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      KCI등재 SCIE SCOPUS

      Potential immune-modulatory effects of wheat phytase on the performance of a mouse macrophage cell line, Raw 264.7, exposed to long-chain inorganic polyphosphate

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      https://www.riss.kr/link?id=A107282413

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      다국어 초록 (Multilingual Abstract)

      Objective: This experiment was conducted to find out the immunological effects of wheat phytase when long-chain inorganic polyphosphate (polyP) treated with wheat phytase was added to a macrophage cell line, Raw 264.7, when compared to intact long-chain polyP.
      Methods: Nitric oxide (NO) production of Raw 264.7 cells exposed to P700, a long-chain polyP with an average of 1,150 phosphate residues, treated with or without wheat phytase, was measured by Griess method. Phagocytosis assay of P700 treated with or without phytase in Raw 264.7 cells was investigated using neutral red uptake. The secretion of tumor necrosis factor α (TNF-α) by Raw 264.7 cells with wheat phytase-treated P700 compared to intact P700 was observed by using Mouse TNF-α enzyme-linked immunosorbent assay kit.
      Results: P700 treated with wheat phytase effectively increased NO production of Raw 264.7 cells by 172% when compared with intact P700 at 12 h exposure. At 5 mM of P700 concentration, wheat phytase promoted NO production of macrophages most strongly. P700, treated with wheat phytase, stimulated phagocytosis in macrophages at 12 h exposure by about 1.7-fold compared to intact P700. In addition, P700 treated with wheat phytase effectively increased in vitro phagocytic activity of Raw 264.7 cells at a concentration above 5 mM when compared to intact P700. P700 dephosphorylated by wheat phytase increased the release of TNF-α from Raw 264.7 cells by 143% over that from intact P700 after 6 h exposure. At the concentration of 50 μM P700, wheat phytase increased the secretion of cytokine, TNF-α, by 124% over that from intact P700.
      Conclusion: In animal husbandry, wheat phytase can mitigate the long-chain polyP causing damage by improving the immune capabilities of macrophages in the host. Thus, wheat phytase has potential as an immunological modulator and future feed additive for regulating immune responses caused by inflammation induced by long-chain polyP from bacterial infection.
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      Objective: This experiment was conducted to find out the immunological effects of wheat phytase when long-chain inorganic polyphosphate (polyP) treated with wheat phytase was added to a macrophage cell line, Raw 264.7, when compared to intact long-cha...

      Objective: This experiment was conducted to find out the immunological effects of wheat phytase when long-chain inorganic polyphosphate (polyP) treated with wheat phytase was added to a macrophage cell line, Raw 264.7, when compared to intact long-chain polyP.
      Methods: Nitric oxide (NO) production of Raw 264.7 cells exposed to P700, a long-chain polyP with an average of 1,150 phosphate residues, treated with or without wheat phytase, was measured by Griess method. Phagocytosis assay of P700 treated with or without phytase in Raw 264.7 cells was investigated using neutral red uptake. The secretion of tumor necrosis factor α (TNF-α) by Raw 264.7 cells with wheat phytase-treated P700 compared to intact P700 was observed by using Mouse TNF-α enzyme-linked immunosorbent assay kit.
      Results: P700 treated with wheat phytase effectively increased NO production of Raw 264.7 cells by 172% when compared with intact P700 at 12 h exposure. At 5 mM of P700 concentration, wheat phytase promoted NO production of macrophages most strongly. P700, treated with wheat phytase, stimulated phagocytosis in macrophages at 12 h exposure by about 1.7-fold compared to intact P700. In addition, P700 treated with wheat phytase effectively increased in vitro phagocytic activity of Raw 264.7 cells at a concentration above 5 mM when compared to intact P700. P700 dephosphorylated by wheat phytase increased the release of TNF-α from Raw 264.7 cells by 143% over that from intact P700 after 6 h exposure. At the concentration of 50 μM P700, wheat phytase increased the secretion of cytokine, TNF-α, by 124% over that from intact P700.
      Conclusion: In animal husbandry, wheat phytase can mitigate the long-chain polyP causing damage by improving the immune capabilities of macrophages in the host. Thus, wheat phytase has potential as an immunological modulator and future feed additive for regulating immune responses caused by inflammation induced by long-chain polyP from bacterial infection.

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      다국어 초록 (Multilingual Abstract)

      Objective: This experiment was conducted to find out the immunological effects of wheat phytase when long-chain inorganic polyphosphate (polyP) treated with wheat phytase was added to a macrophage cell line, Raw 264.7, when compared to intact long-chain polyP.Methods: Nitric oxide (NO) production of Raw 264.7 cells exposed to P700, a long-chain polyP with an average of 1,150 phosphate residues, treated with or without wheat phytase, was measured by Griess method. Phagocytosis assay of P700 treated with or without phytase in Raw 264.7 cells was investigated using neutral red uptake. The secretion of tumor necrosis factor α (TNF-α) by Raw 264.7 cells with wheat phytase-treated P700 compared to intact P700 was observed by using Mouse TNF-α enzyme-linked immunosorbent assay kit.Results: P700 treated with wheat phytase effectively increased NO production of Raw 264.7 cells by 172% when compared with intact P700 at 12 h exposure. At 5 mM of P700 concentration, wheat phytase promoted NO production of macrophages most strongly. P700, treated with wheat phytase, stimulated phagocytosis in macrophages at 12 h exposure by about 1.7-fold compared to intact P700. In addition, P700 treated with wheat phytase effectively increased <i>in vitro</i> phagocytic activity of Raw 264.7 cells at a concentration above 5 mM when compared to intact P700. P700 dephosphorylated by wheat phytase increased the release of TNF-α from Raw 264.7 cells by 143% over that from intact P700 after 6 h exposure. At the concentration of 50 μM P700, wheat phytase increased the secretion of cytokine, TNF-α, by 124% over that from intact P700.Conclusion: In animal husbandry, wheat phytase can mitigate the long-chain polyP causing damage by improving the immune capabilities of macrophages in the host. Thus, wheat phytase has potential as an immunological modulator and future feed additive for regulating immune responses caused by inflammation induced by long-chain polyP from bacterial infection.
      번역하기

      Objective: This experiment was conducted to find out the immunological effects of wheat phytase when long-chain inorganic polyphosphate (polyP) treated with wheat phytase was added to a macrophage cell line, Raw 264.7, when compared to intact long-cha...

      Objective: This experiment was conducted to find out the immunological effects of wheat phytase when long-chain inorganic polyphosphate (polyP) treated with wheat phytase was added to a macrophage cell line, Raw 264.7, when compared to intact long-chain polyP.Methods: Nitric oxide (NO) production of Raw 264.7 cells exposed to P700, a long-chain polyP with an average of 1,150 phosphate residues, treated with or without wheat phytase, was measured by Griess method. Phagocytosis assay of P700 treated with or without phytase in Raw 264.7 cells was investigated using neutral red uptake. The secretion of tumor necrosis factor α (TNF-α) by Raw 264.7 cells with wheat phytase-treated P700 compared to intact P700 was observed by using Mouse TNF-α enzyme-linked immunosorbent assay kit.Results: P700 treated with wheat phytase effectively increased NO production of Raw 264.7 cells by 172% when compared with intact P700 at 12 h exposure. At 5 mM of P700 concentration, wheat phytase promoted NO production of macrophages most strongly. P700, treated with wheat phytase, stimulated phagocytosis in macrophages at 12 h exposure by about 1.7-fold compared to intact P700. In addition, P700 treated with wheat phytase effectively increased <i>in vitro</i> phagocytic activity of Raw 264.7 cells at a concentration above 5 mM when compared to intact P700. P700 dephosphorylated by wheat phytase increased the release of TNF-α from Raw 264.7 cells by 143% over that from intact P700 after 6 h exposure. At the concentration of 50 μM P700, wheat phytase increased the secretion of cytokine, TNF-α, by 124% over that from intact P700.Conclusion: In animal husbandry, wheat phytase can mitigate the long-chain polyP causing damage by improving the immune capabilities of macrophages in the host. Thus, wheat phytase has potential as an immunological modulator and future feed additive for regulating immune responses caused by inflammation induced by long-chain polyP from bacterial infection.

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      참고문헌 (Reference)

      1 Dionisio G, "Wheat(Triticum aestivum L. )and barley(Hordeum vulgare L. )multiple inositol polyphosphate phosphatases(MINPPs)are phytases expressed during grain filling and germination" 5 : 325-338, 2007

      2 Zhang W, "Tris(1, 3-dichloro2-propyl)phosphate treatment induces DNA damage, cell cycle arrest and apoptosis in murine RAW264. 7 macrophages" 44 : 133-144, 2019

      3 Brown MRW, "The long and short of it-polyphosphate, PPK and bacterial survival" 33 : 284-290, 2008

      4 Yang J, "Sphingosine 1-phosphate(S1P)/S1P receptor2/3 axis promotes inflammatory M1polarization of bone marrow-derived monocyte/macrophage via G(α)i/o/PI3K/JNK pathway" 49 : 1677-1693, 2018

      5 Yan F, "Probiotics and immune health" 27 : 496-501, 2011

      6 Kumar A, "Polyphosphate and associated enzymes as global regulators of stress response and virulence in Campylobacter jejuni" 22 : 7402-7414, 2016

      7 Dinarvand P, "Polyphosphate amplifies proinflammatory responses of nuclear proteins through interaction with receptor for advanced glycation end products and P2Y1 purinergic receptor" 123 : 935-945, 2014

      8 Dersjant-Li Y, "Phytase in non-ruminant animal nutrition : a critical review on phytase activities in the gastrointestinal tract and influencing factors" 95 : 878-896, 2015

      9 Zhao J, "PTPRO exaggerates inflammation in ulcerative colitis through TLR4/NF-κB pathway" 121 : 1061-1071, 2020

      10 Yang L, "PTP1B promotes macrophage activation by regulating the NF-κB pathway in alcoholic liver injury" 319 : 11-21, 2020

      1 Dionisio G, "Wheat(Triticum aestivum L. )and barley(Hordeum vulgare L. )multiple inositol polyphosphate phosphatases(MINPPs)are phytases expressed during grain filling and germination" 5 : 325-338, 2007

      2 Zhang W, "Tris(1, 3-dichloro2-propyl)phosphate treatment induces DNA damage, cell cycle arrest and apoptosis in murine RAW264. 7 macrophages" 44 : 133-144, 2019

      3 Brown MRW, "The long and short of it-polyphosphate, PPK and bacterial survival" 33 : 284-290, 2008

      4 Yang J, "Sphingosine 1-phosphate(S1P)/S1P receptor2/3 axis promotes inflammatory M1polarization of bone marrow-derived monocyte/macrophage via G(α)i/o/PI3K/JNK pathway" 49 : 1677-1693, 2018

      5 Yan F, "Probiotics and immune health" 27 : 496-501, 2011

      6 Kumar A, "Polyphosphate and associated enzymes as global regulators of stress response and virulence in Campylobacter jejuni" 22 : 7402-7414, 2016

      7 Dinarvand P, "Polyphosphate amplifies proinflammatory responses of nuclear proteins through interaction with receptor for advanced glycation end products and P2Y1 purinergic receptor" 123 : 935-945, 2014

      8 Dersjant-Li Y, "Phytase in non-ruminant animal nutrition : a critical review on phytase activities in the gastrointestinal tract and influencing factors" 95 : 878-896, 2015

      9 Zhao J, "PTPRO exaggerates inflammation in ulcerative colitis through TLR4/NF-κB pathway" 121 : 1061-1071, 2020

      10 Yang L, "PTP1B promotes macrophage activation by regulating the NF-κB pathway in alcoholic liver injury" 319 : 11-21, 2020

      11 Corr EM, "Osteoarthritis-associated basic calcium phosphate crystals activate membrane proximal kinases in human innate immune cells" 19 : 23-, 2017

      12 Lorenz B, "Mammalian intestinal alkaline phosphatase acts as highly active exopolyphosphatase" 1547 : 254-261, 2001

      13 Song G, "Isolation of a polysaccharide with anticancer activity from Auricularia polytricha using high-speed countercurrent chromatography with an aqueous two-phase system" 1217 : 5930-5934, 2010

      14 Kim KS, "Inorganic polyphosphate is essential for long-term survival and virulence factors in Shigella and Salmonella spp" 99 : 7675-7680, 2002

      15 Varas MA, "Inorganic polyphosphate is essential for Salmonella Typhimurium virulence and survival in Dictyostelium discoideum" 8 : 8-, 2018

      16 Brown MRW, "Inorganic polyphosphate in the origin and survival of species" 101 : 16085-16087, 2004

      17 Hassanian SM, "Inorganic polyphosphate elicits pro-inflammatory responses through activation of the mammalian target of rapamycin complexes 1 and 2 in vascular endothelial cells" 13 : 860-871, 2015

      18 Hassanian SM, "Inorganic polyphosphate : a key modulator of inflammation" 15 : 213-218, 2017

      19 Delcenserie V, "Immunomodulatory effects of probiotics in the intestinal tract" 10 : 37-54, 2008

      20 Zhu J, "Immunomodulatory effects of novel bifidobacterium and lactobacillus strains on murine macrophage cells" 5 : 8-15, 2011

      21 Liu CF, "Immunomodulatory and antioxidant potential of Lactobacillus exopolysaccharides" 91 : 2284-2291, 2011

      22 Triantafillidis JK, "Favorable results from the use of herbal and plant products in inflammatory bowel disease : evidence from experimental animal studies" 29 : 268-281, 2016

      23 Liu N, "Effects of phytate and phytase on the performance and immune function of broilers fed nutritionally marginal diets" 87 : 1105-1111, 2008

      24 Mizumachi K, "Effect of fermented liquid diet prepared with Lactobacillus plantarum LQ80 on the immune response in weaning pigs" 3 : 670-676, 2009

      25 Morita H, "Cytokine production by the murine macrophage cell line J774. 1 after exposure to lactobacilli" 66 : 1963-1966, 2002

      26 Kilaparty SP, "Computational analysis reveals a successive adaptation of multiple inositol polyphosphate phosphatase 1 in higher organisms through evolution" 10 : 239-250, 2014

      27 Jeongmin An, "Catalytic properties of wheat phytase that favorably degrades long-chain inorganic polyphosphate" 아세아·태평양축산학회 33 (33): 127-131, 2020

      28 Pokhrel A, "Assaying for inorganic polyphosphate in bacteria" 143 : e58818-, 2019

      29 Klimp AH, "A potential role of macrophage activation in the treatment of cancer" 44 : 143-161, 2002

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      연월일 이력구분 이력상세 등재구분
      2023 평가예정 해외DB학술지평가 신청대상 (해외등재 학술지 평가)
      2021-01-01 학술지명변경 한글명 : ASIAN-AUSTRALASIAN JOURNAL OF ANIMAL SCIENCES -> Animal Bioscience
      외국어명 : ASIAN-AUSTRALASIAN JOURNAL OF ANIMAL SCIENCES -> Animal Bioscience
      KCI등재
      2020-01-01 평가 등재학술지 유지 (해외등재 학술지 평가) KCI등재
      2013-10-01 평가 SCI 등재 (등재유지) KCI등재
      2013-10-01 평가 SCOPUS 등재 (등재유지) KCI등재
      2012-01-01 평가 등재후보학술지 유지 (기타) KCI등재후보
      2011-01-01 평가 등재후보 1차 PASS (등재후보1차) KCI등재후보
      2009-12-29 학회명변경 한글명 : 아세아ㆍ태평양축산학회 -> 아세아·태평양축산학회 KCI등재후보
      2005-09-28 학술지명변경 한글명 : 아세아태평양축산학회지 -> ASIAN-AUSTRALASIAN JOURNAL OF ANIMAL SCIENCES KCI등재후보
      2003-01-01 평가 SCIE 등재 (신규평가) KCI등재후보
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      기준연도 WOS-KCI 통합IF(2년) KCIF(2년) KCIF(3년)
      2016 1.03 0.23 0.76
      KCIF(4년) KCIF(5년) 중심성지수(3년) 즉시성지수
      0.6 0.5 0.367 0.04
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