• Biomolecules & Therapeutics
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• 제1권2호
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• pp.131-136
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• 1993

In the present study, the effect of $HgCl_2$on the function of human peripheral polymorphonuclear leukocytes(PMNs) was examined. PMNs were isolated from human peripheral blood with density centrifugation in Ficoll-Paque. The cells were then incubated with $0.5{\sim}5{\mu}M\;HgCl_2$and glass adherence, chemotactic activity and erythrocyte-antibody rosette forming activity were measured. $HgCl_2$ decreased the function of PMNs in all three aspects tested. $HgCl_2$significantly diminished glass adherence(40.5 {\mu}M: 92{\pm}12%$ (percentage of control, $mean{\pm}$ S.D.); 41 {\mu}M: 46{\pm}11%,$ P<0.01; $3{\mu}M: 35{\pm}7%,$P<0.01;$5{\mu}M:49{\pm}10%,$ P<0.01). Similarly, significant differences were observed in chemotactic activity after $HgCl_2$treatment compared with control (control: $0.95{\pm}0.14mm; 0.5 {\mu}M: 0.91{\pm}0.11 mm; 1 {\mu}M: 0.77{\pm}0.16mm, P<0.05; 3{\mu}M: 0.61{\pm} 0.06mm, P<0.01; 5{\mu}M: 0.15{\pm}0.03 mm, P<0.01).$ Also, 4HgCl_2$decreased the percentage of rosette-forming PMNs, indicating diminished phagocytic activity of PMNs upon $HgCl_2$ exposure compared with control (control: $58{\pm}4%; 1{\mu}M: 53{\pm}4%, p<0.05; 3{\mu}M: 49{\pm}3%, P<0.01; 5{\mu}M: 46{\pm}3%, P<0.01).$ Cell viability was not antered after $HgCl_2$treatment (483{\pm}5%$ viability in control PMNs versus $81{\pm}8%$ viability in $5{\mu}M$ Hg-treated PMNs), suggesting that the impaired PMN function after $HgCl_2$treatment was not due to nonspecific cytotoxicity induced by $HgCl_2$. $HgCl_2$-induced decrease in the function of PMNs may have some implications in depressed host susceptibilityupon bacterial challenge after mercury exposure.

• Current Research on Agriculture and Life Sciences
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• 제11권
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• pp.121-132
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• 1993

대두(大豆)-근류균(根瘤菌)의 공생(共生)에서 숙주식물(宿主植物)의 Root Exudate에 대한 근류균(根瘤菌)의 화학주성(化學走性)이 근류형성(根瘤形性)(숙주식물(宿主植物))에 미치는 영향(影響)을 밝히기 위해 연구(硏究)한 결과(結果)는 다음과 같다. 대두(大豆) Seed Lectin은 품종간(品種間) 차이(差異)가 없었으며 분자량(分子量) 120,000정도(程度)의 4개(個)의 동일(同一)한 subunit를 가지는 물질(物質)이며, Pea Seed Lectin은 분자량(分子量) 44,000정도(程度)이며 15,000과 7,000정도(程度)의 두 종류(種類)의 subunit를 가지는 물질(物質)이며 대두(大豆) lectin은 표준 lectin 항체와 침강선을 형성하였다. 그러나 완두의 lectin은 표준 lectin과 항원-항체반응이 없었으므로 두 lectin은 동일 항원이 되지 않아 서로 다른 물질이었다. 팔달의 Crude Root Exudate에 대(對)한 근류균(根瘤菌)의 화학주성(化學走性) 비(比)는 KCTC 2422는 각각(各各) 3.5이고 LPN-100은 1.4이며 LCR-101은 각각(各各) 1.4이었다. 뿌리분비물의 각 fraction에 대한 근류균의 화학주성은 중성분획이 가장 높고 양성분획이 그다음이며 음성분획이 가장 낮은 화학주성을 나타내어 각물질에 대한 근류균의 친화도에 차이가 있었다. 근류형성(根瘤形性)의 정도(程度)는 KCTC 2422의 경우(境遇)는 접종(接種)후 7日경부터 Nitrogenase Activity가 나타났으며 LCR-101는 15일 이후(以後)에 Nitrogenase Activity를 나타내었다. LPN-100은 Nitrogenase Activity가 전혀 나타나지 않아 근류균(根瘤菌)의 화학주성(化學走性)이 숙주인식과정(宿主認識過程)에 영향(影響)을 미쳤음을 확인(確認)할 수 있었다.

• Journal of Periodontal and Implant Science
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• 제27권4호
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• pp.867-882
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• 1997

Safflower(Carthamus tinctorius $Linn\acute{e}$ has been traditionally used for the treatment of blood stasis, and Dipsasi Radix has been used as a drug for fracture in Chinese medicine. The purpose of present study was to examine the biologic effects of safflower extract and Disasi radix extracts on the periodontal. ligament cells and osteoblastic cells and on the wound healing of rat calvarial defect. The ethanolic extract of safflower blossom, safflower seed and Dipsasi Radix(125, 250, and 500 ${\mu}g/ml$) were prepared as test group, and PDGF-BB(lOng/ml) and unsafonifiable fraction of Zea Mays L.(125, 250, and 500 ${\mu}g/ml$) were employed as positive control. The effects of each agents on the growth and survival, ALPase activity, expression of PDGF-BB receptor, chemotactic response of PDL cell and ATCC human osteosarcoma MG63 cells in vitro were examined. The tissue regenerative effect of each extracts was evaluated by histomorphometric measuring of newly formed bone on the 8mm defect in rat calvaria after oral administration of 3 different dosages groups : 0.02, 0.1 and 0.35g/kg, per day. It was also employed the same dosages of unsaponifiable fraction of Zea Mays L. as positive controls. Safflower blossom extract, safflower seed extract, and Dipsasi Radix extract stimulate the cellular activity of MG63 cells in concentration range of $125-500{\mu}g/ml$, and safflower bolssom extract and safflower seed extract stimulate also the cellular activity of periodontal ligament cells in concentration range of $250-500{\mu}g/ml$. In activity of ALPase, $250-500{\mu}g/ml$ of safflower blossom extracts showed significant stimulating effects on MG63 cells, and the same concentration range of safflower seed extracts showed significant effect on periodontal ligament cells. In the recovery on PDGF-BB receptor expression which was depressed by $IL-1{\beta}$, $125-250{\mu}g/ml$ of safflower blossom extracts and $250-500{\mu}g/ml$ of safflower seed extracts showed significant increasing effect on MG63 cells, and $500{\mu}g/ml$ of safflower blossom extract and $250-500{\mu}g/ml$ of safflower seed extracts showed significant effect on periodontal ligament cells. In chemotactic response, among all tested group, safflower seed extracts only were chemotactic to MG63 cells and periodontal ligament cells in concentration range of $125-500{\mu}g/ml$. Also in the view of bone regeneration in rat calvarial defect model, the only group that was orally administrated 0.35g/kg, day of safflower seed extract showed significant new bone formation. These results suggested that safflower extracts might have a potential possibilities as an useful drug for adjunct to treatment for regeneration of periodontal defect.

• BMB Reports
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• 제35권5호
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• pp.482-487
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• 2002

Early activation of human peripheral blood polymorphonuclear neutrophils is characterized by their morphological changes from spherical to polarized shapes. The endotoxins from enteric pathogens (S. dysenteriae type 1, V. cholerae Inaba 569B, S. typhimurium, and K. pneumoniae) were assessed by their ability to induce morphological polarization of the neutrophils as measures of early activation. Phagocytic activity, adhesion, chemokinetic locomotion, and nitroblue tetrazolium (NBT) dye-reduction ability measured the later activation of the cells. Neutrophils showed distinct morphological polarization in suspension over a wide range of concentrations of these endotoxins when were compared with those that were induced by the standard chemotactic factor, N-formyl-L-methionyl-L-leucyl-L-phenylalanine (FMLP). It was discovered that all of the endotoxins induced locomotor responses in neutrophils in suspension that were dose- and time-dependent. The optimum concentration for the endotoxins of S. dysenteriae, V. cholerae, and K. pneumoniae was 1 mg/ml in which 71, 69, and 66% of the neutrophils were polarized. However, the S. typhimurium dose was 2 mg/ml in which 50% of the cells responded. Neutrophils that were stimulated with endotoxins also showed increased random locomotion (p<0.005) through cellulose nitrate filters, but an enhanced adhesion of the cells to glass surfaces (p<0.03). These are important functions of these cells to reach and phagocytose damaged cells, as well as invading microorganisms. Interestingly, the endotoxins had a highly-significant inhibitory effect upon the proportions of neutrophils phagocytosing opsonized yeast (p<0.01) with a small number of yeast that were engulfed by the cells (p<0.02). Further, endotoxin-treated cells showed an enhanced ability to reduce NBT dye (p<0.03). Therefore, we concluded that endotoxins of enteric pathogens are neutrophil chemotactic factors.

• 한국임상수의학회지
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• 제29권3호
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• pp.207-212
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• 2012

개 말초혈액 다형핵백혈구(PMNs)의 유주활성에 대한 fucoidan의 면역증효과를 검토하였다. Fucoidan 그 자체는 PMNs에 대해 직접적인 유주활성 효과를 보이지 않았다. 그러나 recombinant IL-8에 대한 PMNs의 유주활성과 유사하게 fucoidan으로 배양한 말초혈액 단핵구세포(PBMCs)의 배양상층액은 PMNs에 대해 유주활성을 증가시켰다. 또한, fucoidan으로 배양한 PBMCs의 배양상층액에 대한 PMNs의 유주활성 증가효과는 anti-IL-8 pAb를 처리했을 때 억제되었다. PBMCs 배양 상층액 속의 IL-8의 양을 정량한 결과 fucoidan무처치 대조군에 비해 증가하였다. 이상의 결과로부터, fucoidan은 개 PMNs의 유주능에 대하여 면역증가 작용을 가지고 있으며, 이것은 fucoidan의 자극에 의해 PBMCs에서 생산되어 분비되는 IL-8에 의해 나타나는 것으로 사료되었다.

• 대한약학회:학술대회논문집
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• 대한약학회 2002년도 Proceedings of the Convention of the Pharmaceutical Society of Korea Vol.2
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• pp.305.2-306
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• 2002

In recent studies on cefodizime, it may potentially have the capability of stimulating chemotactic activity of neutrophils and monocytes as well as the strong immuno-modulator. In turn, infection can result in a drastic change of mediators. which lead to initiate an immune response in an indirect way. With this backgrounds, we have studied to see if cefodizime can be a potential substance to induce an immunological function in dendritic cells and peritoneal macrophages. (omitted)

• 한국토양비료학회지
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• 제27권2호
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• pp.136-146
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• 1994

대두 근류균 공생에서 뿌리분비물에 대한 근류균의 화학주성이 근류형성에 미치는 영향을 조사 연구한 결과는 다음과 같다. 2mM proline에 대한 표준균주와 변이주의 화학주성비는 KCTC 2422는 3.1, LPN-100은 1.3, LCR-101은 1.0이었으며 전형적인 Slow growing Rhizobia였다. 팔달 및 백운의 뿌리분비물 추출액에 대한 근류균의 화학주성비는 KCTC 2422는 3.5/3.2 이고 LPN-100은 1.3/1.4이며 LCR-101은 1.4/1.4정도였다. Dowex 칼럼으로부터 용출시킨 Fraction I, II, III에 대한 화학주성비는 Fraction I>II>III순이었고 중성분획인 Glucose와 Ribose, 양성분획인 Aspartic acid와 Glutamine, 음성분획인 Citric acid, Succinic acid에 대한 화학주성비는 공히 $10^{-3}M$일때 가장높은 화학주성비를 나타내었다. 근류형성의 정도는 KCTC 2422는 접종후 7일경부터 Nitrogenase 활성이 나타나기 시작하며 LCR-101은 15일 이후에 Nitrogenase 활성이 나타났으며 LPN-100은 전혀 근류를 형성하지 않아 근류균의 화학주성이 숙주인식의 초기과정에 영향을 미쳤음을 확인할 수 있었다.

• Tuberculosis and Respiratory Diseases
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• 제46권3호
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• pp.338-349
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• 1999

연구배경: 호중구는 급성염증이 있을 때 존재하는 제일 많은 세포로서 폐의 염증이 있을 때에도 말초혈액에서부터 이동됨과 동시에 활성화된 호중구에서 분비하는 단백분해효소, 산화물 및 여러 가지 cytokine등에 의해 염증이 더욱 심해지고 호중구의 이동이 더욱 증가되는 것으로 알려져 있다. 호중구의 이동을 증가시키는 물질로 현재까지 LTB4, PAF, C5a, fMLP, TNF, IL-8 등이 밝혀져 있으며 특히 IL-8은 chemokine이라고 부르는 조그만 cytokine에 속하며 GRO/MGSA는 IL-8과 같은 C-X -C subgroup에 속하는 단백질로서 이 유전인자는 PF-4, IL-8등과 같은 chromosome 4q12-q21에 위치한다. IL-8이 호중구의 이동 및 활성화에 강력한 영향을 미치는 것은 잘 증명되어 있지만 같은 C-X-C subgroup에 속하며 최근에 발견된 GRO/MGSA의 기능 및 발현과정 등에 대해서는 잘 밝혀져 있지 않다. 내피세포는 TNF$\alpha$나 IL-1$\beta$ 등의 자극을 받으면 호중구의 유착을 돕는 접착분자 및 IL-8등의 생성이 증가되는등 염증반응에 능동적인 역할을 한다고 밝혀지고 있다. 저자들은 인체의 제대정맥에서 내피세포를 분리하여 TNF나 IL-1로 자극을 가하였을때 호중구의 이동을 증가시키는 IL-8이나 GRO/MGSA mRNA의 발현과 분비가 일어나는지 또한 호중구 화학주성에 미치는 각각의 기여도를 비교, 관찰하고자 하였다. 방 법: 제대정맥에서 내피세포를 분리, 배양하고 여기에 TNF-$\alpha$ IL-1$\beta$ 등을 0.2, 2, 20 ${\mu}g/ml$ 농도로 자극을 가하고 1, 4, 8, 24 시간이 경과하여 IL-8 및 GRO/MGSA mRNA의 발현을 RT-PCR로 관찰하고, 배양상층액내 IL-8 및 GRO/MGSA의 양을 ELISA로 측정하였으며 상층액의 호종구 화학주성 활성화도를 Neuro Probe 48 well chemotactic chamber를 이용하여 측정하였다. 결 과: 제대정맥 내피세포에 TNF-$\alpha$ 및 IL-1$\beta$로 자극하였을 때 내피세포에서의 IL-8 mRNA는 1 시간후부터, GRO/MGSA mRNA의 발현은 4 시간후부터 각각 관찰되었으며 TNF-$\alpha$ 및 IL-1$\beta$의 자극농도에 따른 뚜렸한 차이는 없었다. TNF-$\alpha$ 및 IL-1$\beta$로 자극한 내피세의 배양상층액에서 측정한 IL-8도 1시간후부터 현저히 증가되었고 GRO/MGSA의 양은 4시간후부터 현저히 증가되어 있었다. TNF-$\alpha$ 및 IL-1$\beta$로 자극한 내피세포의 배양상층액의 호중구 화학주성활성화도는 각각으로 1시간 자극 후에 현저히 증가되어 있었다. 결 론: 이상의 결과에서 제대정맥 내피세포를 TNF-$\alpha$ 및 IL-1$\beta$로 자극시 IL-8 및 GRO/MGSA mRNA 발현 및 단백이 분비되며, 특히 IL-8은 1시간 후에 GRO/MGSA는 4 시간후에 각각 증가되고 호중구화학주성활성화는 1시간후부터 최고치로 증가됨을 관찰하여, GRO/MGSA보다는 IL-8 이 호종구유주인자로서의 중요한 역할을 할것으로 생각된다.

• The Korean Journal of Physiology and Pharmacology
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• 제19권4호
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• pp.327-334
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• 2015

The cytoprotective enzyme heme oxygenase-1 (HO-1) influences endothelial cell survival, proliferation, inflammatory response, and angiogenesis in response to various angiogenic stimuli. In this study, we investigate the involvement of HO-1 in the angiogenic activity of orexin-A. We showed that orexin-A stimulates expression and activity of HO-1 in human umbilical vein endothelial cells (HUVECs). Furthermore, we showed that inhibition of HO-1 by tin (Sn) protoporphryin-IX (SnPP) reduced orexin- A-induced angiogenesis in vivo and ex vivo. Orexin-A-stimulated endothelial tube formation and chemotactic activity were also blocked in SnPP-treated vascular endothelial cells. Orexin-A treatment increased the expression of nuclear factor erythroid-derived 2 related factor 2 (Nrf2), and antioxidant response element (ARE) luciferase activity, leading to induction of HO-1. Collectively, these findings indicate that HO-1 plays a role as an important mediator of orexin-A-induced angiogenesis, and provide new possibilities for therapeutic approaches in pathophysiological conditions associated with angiogenesis.

• BMB Reports
• /
• 제47권11호
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• pp.649-654
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• 2014

Neutrophils play an important role in the initiation of innate immunity against infection and injury. Although many different types of G-protein coupled receptors are functionally expressed in neutrophils, no reports have demonstrated functional expression of umami taste receptor in these cells. We observed that mouse neutrophils express the umami taste receptor T1R1/T1R3 through RNA sequencing and quantitative RT-PCR analysis. Stimulation of mouse neutrophils with L-alanine or L-serine, which are ligands for the umami taste receptor, elicited not only ERK or p38 MAPK phosphorylation but also chemotactic migration. Moreover, addition of L-alanine or L-serine markedly reduced the production of several cytokines including $TNF-{\alpha}$ induced by lipopoly-saccharide (LPS) through inhibition of $NF-{\kappa}B$ activity or STAT3 phosphorylation in neutrophils. Our findings demonstrate that neutrophils express the umami taste receptor, through which tastants stimulate neutrophils, resulting in chemotactic migration, and attenuation of LPS-induced inflammatory response.