Richards Kathryn S, Bommert Kurt, Szabo Gabor, Miles Richard
INSERM U739, CHU Pitié-Salpêtrière, 105 boulevard de l'Hôpital, 75013 Paris, France.
J Physiol. 2007 Dec 1;585(Pt 2):491-505. doi: 10.1113/jphysiol.2007.144733. Epub 2007 Oct 18.
The sodium pump (Na+/K+-ATPase), maintains intracellular and extracellular concentrations of sodium and potassium by catalysing ATP. Three sodium pump alpha subunits, ATP1A1, ATP1A2 and ATP1A3, are expressed in brain. We compared their role in pyramidal cells and a subset of interneurones in the subiculum. Interneurones were identified by their expression of GFP under the GAD-65 promoter. We used the sensitivity to the cardiac glycoside, ouabain, to discriminate between different alpha subunit isoforms. GFP-positive interneurones were depolarized by nanomolar doses of ouabain, but higher concentrations were needed to depolarize pyramidal cells. Comparison of pump currents in these cells revealed a current sensitive to low doses of ouabain in interneurones, while micromolar doses of ouabain were needed to suppress the pump current in subicular pyramidal cells. As predicted, nanomolar doses of ouabain increased the frequency but not the amplitudes of IPSPs in pyramidal cells. Immunostaining confirmed a differential distribution of alpha-subunits of the Na+/K+-ATPase in subicular interneurones and pyramidal cells. In conclusion, these data suggest that while ATP1A3-isoforms regulate sodium and potassium homeostasis in subicular interneurones, ATP1A1-isoforms assume this function in pyramidal cells. This differential expression of sodium pump isoforms may contribute to differences in resting membrane potential of subicular interneurones and pyramidal cells.
钠泵(Na⁺/K⁺-ATP酶)通过催化ATP来维持细胞内和细胞外钠和钾的浓度。钠泵的三个α亚基,即ATP1A1、ATP1A2和ATP1A3,在大脑中表达。我们比较了它们在海马下托锥体细胞和一部分中间神经元中的作用。通过在GAD-65启动子控制下绿色荧光蛋白(GFP)的表达来识别中间神经元。我们利用对强心苷哇巴因的敏感性来区分不同的α亚基异构体。纳摩尔剂量的哇巴因可使绿色荧光蛋白阳性的中间神经元去极化,但需要更高的浓度才能使锥体细胞去极化。对这些细胞中泵电流的比较显示,中间神经元中存在对低剂量哇巴因敏感的电流,而在海马下托锥体细胞中则需要微摩尔剂量的哇巴因来抑制泵电流。正如预期的那样,纳摩尔剂量的哇巴因增加了锥体细胞中抑制性突触后电位(IPSP)的频率,但没有增加其幅度。免疫染色证实了钠泵α亚基在海马下托中间神经元和锥体细胞中的分布差异。总之,这些数据表明,虽然ATP1A3异构体调节海马下托中间神经元中的钠和钾稳态,但ATP1A1异构体在锥体细胞中承担这一功能。钠泵异构体的这种差异表达可能导致海马下托中间神经元和锥体细胞静息膜电位的差异。