4.6 Article

Annexin 2 regulates intestinal epithelial cell spreading and wound closure through Rho-related signaling

Journal

AMERICAN JOURNAL OF PATHOLOGY
Volume 170, Issue 3, Pages 951-966

Publisher

ELSEVIER SCIENCE INC
DOI: 10.2353/ajpath.2007.060647

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Funding

  1. NHLBI NIH HHS [R01 HL072124, HL72124] Funding Source: Medline
  2. NIDDK NIH HHS [5T32DK07771, DK59888, R01 DK055679, F32 DK066930, T32 DK007771, U01 DK060379, DK72564, R24 DK064399, R01 DK072564, R29 DK055679, DK55679, R01 DK059888, 1F32DK066930-01, DK60379, DK64399] Funding Source: Medline
  3. NIGMS NIH HHS [T32 GM008169] Funding Source: Medline

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Epithelial cell migration is a critical event in gastrointestinal mucosal wound healing and is dependent on actin cytoskeletal reorganization. We observed increased expression of an actin regulatory protein, annexin 2, in migrating intestinal epithelial cells. Small interfering RNA (siRNA)-mediated knockdown of annexin 2 expression in Caco-2 epithelial cells resulted in significant reductions in cell spreading and wound closure associated with. decreased formation of filamentous actin bundles along the base of migrating cells. Because annexin 2 has been shown to influences actin cytoskeletal remodeling through targeting signaling molecules to membrane domains, we examined the membrane association and activation status of Rho GTPases after annexin 2 knockdown. We observed Rho dissociation from membranes and decreased Rho activity following annexin 2 siRNA transfection. Inhibition of cell spreading and wound closure in annexin 2 siRNA-transfected cells was prevented by expression of constitutively active RhoA. Rho colocallized with annexin 2 in lamellipodia and along the cytoplasmic face of the plasma membrane. in addition, annexin 2 was observed to co-immunoprecipitate with endogenous; Rho and constitutively active RhoA These findings suggest that annexin 2 plays a role in targeting Rho to cellular membranes, thereby modulating Rho-related signaling events regulating cytoskeletal reorganization during epithelial cell migration.

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