Strege Peter R, Gibbons Simon J, Mazzone Amelia, Bernard Cheryl E, Beyder Arthur, Farrugia Gianrico
Enteric NeuroScience Program, Mayo Clinic, Rochester, Minnesota.
Enteric NeuroScience Program, Mayo Clinic, Rochester, Minnesota
Am J Physiol Gastrointest Liver Physiol. 2017 Jun 1;312(6):G572-G579. doi: 10.1152/ajpgi.00429.2016. Epub 2017 Mar 23.
Anoctamin1 (Ano1 and TMEM16A) is a calcium-activated chloride channel specifically expressed in the interstitial cells of Cajal (ICC) of the gastrointestinal tract muscularis propria. Ano1 is necessary for normal electrical slow waves and ICC proliferation. The full-length human Ano1 sequence includes an additional exon, exon "0," at the NH terminus. Ano1 with exon 0 [Ano1] had a lower EC for intracellular calcium ([Ca]) and faster chloride current () kinetics. The Ano1 alternative splice variant with segment "c" encoding exon 13 expresses on the first intracellular loop four additional amino acid residues, EAVK, which alter at low [Ca] Exon 13 is expressed in 75-100% of Ano1 transcripts in most human tissues but only 25% in the human stomach. Our aim was to determine the effect of EAVK deletion on Ano1 parameters. By voltage-clamp electrophysiology, we examined in HEK293 cells transiently expressing Ano1 with or without the EAVK sequence [Ano1ΔEAVK]. The EC values of activating and deactivating for [Ca] were 438 ± 7 and 493 ± 9 nM for Ano1 but higher for Ano1ΔEAVK at 746 ± 47 and 761 ± 26 nM, respectively. Meanwhile, the EC values for the ratio of instantaneous to steady-state were not different between variants. Congruently, the time constant of activation was slower for Ano1ΔEAVK than Ano1 currents at intermediate [Ca] These results suggest that EAVK decreases the calcium sensitivity of Ano1 current activation and deactivation by slowing activation kinetics. Differential expression of EAVK in the human stomach may function as a switch to increase sensitivity to [Ca] via faster gating of Ano1. Calcium-activated chloride channel anoctamin1 (Ano1) is necessary for normal slow waves in the gastrointestinal interstitial cells of Cajal. Exon 0 encodes the NH terminus of full-length human Ano1 [Ano1], while exon 13 encodes residues EAVK on its first intracellular loop. Splice variants lack EAVK more often in the stomach than other tissues. Ano1 without EAVK [Ano1ΔEAVK] has reduced sensitivity for intracellular calcium, attributable to slower kinetics. Differential expression of EAVK may function as a calcium-sensitive switch in the human stomach.
anoctamin1(Ano1和TMEM16A)是一种钙激活氯离子通道,在胃肠道固有肌层的Cajal间质细胞(ICC)中特异性表达。Ano1对于正常的电慢波和ICC增殖是必需的。全长人Ano1序列在NH末端包含一个额外的外显子,即外显子“0”。带有外显子0的Ano1 [Ano1]对细胞内钙([Ca])的EC较低,且氯离子电流()动力学更快。带有编码外显子13的片段“c”的Ano1可变剪接变体在第一个细胞内环上表达另外四个氨基酸残基EAVK,这在低[Ca]时会改变。外显子13在大多数人体组织中75 - 100%的Ano1转录本中表达,但在人胃中仅为25%。我们的目的是确定EAVK缺失对Ano1参数的影响。通过电压钳电生理学,我们在瞬时表达带有或不带有EAVK序列的Ano1 [Ano1ΔEAVK]的HEK293细胞中检测了。对于[Ca],Ano1激活和失活 的EC值分别为438±7和493±9 nM,但Ano1ΔEAVK的更高,分别为746±47和761±26 nM。同时,变体之间瞬时与稳态 比值的EC值没有差异。同样,在中等[Ca]时,Ano1ΔEAVK的激活时间常数比Ano1电流慢。这些结果表明,EAVK通过减缓激活动力学降低了Ano1电流激活和失活的钙敏感性。EAVK在人胃中的差异表达可能通过Ano1更快的门控作用作为增加对[Ca]敏感性的开关。钙激活氯离子通道anoctamin1(Ano1)对于胃肠道Cajal间质细胞中的正常慢波是必需的。外显子0编码全长人Ano1 [Ano1]的NH末端,而外显子13在其第一个细胞内环上编码残基EAVK。剪接变体在胃中比其他组织更常缺少EAVK。没有EAVK的Ano1 [Ano1ΔEAVK]对细胞内钙的敏感性降低,这归因于较慢动力学。EAVK的差异表达可能在人胃中作为钙敏感开关起作用。