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Prion Protein at the Leading Edge: Its Role in Cell Motility.

Mariana Brandão PradoMaria Isabel Melo EscobarRodrigo Nunes AlvesBárbara Paranhos CoelhoCamila Felix de Lima FernandesJacqueline Marcia BoccacinoRebeca Piatniczka IglesiaMarilene Hohmuth Lopes
Published in: International journal of molecular sciences (2020)
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.
Keyphrases
  • single cell
  • cell therapy
  • stem cells
  • biofilm formation
  • public health
  • extracellular matrix
  • spinal cord injury
  • cell adhesion
  • squamous cell carcinoma
  • small molecule
  • signaling pathway
  • escherichia coli
  • candida albicans