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Albumin targeting of damaged muscle fibres in the mdx mouse can be monitored by MRI
Authors:Amthor Helge  Egelhof Thomas  McKinnell Iain  Ladd Mark E  Janssen Isabelle  Weber Johannes  Sinn Hannsjörg  Schrenk Hans-Hermann  Forsting Michael  Voit Thomas  Straub Volker
Affiliation:

aDepartment of Paediatrics and Paediatric Neurology, University Hospital of Essen, Hufelandstrasse 55, Essen D-45122, Germany

bDepartment of Diagnostic and Interventional Radiology, University Hospital of Essen, Hufelandstrasse 55, Essen D-45122, Germany

cDepartment of Veterinary Basic Sciences, Royal Veterinary College, Royal College Street, London NW1 OTU, England

dGerman Cancer Research Center, Department of Radiochemistry, Im Neuenheimer Feld, Heidelberg 69122, Germany

eRösner Research, Im Neuenheimer Feld 582, Heidelberg 69120, Germany

Abstract:Increased sarcolemmal permeability has been implicated as a major pathological event in muscular dystrophies. In our study, we evaluated whether damaged muscle fibres can be specifically targeted using albumin as a carrier. We tagged human serum albumin (HSA) with Gadolinium (Gd) and systemically applied this compound (Gd-DTPA-HSA) to wildtype and dystrophin-deficient mdx mice. We performed magnetic resonance imaging before and after intravenous administration of Gd-DTPA-HSA and found localised signal enhancement only in mdx skeletal muscle. We also examined skeletal muscle after contrast enhanced magnetic resonance imaging using anti-human albumin antibodies and demonstrated intracellular accumulation of Gd-DTPA-HSA in clusters of damaged mdx muscle fibres. Comparison of magnetic resonance imaging and histological data emphasised the value of contrast agent enhanced magnetic resonance imaging for the in vivo assessment of fibre damage in muscular dystrophies. Furthermore, our data provide evidence that albumin can be used as a carrier to target covalently bound molecules to degenerating muscle fibres.
Keywords:Muscular dystrophy   DMD   mdx   MRI   Gd-DTPA   Serum albumin
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