Department of Physiology & Cell Biology, University of Nevada, Reno School of Medicine, Reno, NV, 89557, USA.
Sci Rep. 2019 Mar 13;9(1):4402. doi: 10.1038/s41598-019-39729-7.
Spontaneous excitability and contractions of colonic smooth muscle cells (SMCs) are normally suppressed by inputs from inhibitory motor neurons, a behavior known as tonic inhibition. The post-junctional cell(s) mediating tonic inhibition have not been elucidated. We investigated the post-junctional cells mediating tonic inhibition in the proximal colon and whether tonic inhibition results from suppression of the activity of Ano1 channels, which are expressed exclusively in interstitial cells of Cajal (ICC). We found that tetrodotoxin (TTX), an inhibitor of nitric oxide (NO) synthesis, L-NNA, and an inhibitor of soluble guanylyl cyclase, ODQ, greatly enhanced colonic contractions. Ano1 antagonists, benzbromarone and Ani9 inhibited the effects of TTX, L-NNA and ODQ. Ano1 channels are activated by Ca release from the endoplasmic reticulum (ER) in ICC, and blocking Ca release with a SERCA inhibitor (thapsigargin) or a store-operated Ca entry blocker (GSK 7975 A) reversed the effects of TTX, L-NNA and ODQ. Ca imaging revealed that TTX, L-NNA and ODQ increased Ca transient firing in colonic ICC. Our results suggest that tonic inhibition in the proximal colon occurs through suppression of Ca release events in ICC. Suppression of Ca release in ICC limits the open probability of Ano1 channels, reducing the excitability of electrically-coupled SMCs.
肠平滑肌细胞(SMC)的自发性兴奋和收缩通常受到抑制性运动神经元输入的抑制,这种行为称为紧张性抑制。介导紧张性抑制的突触后细胞尚未阐明。我们研究了近端结肠中介导紧张性抑制的突触后细胞,以及紧张性抑制是否源于抑制表达于平滑肌细胞缝隙连接的 Ano1 通道的活性。我们发现,河豚毒素(TTX),一氧化氮(NO)合成的抑制剂,L-NNA,和可溶性鸟苷酸环化酶的抑制剂,ODQ,极大地增强了结肠收缩。Ano1 拮抗剂苯溴马隆和 Ani9 抑制了 TTX、L-NNA 和 ODQ 的作用。Ano1 通道在 ICC 中由内质网(ER)释放 Ca 激活,用 SERCA 抑制剂(毒胡萝卜素)或储存操作 Ca 进入阻滞剂(GSK 7975A)阻断 Ca 释放可逆转 TTX、L-NNA 和 ODQ 的作用。钙成像显示 TTX、L-NNA 和 ODQ 增加了结肠 ICC 中的钙瞬变发射。我们的结果表明,近端结肠的紧张性抑制是通过抑制 ICC 中的 Ca 释放事件发生的。ICC 中 Ca 释放的抑制限制了 Ano1 通道的开放概率,降低了电耦联 SMC 的兴奋性。