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      KCI등재 SCI SCIE SCOPUS

      Plasmodium falciparum Cultivation Using the Petri Dish: Revisiting the Effect of the ‘Age' of Erythrocytes and the Interval of Medium Change

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      https://www.riss.kr/link?id=A104792599

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      Differences in the characteristics of the culture conditions can influence the multiplication rate of Plasmodium falciparum. The Petri dish method is one of the most popular methods of cultivating this parasite. In many previous studies, ideal culture conditions of the Petri dish method were achieved by using erythrocytes collected from blood that had been stored for at least 2 weeks, with daily changes of the medium. In the present study, we studied the multiplication rate of P. falciparum in cultures containing erythrocytes of various ages together with changing the medium at various intervals of time. Our results strongly suggest that the rate of in vitro multiplication of P. falciparum was higher in freshly collected erythrocytes than in aged erythrocytes regardless of the anticoagulant and that when the parasitemia is lower than 8% with a hematocrit of 5%, the medium change interval can be as long as 48 hr without a great reduction in the rate of multiplication.
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      Differences in the characteristics of the culture conditions can influence the multiplication rate of Plasmodium falciparum. The Petri dish method is one of the most popular methods of cultivating this parasite. In many previous studies, ideal culture...

      Differences in the characteristics of the culture conditions can influence the multiplication rate of Plasmodium falciparum. The Petri dish method is one of the most popular methods of cultivating this parasite. In many previous studies, ideal culture conditions of the Petri dish method were achieved by using erythrocytes collected from blood that had been stored for at least 2 weeks, with daily changes of the medium. In the present study, we studied the multiplication rate of P. falciparum in cultures containing erythrocytes of various ages together with changing the medium at various intervals of time. Our results strongly suggest that the rate of in vitro multiplication of P. falciparum was higher in freshly collected erythrocytes than in aged erythrocytes regardless of the anticoagulant and that when the parasitemia is lower than 8% with a hematocrit of 5%, the medium change interval can be as long as 48 hr without a great reduction in the rate of multiplication.

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      참고문헌 (Reference)

      1 "Time course of in vitro maturation of intra-erythrocytic malaria parasite:a comparison between Plasmodium falciparum and Plasmodium knowlesi" 97 : 901-903, 2002

      2 "The economic and social burden of malaria" 415 : 680-685, 2002

      3 "Preferential invasion of malarial merozoites into young red blood cells" 16 : 299-312, 1990

      4 "Plasmodium falciparum:mic-roaerophilic requirements in human red blood cells" 47 : 410-8, Parasitol1979

      5 "Plasmodium falciparum in culture:use of out-dated erythrocytes and description of the candle jar method" 63 : 883-6, 1977

      6 "Invasion and growth of Plasmodium falciparum in different types of human erythrocyte" 55 : 179-86, 1977

      7 "In vitro cultivation of malaria parasites Principle andPractice of Malariology" Churchill Livingstone 307-20, 1988

      8 "Human malaria parasites in continuous cul-ture" 193 : 673-5, 1976

      9 "Gametocytogenesis induction by ammoni-um compounds in cultured Plasmodium falciparum" 20 : 615-8, Parasitol1990

      10 "Cytotoxicity analysis of EDTA and citric acid applied on murine resident macrophage culture" 40 : 338-343, 2007

      1 "Time course of in vitro maturation of intra-erythrocytic malaria parasite:a comparison between Plasmodium falciparum and Plasmodium knowlesi" 97 : 901-903, 2002

      2 "The economic and social burden of malaria" 415 : 680-685, 2002

      3 "Preferential invasion of malarial merozoites into young red blood cells" 16 : 299-312, 1990

      4 "Plasmodium falciparum:mic-roaerophilic requirements in human red blood cells" 47 : 410-8, Parasitol1979

      5 "Plasmodium falciparum in culture:use of out-dated erythrocytes and description of the candle jar method" 63 : 883-6, 1977

      6 "Invasion and growth of Plasmodium falciparum in different types of human erythrocyte" 55 : 179-86, 1977

      7 "In vitro cultivation of malaria parasites Principle andPractice of Malariology" Churchill Livingstone 307-20, 1988

      8 "Human malaria parasites in continuous cul-ture" 193 : 673-5, 1976

      9 "Gametocytogenesis induction by ammoni-um compounds in cultured Plasmodium falciparum" 20 : 615-8, Parasitol1990

      10 "Cytotoxicity analysis of EDTA and citric acid applied on murine resident macrophage culture" 40 : 338-343, 2007

      11 "Culturing oferythrocytic stages of Plasmodium falciparum parasites" Manassas: Va 1-7, 2000

      12 "Culture of humanmalaria parasites" 767-9, nature1976

      13 "Cultivation of malaria parasites" 273 : 621-2, 1978

      14 "Cultivation of malaria parasites" 45 : 7-26, 1994

      15 "Cultivation of Plasmodium spp" 15 : 355-364, 2002

      16 "Cellular basis of early cytokine res-ponse to Plasmodium falciparum" 69 : 2364-2371, 2001

      17 "An improved technique forthe cultivation of Plasmodium falciparum in vitro without daily medi-um change" 79 : 379-84, 1985

      18 "A comparison of static thin layer and suspension cul-tures for the maintenance in vitro of Plasmodium falciparum" 75 : 7-17, 1981

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      학술지 이력

      학술지 이력
      연월일 이력구분 이력상세 등재구분
      2023 평가예정 해외DB학술지평가 신청대상 (해외등재 학술지 평가)
      2020-01-01 평가 등재학술지 유지 (해외등재 학술지 평가) KCI등재
      2011-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2009-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2005-01-01 평가 SCI 등재 (등재유지) KCI등재
      2002-01-01 평가 등재학술지 선정 (등재후보2차) KCI등재
      1999-07-01 평가 등재후보학술지 선정 (신규평가) KCI등재후보
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      학술지 인용정보

      학술지 인용정보
      기준연도 WOS-KCI 통합IF(2년) KCIF(2년) KCIF(3년)
      2016 1.48 0.37 1.06
      KCIF(4년) KCIF(5년) 중심성지수(3년) 즉시성지수
      0.85 0.75 0.691 0.11
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