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Distribution of voltage-dependent and intracellular Ca2+ channels in submucosal neurons from rat distal colon

机译:大鼠远端结肠黏膜下神经元中电压依赖性和细胞内钙离子通道的分布

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We recently observed a bradykinin-induced increase in the cytosolic Ca 2+ concentration in submucosal neurons of rat colon, an increase inhibited by blockers of voltage-dependent Ca2+ (Cav) channels. As the types of Cav channels used by this part of the enteric nervous system are unknown, the expression of various Cav subunits has been investigated in whole-mount submucosal preparations by immunohistochemistry. Submucosal neurons, identified by a neuronal marker (microtubule-associated protein 2), are immunoreactive for Cav1.2, Cav1.3 and Cav2.2, expression being confirmed by reverse transcription plus the polymerase chain reaction. These data agree with previous observations that the inhibition of L- and N-type Ca2+ currents strongly inhibits the response to bradykinin. However, whole-cell patch-clamp experiments have revealed that bradykinin does not enhance Ca2+ inward currents under voltage-clamp conditions. Consequently, bradykinin does not directly interact with Cav channels. Instead, the kinin-induced Ca2+ influx is caused indirectly by the membrane depolarization evoked by this peptide. As intracellular Ca2+ channels on Ca 2+-storing organelles can also contribute to Ca2+ signaling, their expression has been investigated by imaging experiments and immunohistochemistry. Inositol 1,4,5-trisphosphate (IP3) receptors (IP3R) have been functionally demonstrated in submucosal neurons loaded with the Ca2+-sensitive fluorescent dye, fura-2. Histamine, a typical agonist coupled to the phospholipase C pathway, induces an increase in the fura-2 signal ratio, which is suppressed by 2-aminophenylborate, a blocker of IP3 receptors. The expression of IP3R1 has been confirmed by immunohistochemistry. In contrast, ryanodine, tested over a wide concentration range, evokes no increase in the cytosolic Ca2+ concentration nor is there immunohistochemical evidence for the expression of ryanodine receptors in these neurons. Thus, rat submucosal neurons are equipped with various types of high-voltage activated Cav channels and with IP3 receptors for intracellular Ca2+ signaling.
机译:我们最近观察到缓激肽诱导的大鼠结肠粘膜下神经元胞浆Ca 2+浓度增加,该增加受到电压依赖性Ca2 +(Cav)通道阻滞剂的抑制。由于肠神经系统的这一部分使用的Cav通道类型尚不清楚,因此已通过免疫组织化学研究了在整个黏膜下制剂中各种Cav亚基的表达。由神经元标记物(微管相关蛋白2)鉴定的粘膜下神经元对Cav1.2,Cav1.3和Cav2.2具有免疫反应性,其表达可通过逆转录和聚合酶链反应得到证实。这些数据与以前的观察结果一致,即抑制L型和N型Ca2 +电流强烈抑制了对缓激肽的反应。然而,全细胞膜片钳实验表明,缓激肽在电压钳制条件下不会增强Ca2 +内向电流。因此,缓激肽不会直接与Cav通道相互作用。相反,激肽诱导的Ca2 +流入是由该肽引起的膜去极化间接引起的。由于储存Ca 2+的细胞器上的细胞内Ca2 +通道也可以促进Ca2 +信号传导,因此已通过成像实验和免疫组织化学研究了它们的表达。肌醇1,4,5-三磷酸(IP3)受体(IP3R)已在功能强大的Ca2 +敏感荧光染料fura-2的粘膜下神经元中得到证实。组胺是一种典型的与磷脂酶C途径偶联的激动剂,可引起fura-2信号比率的增加,而2-氨基苯基硼酸盐(一种IP3受体的阻滞剂)可抑制呋喃2信号的比率。 IP3R1的表达已通过免疫组织化学证实。相反,在较宽的浓度范围内测试的莱丹碱不会引起胞浆Ca2 +浓度增加,也没有免疫组化证据表明莱丹碱受体在这些神经元中的表达。因此,大鼠粘膜下神经元配备有各种类型的高压激活的Cav通道和IP3受体,用于细胞内Ca2 +信号传导。

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