• 제목/요약/키워드: Migration of neutrophil

검색결과 21건 처리시간 0.037초

Promotion of formyl peptide receptor 1-mediated neutrophil chemotactic migration by antimicrobial peptides isolated from the centipede Scolopendra subspinipes mutilans

  • Park, Yoo Jung;Lee, Sung Kyun;Jung, Young Su;Lee, Mingyu;Lee, Ha Young;Kim, Sang Doo;Park, Joon Seong;Koo, JaeHyung;Hwang, Jae Sam;Bae, Yoe-Sik
    • BMB Reports
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    • 제49권9호
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    • pp.520-525
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    • 2016
  • We investigated the effects of two antimicrobial peptides (AMPs) isolated from Scolopendra subspinipes mutilans on neutrophil activity. Stimulation of mouse neutrophils with the two AMPs elicited chemotactic migration of the cells in a pertussis toxin-sensitive manner. The two AMPs also stimulated activation of ERK and Akt, which contribute to chemotactic migration of neutrophils. We found that AMP-stimulated neutrophil chemotaxis was blocked by a formyl peptide receptor (FPR) 1 antagonist (cyclosporin H); moreover the two AMPs stimulated the chemotactic migration of FPR1-expressing RBL-2H3 cells but not of vector-expressing RBL-2H3 cells. We also found that the two AMPs stimulate neutrophil migration in vivo, and that this effect is blocked in FPR1-deficient mice. Taken together, our results suggest that the two AMPs stimulate neutrophils, leading to chemotactic migration through FPR1, and the two AMPs will be useful for the study of FPR1 signaling and neutrophil activation.

비스테로이드성 항염증제가 FMLP에 의한 사람 중성구의 이동에 미치는 영향 (Effects of Non-Steroidal Anti-Inflammatory Drugs on the FMLP-Induced Migration of Neutrophil)

  • 김우미;강구일
    • 대한약리학회지
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    • 제30권1호
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    • pp.137-143
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    • 1994
  • 본 연구는 7종의 비스테로이드성 항염증제가 FMLP에 의한 사람 중성구의 이동에 미치는 영향을 약물의 농도별로 관찰하고자, Hypaque-Ficoll step gradient centrifugation방법에 의하여 중성구를 분리하고, 48-well micro chemotaxis assembly를 이용하여 chemotactic assay를 시행하여 다음과 같은 결과를 얻었다. Oxyphenbutazone, phenylbutazone, zomepirac, ibuprofen은 약물의 치료 농도하에서 중성구의 이동에 대한 강력한 억제작용을 나타내었으며, indomethacin은 중성구의 이동을 오히려 증가시키는 작용을 나타내었다. 이 약제들은 모두 100uM미만의 약물 농도에서 각각 IC50를 나타내었으며, oxyphenbutazone, phenylbutazone은 10uM에서 최대 억제효과를 나타내었고, zomepirac, ibuprofen은 각각 0.luM과 100uM에서 가장 강한 억제 작용을 나타내었다. 또한 상기 약제를 FMLP와 함께 하단 구획에 첨가하였을 때에는 세포와 함께 상단구획에 첨가하였을 때와는 상이하게 세포의 이동에 전혀 영향을 미치지 못하였다. 이러한 결과는 이 약제가 FMLP와의 분자적 상호 작용을 통하여 FMLP의 작용을 저하시키는 것보다는 세포에 직접적인 영향을 미침으로서 세포의 이동을 억제하였음을 나타내어 준다. 이상의 연구 결과에서, oxyphenbutazone등의 약제가 100uM미만의 저농도에서 FMLP에 의한 중성구의 이동을 강력하게 억제하는 작용이 있음을 보고, 이 작용은 지금까지 비스테로이드성 함염증제의 작용 기전으로 말려진 cyclooxygenage 억제 작용과는 별개의 기전으로 사료되므로, 이를 상기 약제가 세포 수준에서 나타내는 제 2의 약리 기전으로 제시한다.denosine의 효과를 길항함을 볼 수 있었으나 $K{^+}$-통로 차단제인 glibenclamide는 adenosine의 효과에 영향을 미치지 못하였다. 8-Bromo-cAMP (100과 $300{\mu}M$) 그 자체로는 ACh 유리에 별다른 영향을 미치치 못하였으나 $300\;{\mu}M$ 8-bromo-cAMP 전처리에 의하여 $30\;{\mu}M\;adenosine$의 효과가 억제됨을 볼 수 있었다. 이상의 실험결과로 흰쥐 해마에서 $A_1-adenosine$ 수용체를 통한 adenosine의 ACh유리 감소는 G-단백에 의존적이며, 이러한 효과에 nifedipine에 예민한 $Ca^{++}$-통로와 adenylate cyclase계가 일부 관여함은 확실하나 proteinkinase C 및 glibenclamide에 예민한 $K{^+}$통로는 관여하지 않는 것으로 사료된다.(新稱), Phellinus pomaceus), 회주름구멍버섯(신칭(新稱), Antrodia crassa), 층주름구멍버섯(신칭(新稱), Antrodia serialis), 흰그물구멍버섯(신칭(新稱), Ceriporia reticulata), 겹친손등버섯(신칭(新稱), Oligoporus balsameus), 점박이손등버섯(신칭(新稱), Oligoporus guttulatus), 무른흰살버섯(신칭(新稱), Oxyporus cuneatus), 각목버섯(신칭(新稱), Rigidoporus microporus), 및 주름옷솔버섯(신칭(新稱), Trichaptum laricinum)으로서 우리말 이름과 영문 기재(記載)와 함께 우리나라의 균류목록(菌類目錄)에 새로이 추가되었다. 이였으며, White+NAA

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Levamisole, selenium 및 tocopherol이 한국재래산양의 혈중 호중구 및 복강 대식구의 기능에 미치는 영향 (Effects of levamisole, selenium and tocopherol on the functions of blood neutrophil and peritoneal macrophage of Korean native goats)

  • 김종만;마점술;전윤성
    • 대한수의학회지
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    • 제31권3호
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    • pp.285-294
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    • 1991
  • In this study, the immunomodulating effects of levamisole, selenium and tocopherol on blood neutrophils and peritoneal macrophages of goat were evaluated in vitro and in vivo. The functions of blood neutrophils and peritoneal macrophages were assayed by random and direct migration, phagocytosis of S aureus, production of superoxide and hydrogen peroxide. The results obtained were summarized as follows: In vitro trials 1. Levamisole treatment enhanced the random and direct migration of goat blood neutrophils when compared with untreated cell, and a significant (p<0.01) enhancement was noticed at the concentration of $100{\mu}g$ for direct migration and $50{\mu}g{\sim}1,000{\mu}g\;per\;ml$ of culture medium for random migration. There was no influence of selenium and tocopherol on random and direct migration of neutrophil at all of treatment concentration. 2. Neutrophils produced higher levels of superoxide by lcvamisole treatment at the concentration of $100{\mu}g$ and by selenium treatment at the concentration of $1.0{\mu}g$, but the production of hydrogen peroxide was not increased. Tocopherol had no effect on the production of antimicrobicidal oxygen metabolites of neutrophils at various concentrations. 3. No differences of phagocytic activity were observed when neutrophils were treated with three substances. In vivo trials 1. Blood neutrophils of goats orally administered levaraisole showed significantly (p<0.05) higher random migration from 2 to 24 hours after feeding (2.5mg/kg of body weight). Augmentation of random migration of neutrophil from goats orally administered selenium-tocopherol mixture (selenium $100{\mu}g$-tocopherol 200IU/head/day) was observed at 10 days and the significant (p<0.05) increase was shown from 30 days after feeding and continued throughout the feeding periods. 2. There was no effect on phagocytic activity and production of antimicrobicidal oxygen metabolites of neutrophils from goats administered levamisole or selenium-tocopherol mixture. 3. Random migration, production of superoxide and hydrogen peroxide and S aureus phagocytic activity of peritoneal macrophages of goats administered 300ml of levamisole-thioglycollatc medium mixture $(2.5{\mu}g/ml)$ into peritoneal cavity increased significantly (p<0.01 or p<0.05) when compared with those of goats administered thioglycollate medium alone.

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3 차원 주화성 모델 개발을 통한 흡착형 세포의 동적특성 연구

  • 송지환;김동철
    • 대한기계학회:학술대회논문집
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    • 대한기계학회 2008년도 추계학술대회A
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    • pp.1638-1642
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    • 2008
  • Cell migration is one of the essential mechanisms responsible for complex biological processes. Intensive researches have begun to elucidate the mechanisms and search intriguing conditions for efficient control of cell migration. One general mechanism which is widely applicable for cells including neutrophil, Escherichia coli and endothelial cell is chemotaxis. Especially, understanding the chemotactic mechanics of cell crawling has important implications for various medical and biological applications. The single cell study for chemotaxis has an advantage over studies with the population of cells in providing a clearer observation of cell migration, which leads to more accurate assessments of chemotaxis. In this paper, we propose a three-dimensional model considering a single crawling cell to study its chemotaxis. The semi-implicit Fourier spectral method is applied for high efficiency and numerical stability. The simulation results reveal rich dynamics of cell.

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Induction of the Neutrophil Migration in Normal Subjects due to Asthmatic Bronchoalveolar Lavage Fluid (BALF)

  • Lee, Ji-Sook;Choi, Eugene;Yang, Eun Ju;Lee, Na Rae;Baek, Seung Yeop;Kim, Eun Jeong;Kim, In Sik
    • 대한의생명과학회지
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    • 제20권3호
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    • pp.111-116
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    • 2014
  • Human neutrophils play an essential role in the innate immune response and are involved in the pathogenesis of the severe and corticosteroid-resistant asthma. Asthma is characterized by an infiltration of inflammatory cells into the lung and by a cytokine release. The aim of this study is to investigate the effects of a bronchoalveolar lavage fluid (BALF) on the chemotaxis and apoptosis of neutrophils which were isolated from healthy subjects. The BALF of subjects with asthma induces the blood neutrophil chemotaxis in the opposite of that in normal subjects. The IL-8, IL-6, and monocyte chemoattractant protein-1 (MCP-1) levels in BALF were higher in subjects with asthma than in normal subjects. The BALF of normal and asthmatic subjects has no effect on neutrophil apoptosis of BALF. MCP-1 delays the constitutive apoptosis of normal blood neutrophils, but has no effect in normal BALF neutrophils. These results may indicate that inflammatory factors secreted by the lung tissue of patients with asthma trigger the neutrophil chemotaxis and also induce the neutrophil dysregulation.

백혈구 CD11b에 대한 단 클론 항체 (MAb 1B6)는 Spraque Dawley의 E. coli 폐렴의 조기 사망률을 증가시킨다 (Monoclonal Antibody against leucocyte CD11b(MAb 1B6) increase the early mortality rate in Spraque Dawley with E. coli pneumonia)

  • 김형중;김성규;이원영
    • Tuberculosis and Respiratory Diseases
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    • 제43권4호
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    • pp.579-589
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    • 1996
  • 연구배경 : 패혈증에서 백혈구의 활성화는 미생물 및 숙주 독성 물질의 청소에 중요한 역활을 하며 한편으로 활성화된 호중구와 그의 특성 물질은 조직 손상파 장기의 기증 부전을 초래한다. 백혈구의 CD11/18 유착 분자는 감염 및 염증 부위로 호중구 이동의 첫 단계인 호중구-내피 세포 유착을 조절한다. 패혈증 치료 전락으로 호중구 억제 효과의 가능성을 알아보기 위해 rat 에서 Escherichia coli 폐렴을 유발하여 CD11b에 대한 단클론 항체(MAb 1B6)의 효과를 평가하였다. 방법 : 1 mg/kg CD11b에 대한 단클론 항체와 1 mg/kg BSA출 폐렴 유발 6 시간전, 유발시 및 유발 6 시간후 무작위적으로 피하 투여하였다. 폐렴 유발후 무작위적으로 24, 60 및 90%의 산소를 투여하였으며 폐렴 유발후 4시간 및 3일간 하루에 한번씩 100 mg/kg의 ceftriaxone을 투여하였다. 말초 및 폐포 호중구와 폐 손상의 지표인 D(A-a)O2, W/D LW ratio 및 폐포 세척액 단백 농도를 12시간과 96시간까지 생존한 동물에서 측정하였다. 결과 : CD11b에 대한 단클론 항체는 말초 및 폐포 호중구를 감소시켰으며 96시간 보다 12시간에 더욱 감소시켰다. 폐손상 지표는 단클론 항체 투여군과 대조군을 비교시 차이를 보이지 앉았으나 생존 동물 수의 부족으로 통계학적 평가의 의미가 없었다. 조기(6 시간) 사망률은 항체 투여군 51%로 대조군 31%보다 의미(P=0.02) 있게 증가하였으나 후기 사망률(12 시간에서 72 시간)은 항체 투여군 44% 대조군 36%로 의미(P=0.089) 있는 차이가 없었다. 결론 : CD11b/18 유착 분자는 감염 및 염증 부위로 호중구의 이동을 조절하는 것으로 알려져 있다. CD11b에 대한 단클론 항체는 rat의 폐인성 패혈증에서 폐포 호중구를 감소시키고 조기 사망률을 증가시켰다. 따라서 CD11b에 대한 단클론 항체가 rat의 폐인성 패혈증의 초기에 호중구의 폐포내 이동을 억제시켜 숙주의 방어 기전에 장애를 초래하여 조기 사망률을 증가시키는 것으로 사료된다.

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Decreased GCF DEL-1 and increased GCF neutrophils with increasing probing pocket depth

  • Seong-Ho Jin;Eun-Mi Lee;Jun-Beom Park;Youngkyung Ko
    • Journal of Periodontal and Implant Science
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    • 제54권2호
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    • pp.85-95
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    • 2024
  • Purpose: Developmental endothelial locus-1 (DEL-1) plays a role in regulating neutrophil migration within the periodontium. The objective of this study was to evaluate the levels of DEL-1 in saliva and gingival crevicular fluid (GCF), as well as the number of neutrophils in patients with periodontitis. Methods: Forty systemically healthy, non-smoking periodontitis patients participated in this study. Clinical periodontal parameters, including the plaque index, probing pocket depth (PPD), clinical attachment level, bleeding on probing, modified sulcular bleeding index, and marginal bone level, were measured. Levels of DEL-1, interleukin (IL)-1β, IL-6, and IL-8 in unstimulated saliva samples, as well as DEL-1 in the GCF of 3 teeth from each participant, were assessed. Neutrophil counts in oral rinse and GCF samples were recorded. Spearman correlation coefficients were used to examine the correlation between protein levels, clinical parameters, and neutrophil quantities. Participants were divided into 2 age groups (those under 50 years and those 50 years or older) in order to investigate potential age-related differences. Results: DEL-1 levels in the GCF showed a negative relationship with PPD (sum). Neutrophils in oral rinse samples were positively correlated with PPD, IL-8, and IL-1β levels. Neutrophils in GCF exhibited a positive correlation with PPD (sum). Salivary DEL-1 levels showed correlations with IL-8 and IL-1β, but not with the clinical parameters of periodontitis. Conclusions: The negative relationship observed between PPD and GCF DEL-1 levels is consistent with the proposed protective role of DEL-1.

Transepithelial Migration of Neutrophils in Response to Leukotriene $B_4$ is Mediated by a Reactive Oxygen Species-ERK-linked Cascade

  • Woo, Chang-Hoon;Kim, Jae-Hong
    • 대한약학회:학술대회논문집
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    • 대한약학회 2003년도 Proceedings of the Convention of the Pharmaceutical Society of Korea Vol.1
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    • pp.103-106
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    • 2003
  • The epithelial cells that form a barrier lining the lung airway are key regulators of neutrophil trafficking into the airway lumen in a variety of lung inflammatory diseases. Although the lipid mediator leukotriene B$_4$ (LTB$_4$) is known to be a principal chemoattractant for recruiting neutrophils to inflamed sites across the airway epithelium, the precise signaling mechanism involved remains largely unknown. (omitted)

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Development of a three-dimensional dynamic model for chemotaxis

  • Song, Jihwan;Kim, Dongchoul
    • Interaction and multiscale mechanics
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    • 제4권2호
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    • pp.165-171
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    • 2011
  • In this study, we proposed a three-dimensional dynamic model under the diffuse interface description for the single crawling cell. From the developed model, we described the clear evolution processes for crawling neutrophil and assessed the reliable quantitative chemotactic property, which confirmed the high possibility of adequate predictions. To establish the system considering of multiple mechanisms such as, diffusion, chemotaxis, and interaction with surface, a diffuse interface model is employed.

Chemotactic Effect of Leukotactin-1/CCL15 on Human Neutrophils

  • Lee Ji-Sook;Yang Eun-Ju;Ryang Yong-Suk;Kim In-Sik
    • 대한의생명과학회지
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    • 제12권3호
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    • pp.145-151
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    • 2006
  • Leukotactin-l (Lkn-l )/CCL15 has been known as a potent chemoattractant of leukocytes. However, the precise function of Lkn-l in human neutrophils has not been explained well. In the present study, we investigated the contribution of Lkn-1 in chemotactic activity of human neutrophils. Both CCR1 and CCR3 mRNA expressions are strongly expressed in human neutrophils but CCR2 protein expression was uniquely detected on the cell surface. Lkn-l binding to CCR1 and CCR3 induced chemotactic activity of neutrophils. Chemotactic index of Lkn-l was comparable to that of IL-8. $MIP-1{\alpha}/CCL3$ binding to CCR1 and CCR5 has no effect on neutrophil migration. Cell migration, in response to Lkn-l, was blocked by pertussis toxin (Ptx), a $G_o/G_i$ protein inhibitor, and U73122, a phospholipase C(PLC) inhibitor but not by protein kinase C inhibitor such as rottlerin, and Ro-31-8425. Taken together, our results demonstrate that Lkn-l transduces the chemotaxis signal through $G_o/G_i$ protein and PLC. This finding provides the molecular mechanism by which Lkn-l may contribute to neutrophil movement into the site of inflammation.

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