 대식세포 활성을 가장 증가시켰다.

In Vitro에서 개 말초혈액 탐식세포의 탐식능에 대한 케타민의 효과 (Ketamine Decreases Phagocytic Capacity of Canine Peripheral Blood Phagocytes In Vitro)

  • 강지훈;김민준;양만표
    • 한국임상수의학회지
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    • 제25권2호
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    • pp.73-78
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    • 2008
  • 케타민은 N-methyl-D-aspartate (NMDA) 수용체의 비경쟁적인 길항제로 인의와 수의학에서 전신 마취제로 사용하는 약물이다. 본 연구진은 이전에 케타민이 개 말초혈액 백혈구의 순간산소과소비현상(oxidative burst activity)을 손상시킨다고 보고하였다. 현재 연구에서는 개 말초혈액 탐식세포의 탐식능(phagocytic capacity)에 대한 케타민의 효과를 검토하였다. 탐식능은 유세포 분석기로 분석하였다. 말초혈액 다형핵백혈구(peripheral blood polymorphonuclear cells; PMN)와 단구(monocytes)의 탐식능은 케타민의 직접 처리에 의해 감소하였으나 단핵구세포(peripheral blood mononuclear cells; PBMC) 분획에서의 탐식능은 케타민의 직접 처리에 의해 변화가 없었다. 말초혈액 다형핵백혈구와 단구의 탐식능은 케타민을 처리한 단핵구세포 배양상층액에 의해서도 감소하였다. 이상의 결과로부터 케타민은 호중구와 단구와 같은 개 말초혈액 탐식세포의 탐식능에 있어 직접적인 억제효과를 나타내며, 또한 케타민 처리 단핵구세포로부터 생산되는 가용성인자에 의해서도 탐식세포의 탐식능이 억제되는 것으로 사료되었다.

Immunoregulation Effect of KamiBohuh-tang

  • Park Kyung Mi;Jung Jin Hong;Yoo Dong Youl
    • 동의생리병리학회지
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    • 제16권1호
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    • pp.186-191
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    • 2002
  • The purpose of this study is to prove the efficacy of KamiBohuh-tang(KBT) on immunoregulation and the possibility of KBT as an immunoadjuvant. KBT with solid feed was administered orally once a day for 7 days to an experimental group, a solution of salt and solid feed without KBT to a control group. After a week T cell, B cell, cytokines, nitric oxide and phagocytic activity are measured. KBT enhanced the proliferation of splenocytes and the subpopulation of Th cells in splenic T-Iymphocytes, but did not affect the proliferation of thymocytes. KBT decreased the subpopulation of T-Iymphocytes in splenocytes. KBT enhanced the production of interferon-γ. interleukin-2, interleukin-4 in mice serum and the phagocytic activity in peritoneal macrophages but it suppressed the production of nitric oxide. These results suggest that KBT is a potent prescription on immune response via the increase of the proliferation of splenocytes, the production of cytokines from splenic Th cells and the phagocytic activity in vivo.