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      KCI등재 SCIE SCOPUS

      Comparative Metabolic Analysis of Lactate for CHO Cells in Glucose and Galactose

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      https://www.riss.kr/link?id=A103818712

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      다국어 초록 (Multilingual Abstract)

      t-PA producing CHO cells have been shown to undergo a metabolic shift when the culture medium is supplemented with a mixture of glucose and galactose. This metabolic change is characterized by the reincorporation of lactate and its use as an additional carbon source. The aim of this work is to understand lactate metabolism. To do so,Chinese hamster ovary cells were grown in batch cultures in four different conditions consisting in different combinations of glucose and galactose. In experiments supplemented with glucose, only lactate production was observed.
      Cultures with glucose and galactose consumed glucose first and produced lactate at the same time, after glucose depletion galactose consumption began and lactate uptake was observed. Comparison of the metabolic state of cells with and without the shift by metabolic flux analysis show that the metabolic fluxes distribution changes mostly in the reactions involving pyruvate metabolism. When not enough pyruvate is being produced for cells to support their energy requirements, lactate dehydrogenase complex changes the direction of the reaction yielding pyruvate to feed the TCA cycle. The slow change from high fluxes during glucose consumption to low fluxes in galactose consumption generates intracellular conditions that allow the influx of lactate.
      Lactate consumption is possible in cell cultures supplemented with glucose and galactose due to the low rates at which galactose is consumed. Evidence suggests that an excessive production and accumulation of pyruvate during glucose consumption leads to lactate production and accumulation inside the cell. Other internal conditions such as a decrease in internal pH, forces the flow of lactate outside the cell. After metabolic shift the intracellular pool of pyruvate, lactate and H+ drops permitting the reversal of the monocarboxylate transporter direction, therefore leading to lactate uptake. Metabolic analysis comparing glucose and galactose consumption indicates that after metabolic shift not enough pyruvate is produced to supply energy metabolism and lactate is used for pyruvate synthesis. In addition, MFA indicates that most carbon consumed during low carbon flux is directed towards maintaining energy metabolism.
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      t-PA producing CHO cells have been shown to undergo a metabolic shift when the culture medium is supplemented with a mixture of glucose and galactose. This metabolic change is characterized by the reincorporation of lactate and its use as an additiona...

      t-PA producing CHO cells have been shown to undergo a metabolic shift when the culture medium is supplemented with a mixture of glucose and galactose. This metabolic change is characterized by the reincorporation of lactate and its use as an additional carbon source. The aim of this work is to understand lactate metabolism. To do so,Chinese hamster ovary cells were grown in batch cultures in four different conditions consisting in different combinations of glucose and galactose. In experiments supplemented with glucose, only lactate production was observed.
      Cultures with glucose and galactose consumed glucose first and produced lactate at the same time, after glucose depletion galactose consumption began and lactate uptake was observed. Comparison of the metabolic state of cells with and without the shift by metabolic flux analysis show that the metabolic fluxes distribution changes mostly in the reactions involving pyruvate metabolism. When not enough pyruvate is being produced for cells to support their energy requirements, lactate dehydrogenase complex changes the direction of the reaction yielding pyruvate to feed the TCA cycle. The slow change from high fluxes during glucose consumption to low fluxes in galactose consumption generates intracellular conditions that allow the influx of lactate.
      Lactate consumption is possible in cell cultures supplemented with glucose and galactose due to the low rates at which galactose is consumed. Evidence suggests that an excessive production and accumulation of pyruvate during glucose consumption leads to lactate production and accumulation inside the cell. Other internal conditions such as a decrease in internal pH, forces the flow of lactate outside the cell. After metabolic shift the intracellular pool of pyruvate, lactate and H+ drops permitting the reversal of the monocarboxylate transporter direction, therefore leading to lactate uptake. Metabolic analysis comparing glucose and galactose consumption indicates that after metabolic shift not enough pyruvate is produced to supply energy metabolism and lactate is used for pyruvate synthesis. In addition, MFA indicates that most carbon consumed during low carbon flux is directed towards maintaining energy metabolism.

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      참고문헌 (Reference)

      1 Poole, R. C, "Transport of lactate and other monocarboxylates across mammalian plasma membranes" 264 : 761-782, 1993

      2 Cheeti, S., "The role of monocarboxylate transporters in uptake of lactic acid in HeLa cells" 325 : 48-54, 2006

      3 Dubinsky, W. P, "The mechanism of lactate transport in human erythrocytes" 44 : 25-36, 1978

      4 Altamirano, C., "Strategies for fed-batch cultivation of t-PA producing CHO cells: Substitution of glucose and glutamine and rational design of culture medium" 110 : 171-179, 2004

      5 Glacken, M. W., "Reduction of waste product excretion via nutrient control: Possible strategies for maximizing product and cell yields on serum in cultures of mammalian cells" 28 : 1376-1389, 1986

      6 Pascoe, D. E., "Proteome analysis of antibody-producing CHO cell lines with different metabolic profiles" 98 : 391-410, 2007

      7 Dawson, A. G., "Oxidation of cytosolic NADH formed during aerobic metabolism in mammalian cells" 4 : 171-176, 1979

      8 Ying, W., "NAD+ and NADH in cellular functions and cell death" 11 : 3129-3148, 2006

      9 Europa, A. F., "Multiple steady states with distinct cellular metabolism in continuous culture of mammalian cells" 67 : 25-34, 2000

      10 Vallino, J. J, "Metabolic flux distributions in Corynebacterium glutamicum during growth and lysine overproduction" 41 : 633-646, 1993

      1 Poole, R. C, "Transport of lactate and other monocarboxylates across mammalian plasma membranes" 264 : 761-782, 1993

      2 Cheeti, S., "The role of monocarboxylate transporters in uptake of lactic acid in HeLa cells" 325 : 48-54, 2006

      3 Dubinsky, W. P, "The mechanism of lactate transport in human erythrocytes" 44 : 25-36, 1978

      4 Altamirano, C., "Strategies for fed-batch cultivation of t-PA producing CHO cells: Substitution of glucose and glutamine and rational design of culture medium" 110 : 171-179, 2004

      5 Glacken, M. W., "Reduction of waste product excretion via nutrient control: Possible strategies for maximizing product and cell yields on serum in cultures of mammalian cells" 28 : 1376-1389, 1986

      6 Pascoe, D. E., "Proteome analysis of antibody-producing CHO cell lines with different metabolic profiles" 98 : 391-410, 2007

      7 Dawson, A. G., "Oxidation of cytosolic NADH formed during aerobic metabolism in mammalian cells" 4 : 171-176, 1979

      8 Ying, W., "NAD+ and NADH in cellular functions and cell death" 11 : 3129-3148, 2006

      9 Europa, A. F., "Multiple steady states with distinct cellular metabolism in continuous culture of mammalian cells" 67 : 25-34, 2000

      10 Vallino, J. J, "Metabolic flux distributions in Corynebacterium glutamicum during growth and lysine overproduction" 41 : 633-646, 1993

      11 Bonarius, H. P., "Metabolic flux analysis of hybridoma cells in different culture media using mass balances" 50 : 299-318, 1996

      12 Zhang, F., "Metabolic characteristics of recombinant Chinese hamster ovary cells expressing glutamine synthetase in presence and absence of glutamine" 51 : 21-28, 2006

      13 Korke, R., "Large scale gene expression profiling of metabolic shift of mammalian cells in culture" 107 : 1-17, 2004

      14 Kurano, N., "Growth behavior of Chinese hamster ovary cells in a compact loop bioreactor: 1. Effects of physical and chemical environments" 15 : 101-111, 1990

      15 Reitzer, L. J., "Evidence that glutamine, not sugar, is the major energy source for cultured HeLa cells" 254 : 2669-2676, 1979

      16 Chen, K., "Engineering of a mammalian cell line for reduction of lactate formation and high monoclonal antibody production" 72 : 55-61, 2001

      17 Cruz, H. J., "Effects of ammonia and lactate on growth, metabolism, and productivity of BHK cells" 27 : 43-52, 2000

      18 Kuwae, S., "Development of a fed-batch culture process for enhanced production of recombinant human antithrombin by Chinese hamster ovary cells" 100 : 502-510, 2005

      19 Lu, S., "Determination of tricarboxylic acid and other related substances in cultured mammalian cells by gradient ion-exchange chromatography with suppressed conductivity detection" 1012 : 161-68, 2003

      20 Bonarius, H. P., "Determination of the respiration quotient in mammalian cell culture in bicarbonate buffered media" 45 : 524-535, 1995

      21 Terada, S., "Cytokines involving gp130 in signal transduction suppressed growth of a mouse hybridoma cell line and enhanced its antibody production" 8 : 889-894, 1996

      22 Altamirano, C., "Considerations on the lactate consumption by CHO cells in the presence of galactose" 125 : 547-556, 2006

      23 Neermann, J, "Comparative analysis of glucose and glutamine metabolism in transformed mammalian cell lines, insect and primary liver cells" 166 : 152-169, 1996

      24 Marquis, C. P., "Carbohydrate and amino acid metabolism during batch culture of a human lymphoblastoid cell line, BTSN6" 21 : 121-132, 1996

      25 Plagemann, P. G., "Broad specificity hexose transport system with differential mobility of loaded and empty carrier, but directional symmetry, is common property of mammalian cell lines" 256 : 2835-2842, 1981

      26 Gambhir, A., "Analysis of cellular metabolism of hybridoma cells at distinct physiological states" 95 : 317-327, 2003

      27 Fussenegger, M., "A novel cytostatic process enhances the productivity of Chinese hamster ovary cells" 55 : 927-939, 1997

      28 Faik, P, "A method for the isolation of Chinese hamster cell variants with an altered ability to utilise carbohydrates" 1 : 555-562, 1977

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      기준연도 WOS-KCI 통합IF(2년) KCIF(2년) KCIF(3년)
      2016 1.14 0.13 0.75
      KCIF(4년) KCIF(5년) 중심성지수(3년) 즉시성지수
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