1. Academic Validation
  2. Histatin-1, a histidine-rich peptide in human saliva, promotes cell-substrate and cell-cell adhesion

Histatin-1, a histidine-rich peptide in human saliva, promotes cell-substrate and cell-cell adhesion

  • FASEB J. 2015 Aug;29(8):3124-32. doi: 10.1096/fj.14-266825.
Irene A van Dijk 1 Kamran Nazmi 1 Jan G M Bolscher 1 Enno C I Veerman 1 Jan Stap 2
Affiliations

Affiliations

  • 1 *Department of Oral Biochemistry, Academic Centre for Dentistry Amsterdam, University of Amsterdam and VU University, Amsterdam, The Netherlands; and Core Facility Cellular Imaging, Van Leeuwenhoek Center for Advanced Microscopy, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands.
  • 2 *Department of Oral Biochemistry, Academic Centre for Dentistry Amsterdam, University of Amsterdam and VU University, Amsterdam, The Netherlands; and Core Facility Cellular Imaging, Van Leeuwenhoek Center for Advanced Microscopy, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands j.stap@amc.uva.nl.
Abstract

Histatins (Hsts) are histidine-rich peptides exclusively present in the saliva of higher primates. In this study, we explored the effects of Hsts on cell-substrate and cell-cell adhesion. Histatin (Hst)-1 caused a significant (>2-fold) increase (EC50 = 1 µM) in the ability of human adherent cells to attach and spread, even in conditions that impaired cell spreading. Other tested Hsts did not stimulate cell spreading, indicating a specific effect of Hst1. The effect of Hst1 on cell-cell adhesion was investigated by using transepithelial resistance (TER) measurements in the human cell line Caco-2, a widely used model for the epithelial layer. We found that 10 µM Hst1 caused a 20% increase in TER compared to the negative control, indicating a function for Hst1 in intercellular cell adhesion and epithelial integrity. A role for Hst1 in both cell-substrate and cell-cell adhesion is highly conceivable, because these 2 modes of adhesion are closely related via shared components and connected signaling pathways.

Keywords

barrier function; cell spreading; transepithelial resistance.

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