Persistent distention of colon damages interstitial cells of Cajal through Ca 2+ ‐ ERK ‐ AP ‐1‐ miR‐34c ‐ SCF deregulation

• Published in: Journal of cellular and molecular medicine Vol. 21; no. 9; pp. 1881 - 1892
• Main Authors: Yang, Shu, Dong, Fang, Li, Dandan, Sun, Haimei, Wu, Bo, Sun, Tingyi, Wang, Yaxi, Shen, Ping, Ji, Fengqing, Zhou, Deshan
• Format: Journal Article
• Language: English
• Published: England John Wiley & Sons, Inc 01.09.2017
• Subjects: Activator protein 1; Animals; c-Jun protein; Calcium - metabolism; Calcium signalling; Colon; Colon - pathology; Diabetes mellitus; Disease Models, Animal; Down-Regulation - genetics; Enzyme Activation; Extracellular signal-regulated kinase; Extracellular Signal-Regulated MAP Kinases - metabolism; Gastric motility; Hirschsprung's disease; Humans; Interstitial cells; Interstitial cells of Cajal; Interstitial Cells of Cajal - metabolism; Interstitial Cells of Cajal - pathology; Male; MAP Kinase Signaling System - genetics; Mice; Mice, Inbred BALB C; MicroRNAs - genetics; MicroRNAs - metabolism; miRNA; Models, Biological; Myocytes, Smooth Muscle - metabolism; Paresis; Polymerase chain reaction; Proto-Oncogene Proteins c-jun - metabolism; Rodents; Smooth muscle; Stem Cell Factor - genetics; Stem Cell Factor - metabolism; Transcription Factor AP-1 - metabolism; Transcription factors; Transcription, Genetic; interstitial cell of Cajal; stretch; stem cell factor; AP-1/c-Jun; gastrointestinal motility disorder; miR-34c; distention
• ISSN: 1582-1838; 1582-4934
• DOI: 10.1111/jcmm.13108

Gastrointestinal motility disorders ( GMD s) are attributed to loss of interstitial cells of Cajal ( ICC ), whose survival and function are deeply dependent on the activation of KIT / SCF signalling. Based on the facts that gastrointestinal distention is common in GMD patients and SCF produced by smooth muscle cells ( SMC s) is usually decreased before ICC loss, we considered a possible contribution of persistent gastrointestinal distention/stretch to SCF deficiency. In this study, chronic colonic distention mouse model, diabetic gastrointestinal paresis mouse model, cultured mouse colonic SMC s and colon specimens from Hirschsprung's disease patients were used. The results showed that SCF was clearly decreased in distent colon of mice and patients, and micro RNA array and real‐time PCR indicated a concomitant increase of miR‐34c in distent colon. A negative regulation of miR‐34c on SCF expression was confirmed by luciferase reporter assays together with knock‐down and overexpression of miR‐34c in cultured colonic SMC s. Using EMSA and Ch IP assays, we further consolidated that in response to persistent stretch, the transcription factor AP ‐1/c‐Jun was highly activated in colonic SMC s and significantly promoted miR‐34c transcription by binding to miR‐34c promoter. Knock‐down or overexpression of AP ‐1/c‐Jun in cultured colonic SMC s leads to down‐ or up‐regulation of miR‐34c , respectively. In addition, the activation of AP ‐1/c‐Jun was through ERK 1/2 signalling provoked by Ca 2+ overload in colonic SMC s that were subject to persistent stretch. In conclusion, our data demonstrated that persistent distention/stretch on colonic SMC s could suppress SCF production probably through Ca 2+ ‐ ERK ‐ AP ‐1‐ miR‐34c deregulation, resulting in ICC loss or impairment and GMD progress.