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      CXCR4 and CXCR7 Mediate TFF3-Induced Cell Migration Independently From the ERK1/2 Signaling Pathway.

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          Abstract

          Trefoil factor family (TFF) peptides, and in particular TFF3, are characteristic secretory products of mucous epithelia that promote antiapoptosis, epithelial migration, restitution, and wound healing. For a long time, a receptor for TFF3 had not yet been identified. However, the chemokine receptor CXCR4 has been described as a low affinity receptor for TFF2. Additionally, CXCR7, which is able to heterodimerize with CXCR4, has also been discussed as a potential TFF2 receptor. Since there are distinct structural similarities between the three known TFF peptides, this study evaluated whether CXCR4 and CXCR7 may also act as putative TFF3 receptors.

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          Author and article information

          Journal
          Invest. Ophthalmol. Vis. Sci.
          Investigative ophthalmology & visual science
          Association for Research in Vision and Ophthalmology (ARVO)
          1552-5783
          0146-0404
          Jan 01 2016
          : 57
          : 1
          Affiliations
          [1 ] Department of Ophthalmology University of Leipzig, Leipzig, Germany 2Department of Anatomy II, Friedrich Alexander University Erlangen-Nürnberg, Erlangen, Germany.
          [2 ] Department of Bioorganic Chemistry, Leibniz Institute of Plant Biochemistry, Halle, Germany.
          [3 ] Institute of Anatomy, Christian Albrecht University of Kiel, Kiel, Germany.
          [4 ] Department of Anatomy II, Friedrich Alexander University Erlangen-Nürnberg, Erlangen, Germany 5Department of Neuroradiology, University of Leipzig, Leipzig, Germany.
          [5 ] Department of Anatomy and Cell Biology, Martin Luther University Halle-Wittenberg, Halle, Germany.
          [6 ] Department of Ophthalmology, Heinrich Heine University Düsseldorf, Düsseldorf, Germany.
          [7 ] Department of Ophthalmology, Ruprecht Karl University Heidelberg, Heidelberg, Germany.
          [8 ] Department of Anatomy II, Friedrich Alexander University Erlangen-Nürnberg, Erlangen, Germany.
          Article
          2482876
          10.1167/iovs.15-18129
          26780310
          416f7134-a52b-4a27-b615-cad13be91dba
          History

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