Title of article :
Manganese-enhanced magnetic resonance microscopy of mineralization
Author/Authors :
Chesnick، نويسنده , , Ingrid E. and Todorov، نويسنده , , Todor I. and Centeno، نويسنده , , Jose A. and Newbury، نويسنده , , Dale E. and Small، نويسنده , , John A. and Potter، نويسنده , , Kimberlee، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2007
Pages :
10
From page :
1095
To page :
1104
Abstract :
Paramagnetic manganese (II) can be employed as a calcium surrogate to sensitize magnetic resonance microscopy (MRM) to the processing of calcium during bone formation. At high doses, osteoblasts can take up sufficient quantities of manganese, resulting in marked changes in water proton T1, T2 and magnetization transfer ratio values compared to those for untreated cells. Accordingly, inductively coupled plasma mass spectrometry (ICP-MS) results confirm that the manganese content of treated cell pellets was 10-fold higher than that for untreated cell pellets. To establish that manganese is processed like calcium and deposited as bone, calvaria from the skull of embryonic chicks were grown in culture medium supplemented with 1 mM MnCl2 and 3 mM CaCl2. A banding pattern of high and low T2 values, consistent with mineral deposits with high and low levels of manganese, was observed radiating from the calvarial ridge. The results of ICP-MS studies confirm that manganese-treated calvaria take up increasing amounts of manganese with time in culture. Finally, elemental mapping studies with electron probe microanalysis confirmed local variations in the manganese content of bone newly deposited on the calvarial surface. This is the first reported use of manganese-enhanced MRM to study the process whereby calcium is taken up by osteoblasts cells and deposited as bone.
Keywords :
Manganese , Osteoblasts , Magnetic resonance microscopy , mineralization , Calvaria , electron probe microanalysis
Journal title :
Magnetic Resonance Imaging
Serial Year :
2007
Journal title :
Magnetic Resonance Imaging
Record number :
1832584
Link To Document :
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