Furness John B, Robbins Heather L, Selmer Inger-Sofie, Hunne Billie, Chen Mao Xiang, Hicks Gareth A, Moore Stephen, Neylon Craig B
Department of Anatomy & Cell Biology and Centre for Neuroscience, University of Melbourne, 3010 Parkville, Victoria, Australia.
Cell Tissue Res. 2003 Nov;314(2):179-89. doi: 10.1007/s00441-003-0808-z. Epub 2003 Sep 26.
Recent functional evidence suggests that intermediate conductance calcium-activated potassium channels (IK channels) occur in neurons in the small intestine and in mucosal epithelial cells in the colon. This study was undertaken to investigate whether IK channel immunoreactivity occurs at these and at other sites in the gastrointestinal tract of the rat. IK channel immunoreactivity was found in nerve cell bodies throughout the gastrointestinal tract, from the esophagus to the rectum. It was revealed in the initial segments of the axons, but not in axon terminals. The majority of immunoreactive neurons had Dogiel type II morphology and in the myenteric plexus of the ileum all immunoreactive neurons were of this shape. Intrinsic primary afferent neurons in the rat small intestine are Dogiel type II neurons that are immunoreactive for calretinin, and it was found that almost all the IK channel immunoreactive neurons were also calretinin immunoreactive. IK channel immunoreactivity also occurred in calretinin-immunoreactive, Dogiel type II neurons in the caecum. Epithelial cells of the mucosal lining were immunoreactive in the esophagus, stomach, small and large intestines. In the intestines, the immunoreactivity occurred in transporting enterocytes, but not in mucous cells. Immunoreactivity was at both the apical and basolateral surfaces. A small proportion of mucosal endocrine cells was immunoreactive in the duodenum, ileum and caecum, but not in the stomach, proximal colon, distal colon or rectum. There was immunoreactivity of vascular endothelial cells. It is concluded that IK channels are located on cell bodies and proximal parts of axons of intrinsic primary afferent neurons, where, from functional studies, they would be predicted to lower neuronal excitability when opened in response to calcium entry. In the mucosa of the small and large intestine, IK channels are probably involved in control of potassium exchange, and in the esophageal and gastric mucosa they are possibly involved in control of cell volume in response to osmotic challenge.
近期的功能学证据表明,中电导钙激活钾通道(IK通道)存在于小肠神经元及结肠黏膜上皮细胞中。本研究旨在探究大鼠胃肠道的这些部位及其他部位是否存在IK通道免疫反应性。在从食管到直肠的整个胃肠道的神经细胞体中均发现了IK通道免疫反应性。在轴突的起始段有显示,但在轴突终末未发现。大多数免疫反应性神经元具有多极II型形态,在回肠的肌间神经丛中,所有免疫反应性神经元均为此种形态。大鼠小肠中的内源性初级传入神经元是对钙视网膜蛋白呈免疫反应性的多极II型神经元,并且发现几乎所有IK通道免疫反应性神经元也对钙视网膜蛋白呈免疫反应性。IK通道免疫反应性也出现在盲肠中对钙视网膜蛋白呈免疫反应性的多极II型神经元中。食管、胃、小肠和大肠的黏膜内衬上皮细胞呈免疫反应性。在肠道中,免疫反应性出现在转运肠上皮细胞中,而在黏液细胞中未出现。免疫反应性位于顶端和基底外侧表面。十二指肠、回肠和盲肠中有一小部分黏膜内分泌细胞呈免疫反应性,但胃、近端结肠、远端结肠或直肠中未出现。血管内皮细胞有免疫反应性。得出的结论是,IK通道位于内源性初级传入神经元的细胞体和轴突近端,从功能研究推测,当它们因钙内流而开放时会降低神经元兴奋性。在小肠和大肠黏膜中,IK通道可能参与钾交换的调控,而在食管和胃黏膜中,它们可能参与应对渗透压挑战时的细胞容积调控。