4.6 Article

Sonic Hedgehog contributes to gastric mucosal restitution after injury

期刊

LABORATORY INVESTIGATION
卷 93, 期 1, 页码 96-111

出版社

NATURE PUBLISHING GROUP
DOI: 10.1038/labinvest.2012.148

关键词

gastric ulcer; Helicobacter pylori (H. pylori); macrophages; re-epithelialization; tissue repair

资金

  1. NIH [1R01DK083402, RO1 DK071590, AR-47363]
  2. Digestive Health Center Cincinnati Children's Medical Health Center (DHC) [CHTF/SUB DK078392]
  3. Department of Veterans Affairs
  4. AGA Funderburg Award in Gastric Biology Related to Cancer
  5. Vanderbilt Digestive Disease Research Center [P30 DK58404]
  6. Vanderbilt-Ingram Cancer Center [CA68485]
  7. NATIONAL CANCER INSTITUTE [P30CA068485] Funding Source: NIH RePORTER
  8. NATIONAL INSTITUTE OF ARTHRITIS AND MUSCULOSKELETAL AND SKIN DISEASES [P30AR047363] Funding Source: NIH RePORTER
  9. NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES [R01DK083402, P30DK058404, R01DK071590, T35DK060444, P30DK078392] Funding Source: NIH RePORTER

向作者/读者索取更多资源

Eradication of Helicobacter pylori correlates with regeneration of the gastric epithelium, ulcer healing and re-expression of the gastric morphogen Sonic Hedgehog (Shh). We sought to identify the role of Shh as a regulator of gastric epithelial regeneration during wound healing. A mouse model expressing a parietal cell-specific, tamoxifen-inducible deletion of Shh (HKCre(ERT2); Shh(flox/flox) or PC-iShhKO) was developed. Stomachs were collected and compared 7-150 days after the final vehicle or tamoxifen injection. Ulcers were induced in both controls and PC-iShhKO mice using acetic acid and ulcer size compared 1 and 7 days post induction. (1) Re-expression of Shh correlates with decreased hyperproliferation: Compared to controls, PC-iShhKO mice developed foveolar hyperplasia. Restoration of normal gastric epithelial architecture and differentiation correlated with the re-expression of Shh in PC-iShhKO mice 150 days after the final tamoxifen injection. At the tamoxifen dose used to induce Cre recombination there was no genotoxicity reported in either HKCre(ERT2) or Shh(flox/flox) control mouse stomachs. (2) Delayed wound healing in PC-iShhKO mouse stomachs: To identify the role of Shh in gastric regeneration, an acetic acid ulcer was induced in control and PC-iShhKO mice. Ulcers began to heal in control mice by 7 days after induction. Ulcer healing was documented by decreased ulcer size, angiogenesis, macrophage infiltration and formation of granulation tissue that correlated with the re-expression of Shh within the ulcerated tissue. PC-iShhKO mice did not show evidence of ulcer healing. Re-expression of Shh contributes to gastric regeneration. Our current study may have clinical implications given that eradication of H. pylori correlates with re-expression of Shh, regeneration of the gastric epithelium and ulcer healing. Laboratory Investigation (2013) 93, 96-111; doi:10.1038/labinvest.2012.148; published online 22 October 2012

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