Y. M. Usachev: Department of Pharmacology, University of Iowa Carver College of Medicine, 2-340F BSB, 51 Newton Road, Iowa City, IA 52242, USA.
J Physiol. 2013 May 15;591(10):2443-62. doi: 10.1113/jphysiol.2012.249219. Epub 2013 Feb 4.
The central processes of primary nociceptors form synaptic connections with the second-order nociceptive neurons located in the dorsal horn of the spinal cord. These synapses gate the flow of nociceptive information from the periphery to the CNS, and plasticity at these synapses contributes to centrally mediated hyperalgesia and allodynia. Although exocytosis and synaptic plasticity are controlled by Ca(2+) at the release sites, the mechanisms underlying presynaptic Ca(2+) signalling at the nociceptive synapses are not well characterized. We examined the presynaptic mechanisms regulating Ca(2+) clearance following electrical stimulation in capsaicin-sensitive nociceptors using a dorsal root ganglion (DRG)/spinal cord neuron co-culture system. Cytosolic Ca(2+) concentration ([Ca(2+)]i) recovery following electrical stimulation was well approximated by a monoexponential function with a ∼2 s. Inhibition of sarco-endoplasmic reticulum Ca(2+)-ATPase did not affect presynaptic [Ca(2+)]i recovery, and blocking plasmalemmal Na(+)/Ca(2+) exchange produced only a small reduction in the rate of [Ca(2+)]i recovery (∼12%) that was independent of intracellular K(+). However, [Ca(2+)]i recovery in presynaptic boutons strongly depended on the plasma membrane Ca(2+)-ATPase (PMCA) and mitochondria that accounted for ∼47 and 40%, respectively, of presynaptic Ca(2+) clearance. Measurements using a mitochondria-targeted Ca(2+) indicator, mtPericam, demonstrated that presynaptic mitochondria accumulated Ca(2+) in response to electrical stimulation. Quantitative analysis revealed that the mitochondrial Ca(2+) uptake is highly sensitive to presynaptic [Ca(2+)]i elevations, and occurs at [Ca(2+)]i levels as low as ∼200-300 nm. Using RT-PCR, we detected expression of several putative mitochondrial Ca(2+) transporters in DRG, such as MCU, Letm1 and NCLX. Collectively, this work identifies PMCA and mitochondria as the major regulators of presynaptic Ca(2+) signalling at the first sensory synapse, and underlines the high sensitivity of the mitochondrial Ca(2+) uniporter in neurons to cytosolic Ca(2+).
初级伤害感受器的中枢过程与位于脊髓背角的二阶伤害感受神经元形成突触连接。这些突触控制着来自外周的伤害信息流向中枢神经系统,而这些突触的可塑性有助于中枢介导的痛觉过敏和感觉异常。尽管外排和突触可塑性由释放部位的 Ca(2+)控制,但伤害性突触的突触前 Ca(2+)信号转导的机制尚未很好地描述。我们使用背根神经节 (DRG)/脊髓神经元共培养系统研究了电刺激后调节辣椒素敏感伤害感受器中 Ca(2+)清除的突触前机制。电刺激后细胞溶质 Ca(2+)浓度 ([Ca(2+)]i) 的恢复很好地用单指数函数来近似,半衰期约为 2 秒。肌浆网内质网 Ca(2+)-ATP 酶的抑制作用并不影响突触前 [Ca(2+)]i 的恢复,而阻断质膜 Na(+)/Ca(2+) 交换仅使 [Ca(2+)]i 恢复率降低约 12%(不依赖于细胞内 K(+))。然而,突触前末梢中 [Ca(2+)]i 的恢复强烈依赖于质膜 Ca(2+)-ATP 酶 (PMCA) 和线粒体,它们分别占突触前 Ca(2+)清除的约 47%和 40%。使用靶向线粒体的 Ca(2+)指示剂 mtPericam 的测量表明,突触前线粒体在电刺激下积累 Ca(2+)。定量分析表明,线粒体 Ca(2+)摄取对突触前 [Ca(2+)]i 升高非常敏感,并且发生在 [Ca(2+)]i 水平低至约 200-300nm。通过 RT-PCR,我们在 DRG 中检测到几种假定的线粒体 Ca(2+)转运体的表达,如 MCU、Letm1 和 NCLX。总的来说,这项工作确定了 PMCA 和线粒体是第一感觉突触突触前 Ca(2+)信号的主要调节因子,并强调了神经元中线粒体 Ca(2+)单向转运体对细胞溶质 Ca(2+)的高敏感性。