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Prion Protein at the Leading Edge: Its Role in Cell Motility.
Prado, Mariana Brandão; Melo Escobar, Maria Isabel; Alves, Rodrigo Nunes; Coelho, Bárbara Paranhos; Fernandes, Camila Felix de Lima; Boccacino, Jacqueline Marcia; Iglesia, Rebeca Piatniczka; Lopes, Marilene Hohmuth.
Affiliation
  • Prado MB; Department of Cell and Developmental Biology, Institute of Biomedical Sciences, University of São Paulo, São Paulo 05508-000, Brazil.
  • Melo Escobar MI; Department of Cell and Developmental Biology, Institute of Biomedical Sciences, University of São Paulo, São Paulo 05508-000, Brazil.
  • Alves RN; Department of Cell and Developmental Biology, Institute of Biomedical Sciences, University of São Paulo, São Paulo 05508-000, Brazil.
  • Coelho BP; Department of Cell and Developmental Biology, Institute of Biomedical Sciences, University of São Paulo, São Paulo 05508-000, Brazil.
  • Fernandes CFL; Department of Cell and Developmental Biology, Institute of Biomedical Sciences, University of São Paulo, São Paulo 05508-000, Brazil.
  • Boccacino JM; Department of Cell and Developmental Biology, Institute of Biomedical Sciences, University of São Paulo, São Paulo 05508-000, Brazil.
  • Iglesia RP; Department of Cell and Developmental Biology, Institute of Biomedical Sciences, University of São Paulo, São Paulo 05508-000, Brazil.
  • Lopes MH; Department of Cell and Developmental Biology, Institute of Biomedical Sciences, University of São Paulo, São Paulo 05508-000, Brazil.
Int J Mol Sci ; 21(18)2020 Sep 12.
Article in En | MEDLINE | ID: mdl-32932634
ABSTRACT
Cell motility is a central process involved in fundamental biological phenomena during embryonic development, wound healing, immune surveillance, and cancer spreading. Cell movement is complex and dynamic and requires the coordinated activity of cytoskeletal, membrane, adhesion and extracellular proteins. Cellular prion protein (PrPC) has been implicated in distinct aspects of cell motility, including axonal growth, transendothelial migration, epithelial-mesenchymal transition, formation of lamellipodia, and tumor migration and invasion. The preferential location of PrPC on cell membrane favors its function as a pivotal molecule in cell motile phenotype, being able to serve as a scaffold protein for extracellular matrix proteins, cell surface receptors, and cytoskeletal multiprotein complexes to modulate their activities in cellular movement. Evidence points to PrPC mediating interactions of multiple key elements of cell motility at the intra- and extracellular levels, such as integrins and matrix proteins, also regulating cell adhesion molecule stability and cell adhesion cytoskeleton dynamics. Understanding the molecular mechanisms that govern cell motility is critical for tissue homeostasis, since uncontrolled cell movement results in pathological conditions such as developmental diseases and tumor dissemination. In this review, we discuss the relevant contribution of PrPC in several aspects of cell motility, unveiling new insights into both PrPC function and mechanism in a multifaceted manner either in physiological or pathological contexts.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cell Movement / Prion Proteins Limits: Animals / Humans Language: En Journal: Int J Mol Sci Year: 2020 Document type: Article Affiliation country: Brazil

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cell Movement / Prion Proteins Limits: Animals / Humans Language: En Journal: Int J Mol Sci Year: 2020 Document type: Article Affiliation country: Brazil