Tempia F, Kano M, Schneggenburger R, Schirra C, Garaschuk O, Plant T, Konnerth A
I. Physiologisches Institut, Universität des Saarlandes, Homburg, Germany.
J Neurosci. 1996 Jan 15;16(2):456-66. doi: 10.1523/JNEUROSCI.16-02-00456.1996.
The Ca(2+)-permeation properties of AMPA-receptor (AMPA-R) channels in Purkinje neurons in rat cerebellar slices were studied using a combination of whole-cell patch-clamp recordings, Fura-2 fluorometry, and single-cell reverse-transcription (RT)-PCR. Several lines of evidence indicate that Purkinje neurons, at both early and late stages of postnatal development, express exclusively AMPA-R channels with a low Ca2+ permeability. First, no Ca2+ signal was detected during application of either AMPA or kainate to Purkinje neurons loaded with the Ca2+ indicator Fura-2 AM. In contrast, kainate application induced large Ca2+ transients in Bergmann glia cells. Second, in ion substitution experiments, when Ca2+ is the only extracellular permeant cation, the reversal potential corresponds to that expected for AMPA-R channels with a low permeability for Ca2+. Third, using a fluorometric flux-measurement approach (Schneggenburger et al., 1993a), we found that the Ca2+ fraction of the total cation current through AMPA-R channels is approximately 0.6%. This value is approximately sixfold lower than that found for recombinant AMPA-R lacking the AMPA-R subunit GluR2. Furthermore, single-cell RT-PCR experiments revealed the presence of the AMPA-R subunits GluR1, GluR2, and GluR3 in Purkinje neurons in cerebellar slices at developmental stages corresponding to those studied electrophysiologically. The expression of GluR2 in all cells tested (n = 14) is consistent with the subunit composition predicted from studies of recombinant AMPA-R channels with a low permeability for Ca2+ (Burnashev et al., 1992b). In conclusion, this study establishes that cerebellar Purkinje neurons at all postnatal developmental stages possess AMPA-R channels with a low permeability for Ca2+.
运用全细胞膜片钳记录、Fura-2荧光测定法以及单细胞逆转录(RT)-PCR相结合的方法,研究了大鼠小脑切片浦肯野神经元中AMPA受体(AMPA-R)通道的Ca(2+)通透特性。多条证据表明,在出生后发育的早期和晚期,浦肯野神经元均仅表达Ca2+通透性低的AMPA-R通道。首先,在用Ca2+指示剂Fura-2 AM加载的浦肯野神经元中,施加AMPA或海人酸时均未检测到Ca2+信号。相比之下,施加海人酸可在伯格曼胶质细胞中诱导出大的Ca2+瞬变。其次,在离子置换实验中,当Ca2+是唯一的细胞外渗透阳离子时,反转电位与Ca2+通透性低的AMPA-R通道预期的电位相对应。第三,使用荧光通量测量方法(施内根伯格等人,1993a),我们发现通过AMPA-R通道的总阳离子电流中的Ca2+部分约为0.6%。该值比缺乏AMPA-R亚基GluR2的重组AMPA-R的值低约六倍。此外,单细胞RT-PCR实验揭示了在与电生理研究阶段相对应的发育阶段,小脑切片中的浦肯野神经元中存在AMPA-R亚基GluR1、GluR2和GluR3。在所有测试细胞(n = 14)中GluR2的表达与对Ca2+通透性低的重组AMPA-R通道研究预测的亚基组成一致(布尔纳舍夫等人,1992b)。总之,本研究证实,出生后所有发育阶段的小脑浦肯野神经元均具有Ca2+通透性低的AMPA-R通道。