Literature DB >> 7533785

Migration of bovine aortic smooth muscle cells after wounding injury. The role of hyaluronan and RHAMM.

R C Savani1, C Wang, B Yang, S Zhang, M G Kinsella, T N Wight, R Stern, D M Nance, E A Turley.   

Abstract

The migration of smooth muscle cells is a critical event in the pathogenesis of vascular diseases. We have investigated the role of hyaluronan (HA) and the hyaluronan receptor RHAMM in the migration of adult bovine aortic smooth muscle cells (BASMC). Cultured BASMC migrated from the leading edge of a single scratch wound with increased velocity between 1 and 24 h. Polyclonal anti-RHAMM antisera that block HA binding with this receptor abolished smooth muscle cell migration following injury. HA stimulated the random locomotion of BASMC and its association with the cell monolayer increased following wounding injury. Immunoblot analysis of wounded monolayers demonstrated a novel RHAMM protein isoform that appeared within one hour after injury. At the time of increased cell motility after wounding, FACS analysis demonstrated an increase in the membrane localization in approximately 25% of the cell population. Confocal microscopy of injured monolayers confirmed that membrane expression of this receptor was limited to cells at the wound edge. Collectively, these data demonstrate that RHAMM is necessary for the migration of smooth muscle cells and that expression and distribution of this receptor is tightly regulated following wounding of BASMC monolayers.

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Year:  1995        PMID: 7533785      PMCID: PMC441453          DOI: 10.1172/jci117764

Source DB:  PubMed          Journal:  J Clin Invest        ISSN: 0021-9738            Impact factor:   14.808


  47 in total

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Authors:  T C Laurent; J R Fraser
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5.  Monoclonal antibody to chick embryo hyaluronan-binding protein: changes in distribution of binding protein during early brain development.

Authors:  S D Banerjee; B P Toole
Journal:  Dev Biol       Date:  1991-07       Impact factor: 3.582

6.  Accumulation of hyaluronan and tissue edema in experimental myocardial infarction.

Authors:  A Waldenström; H J Martinussen; B Gerdin; R Hällgren
Journal:  J Clin Invest       Date:  1991-11       Impact factor: 14.808

7.  Proteoglycans in the microvascular. II. Histochemical localization in proliferating capillaries of the rabbit cornea.

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Journal:  Lab Invest       Date:  1991-02       Impact factor: 5.662

9.  Molecular cloning of a novel hyaluronan receptor that mediates tumor cell motility.

Authors:  C Hardwick; K Hoare; R Owens; H P Hohn; M Hook; D Moore; V Cripps; L Austen; D M Nance; E A Turley
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10.  CD44H regulates tumor cell migration on hyaluronate-coated substrate.

Authors:  L Thomas; H R Byers; J Vink; I Stamenkovic
Journal:  J Cell Biol       Date:  1992-08       Impact factor: 10.539

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  53 in total

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Review 4.  Matrix metalloproteinase inhibitors as investigative tools in the pathogenesis and management of vascular disease.

Authors:  Mina M Benjamin; Raouf A Khalil
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Review 5.  Matrix Metalloproteinases, Vascular Remodeling, and Vascular Disease.

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Journal:  Adv Pharmacol       Date:  2017-09-19

Review 6.  Hyaluronan biology: A complex balancing act of structure, function, location and context.

Authors:  Stavros Garantziotis; Rashmin C Savani
Journal:  Matrix Biol       Date:  2019-02-23       Impact factor: 11.583

7.  Atrophin proteins interact with the Fat1 cadherin and regulate migration and orientation in vascular smooth muscle cells.

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8.  Extracellular component hyaluronic acid and its receptor Hmmr are required for epicardial EMT during heart regeneration.

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9.  Organization of hyaluronan and versican in the extracellular matrix of human fibroblasts treated with the viral mimetic poly I:C.

Authors:  Stephen P Evanko; Susan Potter-Perigo; Pamela Y Johnson; Thomas N Wight
Journal:  J Histochem Cytochem       Date:  2009-07-06       Impact factor: 2.479

10.  Blockade of TGF-β by catheter-based local intravascular gene delivery does not alter the in-stent neointimal response, but enhances inflammation in pig coronary arteries.

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Journal:  Int J Cardiol       Date:  2010-01-06       Impact factor: 4.164

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