Lu Ping, Chen Jun, Zhang Chenghai, Saur Dieter, Baer Christina E, Lifshitz Lawrence M, Fogarty Kevin E, ZhuGe Ronghua
Department of Microbiology and Physiological Systems, University of Massachusetts Medical School, Worcester, Massachusetts, USA.
Division of Pulmonary Diseases, State Key Laboratory of Biotherapy, and Department of Respiratory and Critical Care Medicine, West China Hospital of Sichuan University, Chengdu, China.
J Cell Physiol. 2021 Aug;236(8):5937-5952. doi: 10.1002/jcp.30279. Epub 2021 Jan 16.
A persistent basal tone in the internal anal sphincter (IAS) is essential for keeping the anal canal closed and fecal continence; its inhibition via the rectoanal inhibitory reflex (RAIR) is required for successful defecation. However, cellular signals underlying the IAS basal tone remain enigmatic. Here we report the origin and molecular mechanisms of calcium signals that control the IAS basal tone, using a combination approach including a novel IAS slice preparation that retains cell arrangement and architecture as in vivo, 2-photon imaging, and cell-specific gene-modified mice. We found that IAS smooth muscle cells generate two forms of contractions (i.e., phasic and sustained contraction) and Ca signals (i.e., synchronized Ca oscillations [SCaOs] and asynchronized Ca oscillations [ACaOs]) that last for hours. RyRs, TMEM16A, L-type Ca channels, and gap junctions are required for SCaOs, which account for phasic contraction and 75% of sustained contraction. Nevertheless, only RyRs are required for ACaOs, which contribute 25% of sustained contraction. Nitric oxide, the primary neurotransmitter mediating the RAIR, blocks both types of Ca signals, leading to IAS's full relaxation. Our results show that the oscillating nature of Ca signals generates and maintains the basal tone without causing cytotoxicity to IAS. Our study provides insight into fecal continence and normal defecation.
肛门内括约肌(IAS)持续的基础张力对于保持肛管闭合和排便节制至关重要;通过直肠肛管抑制反射(RAIR)对其进行抑制是成功排便所必需的。然而,IAS基础张力背后的细胞信号仍然是个谜。在这里,我们使用包括一种新型IAS切片制备(其保留了体内的细胞排列和结构)、双光子成像和细胞特异性基因修饰小鼠在内的组合方法,报告了控制IAS基础张力的钙信号的起源和分子机制。我们发现,IAS平滑肌细胞产生两种形式的收缩(即相位性收缩和持续性收缩)以及持续数小时的钙信号(即同步钙振荡[SCaOs]和异步钙振荡[ACaOs])。SCaOs需要兰尼碱受体(RyRs)、跨膜蛋白16A(TMEM16A)、L型钙通道和缝隙连接,它们负责相位性收缩以及75%的持续性收缩。然而,ACaOs仅需要RyRs,它们贡献了25%的持续性收缩。一氧化氮是介导RAIR的主要神经递质,它阻断这两种类型的钙信号,导致IAS完全松弛。我们的结果表明,钙信号的振荡性质产生并维持基础张力,而不会对IAS造成细胞毒性。我们的研究为排便节制和正常排便提供了见解。