Ordög Tamás, Baldo Marjolaine, Danko Reka, Sanders Kenton M
Department of Physiology and Cell Biology, University of Nevada, Reno School of Medicine, 89557, USA.
Gastroenterology. 2002 Dec;123(6):2028-40. doi: 10.1053/gast.2002.37056.
BACKGROUND & AIMS: Interstitial cells of Cajal (ICC) generate and propagate slow waves in the stomach. Gastric peristalsis depends on a proximal-to-distal gradient in slow wave frequency. We tested whether the gastric frequency gradient was an intrinsic property of ICC and whether dysrhythmias result from disruptions of ICC networks.
We studied wild-type (WT) and W/W(V) mice, which have only myenteric (pacemaker) ICC in the stomach. ICC distributions were analyzed by Kit immunofluorescence. Pacemaking in tissues was studied by intracellular electrophysiologic recording and in cultured ICC by monitoring mitochondrial [Ca(2+)] oscillations with rhod-2 fluorescence or membrane potential with DiBAC(4)(3) fluorescence.
Slow wave frequencies were constant throughout WT gastric muscle sheets containing corpus and antrum. Separating the antrum from the corpus caused a significant drop in antral slow wave frequency. ICC from WT antrums also displayed significantly slower pacemaker frequencies than corpus ICC, but the corpus pacemaker frequency dominated in cocultures of corpus and antrum ICC. Myenteric ICC networks were reduced in W/W(V) mice, particularly in the corpus. In W/W(V) mice, separating the antrum from the corpus failed to reduce antral slow wave frequency. Antral pacemaker frequency in ICC from W/W(V) stomachs was the same as in corpus ICC.
The proximal-to-distal slow wave frequency gradient and entrainment of distal electrical activity by proximal pacemakers are fundamental properties of gastric ICC. Chronic depletion of ICC networks disrupts the proximal-to-distal frequency gradient, and emergence of ectopic pacemakers in the antrum may be caused by "reprogramming" of the ICC pacemaker apparatus.
Cajal间质细胞(ICC)在胃中产生并传播慢波。胃蠕动依赖于慢波频率从近端到远端的梯度变化。我们测试了胃频率梯度是否为ICC的固有特性,以及心律失常是否由ICC网络破坏所致。
我们研究了野生型(WT)和W/W(V)小鼠,后者胃中仅存在肌间(起搏)ICC。通过Kit免疫荧光分析ICC分布。通过细胞内电生理记录研究组织中的起搏活动,在培养的ICC中通过用罗丹明-2荧光监测线粒体[Ca(2+)]振荡或用DiBAC(4)(3)荧光监测膜电位来研究起搏活动。
在包含胃体和胃窦的整个WT胃肌片中,慢波频率是恒定的。将胃窦与胃体分离导致胃窦慢波频率显著下降。来自WT胃窦的ICC的起搏频率也明显低于胃体ICC,但在胃体和胃窦ICC的共培养中,胃体起搏频率占主导。W/W(V)小鼠的肌间ICC网络减少,尤其是在胃体中。在W/W(V)小鼠中,将胃窦与胃体分离未能降低胃窦慢波频率。来自W/W(V)胃的ICC中的胃窦起搏频率与胃体ICC中的相同。
从近端到远端的慢波频率梯度以及近端起搏器对远端电活动的同步化是胃ICC的基本特性。ICC网络的慢性耗竭会破坏从近端到远端的频率梯度,胃窦中异位起搏器的出现可能是由ICC起搏装置的“重新编程”引起的。