Role of myosin light chain kinase in intestinal epithelial barrier defects in a rat model of bowel obstruction
Open Access
- 20 April 2010
- journal article
- research article
- Published by Springer Nature in BMC Gastroenterology
- Vol. 10 (1) , 39
Abstract
Background: Bowel obstruction is a common cause of abdominal emergency, since the patients are at increased risk of septicemia resulting in high mortality rate. While the compartmentalized changes in enteric microfloral population and augmentation of bacterial translocation (BT) have already been reported using experimental obstruction models, alterations in epithelial permeability of the obstructed guts has not been studied in detail. Myosin light chain kinase (MLCK) is actively involved in the contraction of epithelial perijunctional actinomyosin ring and thereby increases paracellular permeability. In the current study we attempt to investigate the role of MLCK in epithelial barrier defects using a rat model of simple mechanical obstruction. Methods: Wistar rats received intraperitoneal injection of ML-7 (a MLCK inhibitor) or vehicle at 24, 12 and 1 hrs before and 12 hrs after intestinal obstruction (IO). The distal small intestine was obstructed with a single ligature placed 10 cm proximal to the ileocecal junction in IO rats for 24 hrs. Sham-operated rats served as controls. Results: Mucosal injury, such as villous blunting and increased crypt/villus ratio, was observed in the distal small intestine of IO rats. Despite massive enterocyte shedding, intestinal villi were covered with a contiguous epithelial layer without cell apoptosis. Increased transmural macromolecular flux was noticed in the distal small intestine and the proximal colon after IO. The bacterial colony forming units in the spleen and liver of IO rats were significantly higher than those of sham controls. Addition of ML-7 ameliorated the IO-triggered epithelial MLC phosphorylation, mucosal injury and macromolecular flux, but not the level of BT. Conclusions: The results suggest that IO-induced premature enterocytic sloughing and enhanced paracellular antigenic flux were mediated by epithelial MLCK activation. In addition, enteric bacteria may undergo transcytotic routes other than paracellular paths to cross the epithelium.Keywords
This publication has 47 references indexed in Scilit:
- Magnetic Resonance Imaging Detects Intestinal Barrier Dysfunction in a Rat Model of Acute Mesenteric Ischemia/Reperfusion InjuryInvestigative Radiology, 2009
- SGLT-1-mediated glucose uptake protects human intestinal epithelial cells against Giardia duodenalis-induced apoptosisInternational Journal for Parasitology, 2008
- INTESTINAL CROSSTALKShock, 2007
- Mechanism of IFN-γ-induced Endocytosis of Tight Junction Proteins: Myosin II-dependent Vacuolarization of the Apical Plasma MembraneMolecular Biology of the Cell, 2005
- Apoptosis inhibition plays a greater role than necrosis inhibition in decreasing bacterial translocation in experimental intestinal transplantation2005
- Regulation of MDCK cell-substratum adhesion by RhoA and myosin light chain kinase after ATP depletionAmerican Journal of Physiology-Cell Physiology, 2004
- Disruption of the Small-Intestine Mucosal Barrier After Intestinal Occlusion: A Study with Light and Electron MicroscopyJournal of Investigative Surgery, 2003
- An epithelial cell destined for apoptosis signals its neighbors to extrude it by an actin- and myosin-dependent mechanismCurrent Biology, 2001
- Outcome of Palliative Operations for Malignant Bowel Obstruction in Patients With Peritoneal Carcinomatosis From Nongynecological CancerAnnals of Surgical Oncology, 2001
- Maintenance of the macromolecular barrier at cell extrusion sites in intestinal epithelium: Physiological rearrangement of tight junctionsThe Journal of Membrane Biology, 1990