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培养的背根神经节中对缓激肽有反应的细胞:细胞大小、放电、胞质钙和P物质

Bradykinin-responsive cells of dorsal root ganglia in culture: cell size, firing, cytosolic calcium, and substance P.

作者信息

Kano M, Kawakami T, Hikawa N, Hori H, Takenaka T, Gotoh H

机构信息

Laboratory for Photobiology, Institute for Physical and Chemical Research (RIKEN), Miyagi, Japan.

出版信息

Cell Mol Neurobiol. 1994 Feb;14(1):49-57. doi: 10.1007/BF02088588.

Abstract
  1. We analyze bradykinin-sensitive cells of the mouse dorsal root ganglion in culture from the viewpoints of cell size, electrical responses, and Ca2+ concentration change due to bradykinin and immunocytochemistry of substance P. 2. Sixteen percent of cells in the cell group 26-30 microns in diameter fired in response to 10 microM bradykinin. None of other cell groups showed a firing response to bradykinin. 3. We measured a cytosolic Ca2+ change due to bradykinin using a Ca(2+)-sensitive fluorescent dye, Fura 2. The rapid rise (peak time, 20 sec) in the Ca2+ concentration was ascribed to Ca2+ release from intracellular Ca2+ stores. The profound change in the Ca2+ concentration was observed again in the cell group 26-30 microns in diameter. Seventeen percent of cells in this group increased the Ca2+ concentration by approximately seven times that at resting level. 4. Among cells which increase Ca2+ concentration responding to bradykinin, 83% of them contain substance P (an immunocytochemical study). 5. We conclude that 16-17% of the cell group 26-30 microns in diameter of the dorsal root ganglia in culture are polymodal nociceptors and respond to bradykinin.
摘要
  1. 我们从细胞大小、电反应、缓激肽引起的钙离子浓度变化以及P物质的免疫细胞化学等方面,对培养的小鼠背根神经节中对缓激肽敏感的细胞进行了分析。2. 直径为26 - 30微米的细胞组中,16%的细胞对10微摩尔缓激肽有放电反应。其他细胞组均未显示出对缓激肽的放电反应。3. 我们使用钙敏荧光染料Fura 2测量了缓激肽引起的胞质钙离子变化。钙离子浓度的快速上升(峰值时间为20秒)归因于细胞内钙库释放钙离子。在直径为26 - 30微米的细胞组中再次观察到钙离子浓度的显著变化。该组中17%的细胞将钙离子浓度提高到约为静息水平的7倍。4. 在对缓激肽有反应且钙离子浓度升高的细胞中,83%含有P物质(免疫细胞化学研究)。5. 我们得出结论,培养的背根神经节中直径为26 - 30微米的细胞组中,16 - 17%是多模式伤害感受器,对缓激肽有反应。

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