LIVIVO - Das Suchportal für Lebenswissenschaften

switch to English language
Erweiterte Suche

Ihre letzten Suchen

  1. AU="Daniell, Esther"
  2. AU="Chou, Chau-Wen"
  3. AU=Kaur Supreet
  4. AU="Yun, Joho"
  5. AU="Tran, Bao G"
  6. AU="Ou Li"
  7. AU="Ting Chen" AU="Ting Chen"
  8. AU="Wilson, Jaymi"
  9. AU="Vane, Christopher H"
  10. AU="Mabbott, Donald"
  11. AU="Martín-Trejo, Jorge Alfonso"
  12. AU=Rieder Hans L

Suchergebnis

Treffer 1 - 2 von insgesamt 2

Suchoptionen

  1. Artikel ; Online: Targeting chondroitinase ABC to axons enhances the ability of chondroitinase to promote neurite outgrowth and sprouting.

    Day, Priscilla / Alves, Nuno / Daniell, Esther / Dasgupta, Debayan / Ogborne, Rosalie / Steeper, Ashley / Raza, Mansoor / Ellis, Clare / Fawcett, James / Keynes, Roger / Muir, Elizabeth

    PloS one

    2020  Band 15, Heft 1, Seite(n) e0221851

    Abstract: Background: There is currently no effective treatment for promoting regeneration of injured nerves in patients who have sustained injury to the central nervous system such as spinal cord injury. Chondroitinase ABC is an enzyme, which promotes neurite ... ...

    Abstract Background: There is currently no effective treatment for promoting regeneration of injured nerves in patients who have sustained injury to the central nervous system such as spinal cord injury. Chondroitinase ABC is an enzyme, which promotes neurite outgrowth and regeneration. It has shown considerable promise as a therapy for these conditions. The aim of the study is to determine if targeting chondroitinase ABC expression to the neuronal axon can further enhance its ability to promote axon outgrowth. Long-distance axon regeneration has not yet been achieved, and would be a significant step in attaining functional recovery following spinal cord injury.
    Methodology/principal findings: To investigate this, neuronal cultures were transfected with constructs encoding axon-targeted chondroitinase, non-targeted chondroitinase or GFP, and the effects on neuron outgrowth and sprouting determined on substrates either permissive or inhibitory to neuron regeneration. The mechanisms underlying the observed effects were also explored. Targeting chondroitinase to the neuronal axon markedly enhances its ability to promote neurite outgrowth. The increase in neurite length is associated with an upregulation of β-integrin staining at the axonal cell surface. Staining for phosphofocal adhesion kinase, is also increased, indicating that the β-integrins are in an activated state. Expression of chondroitinase within the neurons also resulted in a decrease in expression of PTEN and RhoA, molecules which present a block to neurite outgrowth, thus identifying two of the pathways by which ChABC promotes neurite outgrowth.
    Conclusions / significance: The novel finding that targeting ChABC to the axon significantly enhances its ability to promote neurite extension, suggests that this may be an effective way of promoting long-distance axon regeneration following spinal cord injury. It could also potentially improve its efficacy in the treatment of other pathologies, where it has been shown to promote recovery, such as myocardial infarction, stroke and Parkinson's disease.
    Mesh-Begriff(e) Animals ; Axons/metabolism ; Chondroitin ABC Lyase/antagonists & inhibitors ; Chondroitin ABC Lyase/genetics ; Gene Expression Regulation/genetics ; Humans ; Nerve Regeneration/genetics ; Neurites/metabolism ; Neuronal Outgrowth/genetics ; Neurons/metabolism ; Neurons/physiology ; PTEN Phosphohydrolase/genetics ; Recovery of Function/genetics ; Spinal Cord Injuries/genetics ; Spinal Cord Injuries/physiopathology ; Spinal Cord Injuries/therapy ; rhoA GTP-Binding Protein/genetics
    Chemische Substanzen PTEN Phosphohydrolase (EC 3.1.3.67) ; rhoA GTP-Binding Protein (EC 3.6.5.2) ; Chondroitin ABC Lyase (EC 4.2.2.20)
    Sprache Englisch
    Erscheinungsdatum 2020-01-21
    Erscheinungsland United States
    Dokumenttyp Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2267670-3
    ISSN 1932-6203 ; 1932-6203
    ISSN (online) 1932-6203
    ISSN 1932-6203
    DOI 10.1371/journal.pone.0221851
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

    Zusatzmaterialien

    Kategorien

  2. Artikel ; Online: Trafficking and processing of bacterial proteins by mammalian cells: Insights from chondroitinase ABC.

    Muir, Elizabeth / Raza, Mansoor / Ellis, Clare / Burnside, Emily / Love, Fiona / Heller, Simon / Elliot, Matthew / Daniell, Esther / Dasgupta, Debayan / Alves, Nuno / Day, Priscilla / Fawcett, James / Keynes, Roger

    PloS one

    2017  Band 12, Heft 11, Seite(n) e0186759

    Abstract: Background: There is very little reported in the literature about the relationship between modifications of bacterial proteins and their secretion by mammalian cells that synthesize them. We previously reported that the secretion of the bacterial enzyme ...

    Abstract Background: There is very little reported in the literature about the relationship between modifications of bacterial proteins and their secretion by mammalian cells that synthesize them. We previously reported that the secretion of the bacterial enzyme Chondroitinase ABC by mammalian cells requires the strategic removal of at least three N-glycosylation sites. The aim of this study was to determine if it is possible to enhance the efficacy of the enzyme as a treatment for spinal cord injury by increasing the quantity of enzyme secreted or by altering its cellular location.
    Methodology/principal findings: To determine if the efficiency of enzyme secretion could be further increased, cells were transfected with constructs encoding the gene for chondroitinase ABC modified for expression by mammalian cells; these contained additional modifications of strategic N-glycosylation sites or alternative signal sequences to direct secretion of the enzyme from the cells. We show that while removal of certain specific N-glycosylation sites enhances enzyme secretion, N-glycosylation of at least two other sites, N-856 and N-773, is essential for both production and secretion of active enzyme. Furthermore, we find that the signal sequence directing secretion also influences the quantity of enzyme secreted, and that this varies widely amongst the cell types tested. Last, we find that replacing the 3'UTR on the cDNA encoding Chondroitinase ABC with that of β-actin is sufficient to target the enzyme to the neuronal growth cone when transfected into neurons. This also enhances neurite outgrowth on an inhibitory substrate.
    Conclusion/significance: Some intracellular trafficking pathways are adversely affected by cryptic signals present in the bacterial gene sequence, whilst unexpectedly others are required for efficient secretion of the enzyme. Furthermore, targeting chondroitinase to the neuronal growth cone promotes its ability to increase neurite outgrowth on an inhibitory substrate. These findings are timely in view of the renewed prospects for gene therapy, and of direct relevance to strategies aimed at expressing foreign proteins in mammalian cells, in particular bacterial proteins.
    Mesh-Begriff(e) 3' Untranslated Regions/genetics ; Actins/genetics ; Animals ; Bacterial Proteins/metabolism ; Cell Line ; Chondroitin ABC Lyase/metabolism ; Dogs ; Female ; Fluorescence ; Glycosylation ; Growth Cones/metabolism ; Humans ; Mammals ; Neurites/metabolism ; Protein Processing, Post-Translational ; Protein Sorting Signals ; Protein Transport ; Rats ; Substrate Specificity ; Transfection
    Chemische Substanzen 3' Untranslated Regions ; Actins ; Bacterial Proteins ; Protein Sorting Signals ; Chondroitin ABC Lyase (EC 4.2.2.20)
    Sprache Englisch
    Erscheinungsdatum 2017-11-09
    Erscheinungsland United States
    Dokumenttyp Journal Article
    ZDB-ID 2267670-3
    ISSN 1932-6203 ; 1932-6203
    ISSN (online) 1932-6203
    ISSN 1932-6203
    DOI 10.1371/journal.pone.0186759
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

    Zusatzmaterialien

    Kategorien

Zum Seitenanfang