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Basic and Clinical Neuroscience، جلد ۱۲، شماره ۲، صفحات ۲۰۵-۲۱۲
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عنوان فارسی |
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چکیده فارسی مقاله |
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کلیدواژههای فارسی مقاله |
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عنوان انگلیسی |
Comparison of Rat Primary Midbrain Neurons Cultured in DMEM/F12 and Neurobasal Mediums |
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چکیده انگلیسی مقاله |
Introduction: Midbrain dopaminergic neurons are involved in various brain functions, including motor behavior, reinforcement, motivation, learning, and cognition. Primary dopaminergic neurons and also several lines of these cells are extensively used in cell culture studies. Primary dopaminergic neurons prepared from rodents have been cultured in both DMEM/F12 and neurobasal mediums in several studies. However, there is no document reporting the comparison of these two mediums. So in this study, we evaluated the neurons and astroglial cells in primary midbrain neurons from rat embryos cultured in DMEM/F12 and neurobasal mediums. Methods: Primary mesencephalon cells were prepared from the E14.5 rat embryo. Then they were seeded in two different mediums ( Dulbecco's Modified Eagle Medium/Nutrient Mixture F-12 [DMEM/F12] and neurobasal). On day 3 and day 5, half of the medium was replaced with a fresh medium. On day 7, β3-tubulin-, GFAP (Glial fibrillary acidic protein)- and Tyrosine Hydroxylase TH-positive cells were characterized as neurons, astrocytes, and dopaminergic neurons, respectively, using immunohistochemistry. Furthermore, the morphology of the cells in both mediums was observed under light microscopy on days 1, 3, and 5. Results: The cells cultured in both mediums were similar under light microscopy regarding the cell number, but in a neurobasal medium, the cells have aggregated and formed clustering structures. Although GFAP-immunoreactive cells were lower in neurobasal compared to DMEM/F12, the number of β3-tubulin- and TH-positive cells in both cultures was the same. Conclusion: This study's findings demonstrated that primary midbrain cells from the E14.5 rat embryo could grow in both DMEM/F12 and neurobasal mediums. Therefore, considering the high price of a neurobasal medium, it can be replaced with DMEM/F12 for culturing primary dopaminergic neurons. |
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کلیدواژههای انگلیسی مقاله |
Dopaminergic neurons, Rat mesencephalon cell culture, B27-supplemented neurobasal, DMEM/F12 medium |
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نویسندگان مقاله |
| Neda Valian Neuroscience Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
| Mansooreh Heravi Neuroscience Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
| Abolhassan Ahmadiani Neuroscience Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
| Leila Dargahi Neuroscience Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
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نشانی اینترنتی |
http://bcn.iums.ac.ir/browse.php?a_code=A-10-1568-1&slc_lang=en&sid=1 |
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کد مقاله (doi) |
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زبان مقاله منتشر شده |
en |
موضوعات مقاله منتشر شده |
Cellular and molecular Neuroscience |
نوع مقاله منتشر شده |
Original |
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