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钠泵在两栖类胚胎神经元分化过程中的作用。

The function of the sodium pump during differentiation of amphibian embryonic neurones.

作者信息

Messenger E A, Warner A E

出版信息

J Physiol. 1979 Jul;292:85-105. doi: 10.1113/jphysiol.1979.sp012840.

Abstract
  1. A method has been developed for studying the differentiation in tissue culture of ectoderm and mesoderm derivatives, dissected from amphibian embryos which have just completed neurulation. 2. Neurones, striated muscle cells and pigment cells, together with other unidentifiable cell types, differentiated as a monolayer with approximately the same time course as in the whole embryo. The proportion of different cell types in the cultures was measured quantitatively by cell counting. 3. Treatment of embryos during neurulation with the cardiac glycoside strophanthidin reduced the number of neurones which subsequently differentiated in culture. Other cell types were not affected. 4. The relationship between inhibition of neural differentiation and strophanthidin concentration was sigmoid, with maximum inhibition at 10(-5) M-strophanthidin and the mid-point at 5 X 10(-7) M-strophanthidin. 35% of neurones differentiating in culture were not affected by glycoside treatment. 5. The glycoside hexahydroscillaren A had no effect on neural differentiation. 6. Increasing extracellular potassium to 100 nM during strophanthidin treatment completely protected differentiating neurones from the inhibitory effect of strophanthidin. 7. Treatment of embryos with 100 mM-KCl during neurulation had no effect on the subsequent differentiation of neurones. 8. Treatment of cultures with an antibody to mouse salivary gland Nerve Growth Factor reduced the number of neurones by 30%. 9. Exposure to strophanthidin while the embryo moved from the early neural fold stage to the late neural fold stage was as effective in reducing subsequent neural differentiation as treatment throughout neurulation. 10. The proportion of nerve cells in the cultures was not affected if strophanthidin treatment ended before the early neural fold stage or did not begin until the late neural fold stage. 11. Embryos treated with strophanthidin during neurulation and then allowed to grow into tadpoles developed abnormal nervous systems. 10(-6) M-strophanthidin had little effect on the volume of grey matter, but reduced the white matter by 50%. 12. The results are consistent with the view that strophanthidin achieves its effect on neural differentiation by inhibiting the sodium pump. They are discussed in the light of the suggestion that activation of the sodium pump is an essential part of nerual differentiation.
摘要
  1. 已开发出一种方法,用于研究从刚完成神经胚形成的两栖类胚胎中分离出的外胚层和中胚层衍生物在组织培养中的分化情况。2. 神经元、横纹肌细胞和色素细胞,以及其他无法识别的细胞类型,以单层形式分化,其时间进程与整个胚胎中大致相同。通过细胞计数对培养物中不同细胞类型的比例进行了定量测定。3. 在神经胚形成期间用强心苷毒毛花苷处理胚胎,会减少随后在培养中分化的神经元数量。其他细胞类型未受影响。4. 神经分化抑制与毒毛花苷浓度之间的关系呈S形,在10⁻⁵ M毒毛花苷时抑制作用最大,中点浓度为5×10⁻⁷ M毒毛花苷。在培养中分化的神经元中有35%不受糖苷处理的影响。5. 糖苷六氢洋地黄毒苷A对神经分化没有影响。6. 在毒毛花苷处理期间将细胞外钾离子浓度提高到100 nM,可完全保护分化中的神经元免受毒毛花苷的抑制作用。7. 在神经胚形成期间用100 mM - KCl处理胚胎,对随后神经元的分化没有影响。8. 用抗小鼠唾液腺神经生长因子的抗体处理培养物,可使神经元数量减少30%。9. 当胚胎从早期神经褶阶段发育到晚期神经褶阶段时暴露于毒毛花苷,在减少随后的神经分化方面与在整个神经胚形成期间进行处理一样有效。10. 如果毒毛花苷处理在早期神经褶阶段之前结束或直到晚期神经褶阶段才开始,则培养物中神经细胞的比例不受影响。11. 在神经胚形成期间用毒毛花苷处理的胚胎,然后让其发育成蝌蚪,会发育出异常的神经系统。10⁻⁶ M毒毛花苷对灰质体积影响不大,但使白质减少了50%。12. 这些结果与毒毛花苷通过抑制钠泵对神经分化产生作用的观点一致。根据钠泵激活是神经分化的一个重要部分这一观点对结果进行了讨论。
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e817/1280847/dd5f1dd69a50/jphysiol00869-0112-a.jpg

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