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Signaling networks regulating leukocyte podosome dynamics and function
Authors:Dovas Athanassios  Cox Dianne
Institution:
  • a Department of Anatomy & Structural Biology, Albert Einstein College of Medicine, Bronx, NY, 10461, USA
  • b Department of Developmental & Molecular Biology, Albert Einstein College of Medicine, Bronx, NY, 10461, USA
  • Abstract:Podosomes are ventral adhesion structures prominent in cells of the myeloid lineage. A common aspect of these cells is that they are highly motile and must to traverse multiple tissue barriers in order to perform their functions. Recently podosomes have gathered attention from researchers as important cellular structures that can influence cell adhesion, motility and matrix remodeling. Adhesive and soluble ligands act via transmembrane receptors and propagate signals to the leukocyte cytoskeleton via small G proteins of the Rho family, tyrosine kinases and scaffold proteins and are able to induce podosome formation and rearrangements. Manipulation of the signals that regulate podosome formation and dynamics can therefore be a strategy to interfere with leukocyte functions in a multitude of pathological settings, such as infections, atherosclerosis and arthritis. Here, we review the major signaling molecules that act in the formation and regulation of podosomes.
    Keywords:BMM  bone marrow-derived macrophage  DC  dendritic cell  CIP4  Cdc42 interacting protein 4  CSF-1(R)  colony stimulating factor-1(receptor)  GAP  GTPase activating protein  GDI  guanine nucleotide dissociation inhibitor  LPS  lipopolysaccharide  mDia  mammalian Diaphanous  (MT1)MMP  (membrane type 1) matrix metalloprotease  PAK  p21 associated kinase  PGE2  prostaglandin E2  PSTPIP  proline  serine  threonine phosphatase interacting protein  PKC  protein kinase C  PLC  phospholipase C  ROCK  Rho associated kinase  WASP  Wiskott-Aldrich Syndrome protein  WIP  WASP interacting protein
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