Localization and potential function of kindlin-1 in periodontal tissues

Eur J Oral Sci. 2009 Oct;117(5):518-27. doi: 10.1111/j.1600-0722.2009.00651.x.

Abstract

Kindlin-1 is an intracellular focal adhesion protein that regulates the actin cytoskeleton. Patients suffering from Kindler syndrome have a homologous mutation of the kindlin-1 gene and develop skin blisters, periodontal disease, and intestinal complications because of deficient adhesion of the basal epithelial cells. We investigated kindlin-1 localization in periodontal tissue and its functions in cultured keratinocytes and showed that kindlin-1 co-localizes with migfilin and paxillin in the basal epithelial cells of oral mucosa and in cultured keratinocytes. The kindlin-1-deficient oral mucosal tissue from a patient with Kindler syndrome showed a complete lack of paxillin and reduced migfilin immunostaining in the basal keratinocytes. Co-immunoprecipitation showed that migfilin directly interacted with kindlin-1. RNA interference-induced kindlin-1 deficiency in keratinocytes led to an altered distribution of migfilin-containing focal adhesions, reduced cell spreading, decreased cell proliferation, and decelerated cell migration. Disruption of microtubules in the kindlin-1-deficient cells further reduced cell spreading, suggesting that microtubules can partially compensate for kindlin-1 deficiency. Kindlin-1 supported mature cell-extracellular matrix adhesions of keratinocytes, as downregulation of kindlin-1 expression significantly reduced the cell-adhesion strength. In summary, kindlin-1 interacts with migfilin and plays a crucial role in actin-dependent keratinocyte cell adhesion essential for epidermal and periodontal health.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Cell Adhesion / physiology
  • Cell Adhesion Molecules / analysis
  • Cell Line, Tumor
  • Cell Movement / physiology
  • Cell Proliferation
  • Cytoskeletal Proteins / analysis
  • Epithelial Cells / pathology
  • Extracellular Matrix / ultrastructure
  • Focal Adhesions / ultrastructure
  • Humans
  • Intestinal Diseases / genetics
  • Keratinocytes / pathology
  • Membrane Proteins / analysis*
  • Membrane Proteins / genetics
  • Membrane Proteins / physiology
  • Microtubules / ultrastructure
  • Mouth Mucosa / pathology
  • Neoplasm Proteins / analysis*
  • Neoplasm Proteins / genetics
  • Neoplasm Proteins / physiology
  • Paxillin / analysis
  • Periodontal Diseases / genetics
  • Periodontium / pathology*
  • Protein Serine-Threonine Kinases / analysis
  • RNA Interference
  • Skin Diseases, Genetic / pathology
  • Skin Diseases, Vesiculobullous / genetics
  • Syndrome

Substances

  • Cell Adhesion Molecules
  • Cytoskeletal Proteins
  • FBLIM1 protein, human
  • FERMT1 protein, human
  • FERMT3 protein, human
  • Membrane Proteins
  • Neoplasm Proteins
  • Paxillin
  • integrin-linked kinase
  • Protein Serine-Threonine Kinases