P-98: The Effect of Primary pH Values of Medium Culture on Expression of Human Follicle Stimulating Hormone in Recombinant Chinese Hamster Ovary Cells.

نویسندگان

  • A Amiri Yekta Department of Genetics, Reproductive Biomedicine Research Centre, Royan Institute for Reproductive Biomedicine, ACECR, Tehran, Iran
  • B Abd Emami Department of Genetics, Reproductive Biomedicine Research Centre, Royan Institute for Reproductive Biomedicine, ACECR, Tehran, Iran���
  • F Tabande Department of Medical Biotechnology, National Institute of Genetic Engineering and Biotechnology (NIGEB), Tehran, Iran
  • M Gharanfoli Department of Molecular and Cellular Biology, University of Science and Culture, ACECR, Tehran, Iran
  • M Qafary Department of Genetics, Reproductive Biomedicine Research Centre, Royan Institute for Reproductive Biomedicine, ACECR, Tehran, Iran
  • MH Sanati Department of Genetics, Reproductive Biomedicine Research Centre, Royan Institute for Reproductive Biomedicine, ACECR, Tehran, Iran
  • N Fatemi Department of Genetics, Reproductive Biomedicine Research Centre, Royan Institute for Reproductive Biomedicine, ACECR, Tehran, Iran���
  • SM Qafari Department of Medical Biotechnology, National Institute of Genetic Engineering and Biotechnology (NIGEB), Tehran, Iran
چکیده مقاله:

Background One of the common gonadotropin hormones used for infertility treatment is recombinant Follicle stimulating hormone (rFSH). pH is an environmental factor that can affect production of recombinant proteins with no imposing cost. Culture pH is known as a parameter that significantly affects cell growth and protein production. In this study, tried to investigate the effect of different pH values on cells growth and rFSH production.�� MaterialsAndMethods The primary pH changes were carried out by adding NaOH and HCL 1 N to medium culture. The range of considered pH values was (6.7-7.6). Trypan blue staining method was applied for cells counting and measuring viability of the cells. Total protein concentration was determined by Bradford assay and Western blotting used for detection of rFSH. qRT-PCR and ImageJ software were used for quantification assays. Results According to obtained data, at the first stationary phase of cells growth, by evaluating the pH values to 7/6, the cells viability, mRNA ratio of rFSH and rFSH production significantly was decreased. The highest cells viability and mRNA ratio of FSH and FSH production were seen in medium with pH=7.0. The achieved results from relative gene expression at pH=6.7 and pH=7.0 didn�t show a significant difference. Conclusion Considering obtained data, by lowering pH value to 7.0 for cells, without any cost, the highest proliferation, will be achieved.

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عنوان ژورنال

دوره 9  شماره 2

صفحات  84- 84

تاریخ انتشار 2015-09-01

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