首页> 美国卫生研究院文献>The Journal of Physiology >Development of electrical rhythmicity in the murine gastrointestinal tract is specifically encoded in the tunica muscularis.
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Development of electrical rhythmicity in the murine gastrointestinal tract is specifically encoded in the tunica muscularis.

机译:鼠胃肠道中的电节律性的发展在肌膜中特别编码。

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摘要

1. Interstitial cells of Cajal (ICCs) have been identified as pacemaker cells in the gastrointestinal (GI) tracts of vertebrates. We have studied the development of ICCs in pacemaker regions and the onset of electrical rhythmicity in the gastric antrum, small bowel and proximal colon of the mouse. 2. ICCs, as detected by c-Kit immunofluorescence, were found during embryogenesis in regions of the GI tract that eventually become pacemaker areas. Prior to birth, these cells were organized into well-structured networks, and by the end of the embryonic period the morphology of ICC networks in pacemaker regions appeared very similar to that observed in adult animals. 3. Electrical rhythmicity was recorded prior to birth (by E18) in the proximal GI tract (stomach and jejunum), and this activity developed to adult-like behaviour within a week after birth. In the ileum and proximal colon rhythmicity developed after birth, and adult-like characteristics were apparent within the first week. 4. Post-junctional responses of smooth muscles to neural inputs could be recorded at birth, and stimulation of intrinsic nerves often led to oscillatory activity resembling slow waves for up to several minutes following brief stimuli. Nerve stimulation augmented spontaneous activity in the proximal portions of the GI tract and elicited rhythmic activity temporarily in quiescent tissues of the distal GI tract. 5. ICCs and rhythmicity developed in an apparently normal manner in tissues isolated at birth and placed in organ culture. These data suggest that the tunica muscularis provides a suitable microenvironment for the development of ICCs and rhythmicity without the need for extrinsic stimuli. 6. Treatment of small intestinal tissues taken from embryos at E15 with neutralizing c-Kit antibodies abolished ICC development and the organization of ICCs into networks that typically occurs during the late embryonic period. Treatment of muscles taken from newborn animals with c-Kit antibodies blocked postnatal development of ICCs, disrupted already established and functional ICC networks, and rendered muscles electrically quiescent. 7. In summary, ICC networks develop in the pacemaker regions of the murine GI tract before birth. Development and organization of ICCs of the myenteric plexus region into networks precedes the development of electrical rhythmicity. Post-natal development of electrical rhythmicity is mainly characterized by enhancement of the amplitude and frequency of slow waves. The development of ICCs and electrical rhythmicity persists in vitro. ICCs appear to be necessary for the initiation of electrical rhythmicity. These findings provide further evidence for the pacemaker role of ICCs.
机译:1. Cajal间质细胞(ICC)已被确定为脊椎动物胃肠道(GI)中的起搏器细胞。我们已经研究了心脏起搏器区域ICC的发展以及小鼠胃窦,小肠和近端结肠的节律性发作。 2.通过c-Kit免疫荧光检测到的ICC在胚胎发生期间的胃肠道区域被发现,该区域最终成为起搏器区域。在出生之前,这些细胞被组织成结构良好的网络,到胚胎期末,起搏器区域的ICC网络的形态看起来与成年动物非常相似。 3.在出生前(通过E18)在近端的胃肠道(胃和空肠)中记录了电节律,这种活动在出生后一周内发展为成年人的行为。出生后回肠和近端结肠有节律,在第一周内明显出现成人样特征。 4.出生时可记录平滑肌对神经输入的连接后反应,对内在神经的刺激通常会导致短暂的刺激后长达数分钟的类似于慢波的振荡活动。神经刺激增强了胃肠道近端的自发活动,并在远端胃肠道的静止组织中暂时引起了节律性活动。 5.在出生时分离并置于器官培养物中的组织中,ICC和节律性以明显正常的方式发展。这些数据表明,肌外膜为ICC的发展和节律性提供了合适的微环境,而无需外部刺激。 6.用中和性c-Kit抗体处理在E15取自胚胎的小肠组织,从而消除了ICC的发育,并消除了ICC进入通常在胚胎后期发生的网络的组织。用c-Kit抗体处理新生动物的肌肉,会阻止ICC的出生后发展,破坏已经建立的功能性ICC网络,并使肌肉呈静态。 7.总之,ICC网络在出生前在小鼠胃肠道的起搏器区域发展。肌丛神经区域的ICC的发展和组织成网络先于电节律的发展。产后电节律的发展主要特征是慢波的振幅和频率增加。 ICC和电节律性的发展在体外持续存在。 ICC似乎是开始电节律所必需的。这些发现为ICC的起搏器作用提供了进一步的证据。

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