Literature DB >> 3053884

Epithelial restitution in the gastrointestinal tract.

E R Lacy1.   

Abstract

Injury to the gastrointestinal mucosa can be divided into two types: (a) deep injury involving extensive hemorrhage and large areas of tissue necrosis, and (b) superficial injury confined to the upper regions of the mucosa and not involving hemorrhagic lesions. Mucosal repair differs according to the severity of the damage. Repair of deep injury takes weeks because large regions of the mucosa must be replaced with new tissue, a process involving mitosis. Superficial injury is initially repaired rapidly over hours by epithelial restitution that does not involve mitosis but proceeds in the following sequence of events: First, the damaged surface epithelial cells are shed and form a layer that protects the restituting mucosa. Then the viable epithelial cells that remain attached to the mucosa at the margin of the wound become flattened and rapidly migrate over the denuded basal lamina. The superficial epithelium is re-established when migrating cells touch, form new tight junctions, and repolarize their organelles. This rapid protective mechanism, called restitution, has recently been documented in the stomach, duodenum, colon, and rectum. The cellular mechanisms, speed of migration, recovery of transmucosal electrical potential difference, and specific peculiarities of rapid epithelial restitution in the various regions of the gastrointestinal tract are reviewed here.

Entities:  

Mesh:

Year:  1988        PMID: 3053884     DOI: 10.1097/00004836-198812001-00012

Source DB:  PubMed          Journal:  J Clin Gastroenterol        ISSN: 0192-0790            Impact factor:   3.062


  32 in total

1.  Intestinal restitution: progression of actin cytoskeleton rearrangements and integrin function in a model of epithelial wound healing.

Authors:  M M Lotz; I Rabinovitz; A M Mercurio
Journal:  Am J Pathol       Date:  2000-03       Impact factor: 4.307

Review 2.  A guide to Ussing chamber studies of mouse intestine.

Authors:  Lane L Clarke
Journal:  Am J Physiol Gastrointest Liver Physiol       Date:  2009-04-02       Impact factor: 4.052

3.  Chemokine stimulation promotes enterocyte migration through laminin-specific integrins.

Authors:  Kimberle A Agle; Rebecca A Vongsa; Michael B Dwinell
Journal:  Am J Physiol Gastrointest Liver Physiol       Date:  2011-09-15       Impact factor: 4.052

Review 4.  Healing the epithelium: solving the problem from two sides.

Authors:  D K Podolsky
Journal:  J Gastroenterol       Date:  1997-02       Impact factor: 7.527

Review 5.  Amniotic fluid: Source of trophic factors for the developing intestine.

Authors:  Soham Dasgupta; Shreyas Arya; Sanjeev Choudhary; Sunil K Jain
Journal:  World J Gastrointest Pathophysiol       Date:  2016-02-15

6.  Rat small intestinal goblet cell kinetics in the process of restitution of surface epithelium subjected to ischemia-reperfusion injury.

Authors:  Hiroshi Ikeda; Chao-Long Yang; Jie Tong; Haruaki Nishimaki; Kenji Masuda; Tomohiro Takeo; Kenji Kasai; Gen Itoh
Journal:  Dig Dis Sci       Date:  2002-03       Impact factor: 3.199

7.  Prostaglandin E2 promotes intestinal repair through an adaptive cellular response of the epithelium.

Authors:  Hiroyuki Miyoshi; Kelli L VanDussen; Nicole P Malvin; Stacy H Ryu; Yi Wang; Naomi M Sonnek; Chin-Wen Lai; Thaddeus S Stappenbeck
Journal:  EMBO J       Date:  2016-10-24       Impact factor: 11.598

8.  Transforming growth factor-alpha (TGF-alpha) levels in human proximal gastrointestinal epithelium. Effect of mucosal injury and acid inhibition.

Authors:  J M Scheiman; K S Meise; J K Greenson; R J Coffey
Journal:  Dig Dis Sci       Date:  1997-02       Impact factor: 3.199

9.  In vivo action of trefoil factor 2 (TFF2) to speed gastric repair is independent of cyclooxygenase.

Authors:  Lin Xue; Eitaro Aihara; Daniel K Podolsky; Timothy C Wang; Marshall H Montrose
Journal:  Gut       Date:  2010-06-29       Impact factor: 23.059

10.  Junctional adhesion molecule A interacts with Afadin and PDZ-GEF2 to activate Rap1A, regulate beta1 integrin levels, and enhance cell migration.

Authors:  Eric A Severson; Winston Y Lee; Christopher T Capaldo; Asma Nusrat; Charles A Parkos
Journal:  Mol Biol Cell       Date:  2009-01-28       Impact factor: 4.138

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