P2-069 Quantitative in vivo MR brain imaging in TS65DN mice: a murine model of down's syndrome

2004 ◽  
Vol 25 ◽  
pp. S243
Author(s):  
Victor V. Dyakin ◽  
Yanxin Chen ◽  
Craig A. Branch ◽  
Anne M. Cataldo ◽  
Babak Ardekani ◽  
...  
2000 ◽  
Vol 48 (5) ◽  
pp. 795-798 ◽  
Author(s):  
Domenico Pratic� ◽  
Luigi Iuliano ◽  
Giulia Amerio ◽  
Lina X. Tang ◽  
Joshua Rokach ◽  
...  

Author(s):  
Auxiliadora Sarmiento ◽  
Miguel Ángel Fernández-Granero ◽  
Beatriz Galán ◽  
María Luz Montesinos ◽  
Irene Fondón

Blood ◽  
1985 ◽  
Vol 66 (6) ◽  
pp. 1278-1283
Author(s):  
T Suda ◽  
J Suda ◽  
Y Miura ◽  
Y Hayashi ◽  
M Eguchi ◽  
...  

We present the in vitro differentiation of marrow cells from a patient with Down's syndrome accompanied by megakaryoblastic leukemia into basophils in the presence of phytohemagglutinin-stimulated leukocyte conditioned medium, using a liquid culture and methylcellulose culture system. Identification of basophils was established by metachromatic staining with toluidine blue, transmission electron microscopy, and the presence of histamine. However, these basophils did not release histamine in response to calcium ionophore or chemotactic peptide. Samples from suspension cultures that contained 90% basophils showed chromosomal markers characteristic of leukemic cells (48, XY, +11, +21, t(1;15)) in all examined mitoses. The cellular composition of leukemic colonies grown in methylcellulose culture from single cells was studied using the micromanipulation technique. High plating efficiency and extreme predominance of basophil colonies were observed. In a total 137 cultures, 79 revealed colony growth. Of 59 colonies that were analyzed by cytologic examination, 46 were pure basophil colonies. These basophil colonies showed disperse morphology, similar to that of a normal basophil colony. The clonality of the basophil colonies and skewing of lineage expression were documented from leukemic single-cell cultures. These data showed that leukemic cells have the capacity for differentiation into some lineages that are not expressed in vivo.


2009 ◽  
Vol 40 (4) ◽  
pp. 611-619 ◽  
Author(s):  
F. Beacher ◽  
E. Daly ◽  
A. Simmons ◽  
V. Prasher ◽  
R. Morris ◽  
...  

BackgroundPeople with Down's syndrome (DS) are at high risk for developing dementia in middle age. The biological basis for this is unknown. It has been proposed that non-demented adults with DS may undergo accelerated brain ageing.MethodWe used volumetric magnetic resonance imaging (MRI) and manual tracing to compare brain anatomy and ageing in 39 non-demented adults with DS and 42 healthy controls.ResultsIndividuals with DS had significant differences in brain anatomy. Furthermore, individuals with DS had a significantly greater age-related reduction in volume of frontal, temporal and parietal lobes, and a significantly greater age-related increase in volume of peripheral cerebrospinal fluid (CSF).ConclusionsNon-demented adults with DS have differences in brain anatomy and ‘accelerated’ ageing of some brain regions. This may increase their risk for age-related cognitive decline and Alzheimer's disease (AD).


2003 ◽  
Vol 122 (2) ◽  
pp. 217-225 ◽  
Author(s):  
Sverre O. Lie ◽  
Jonas Abrahamsson ◽  
Niels Clausen ◽  
Erik Forestier ◽  
Henrik Hasle ◽  
...  

2008 ◽  
Vol 39 (4) ◽  
pp. 675-684 ◽  
Author(s):  
F. Beacher ◽  
E. Daly ◽  
A. Simmons ◽  
V. Prasher ◽  
R. Morris ◽  
...  

BackgroundIndividuals with Down's syndrome (DS) are at high risk of developing Alzheimer's disease (AD). However, few studies have investigated brain anatomy in DS individuals with AD.MethodWe compared whole brain anatomy, as measured by volumetric magnetic resonance imaging (MRI), in DS individuals with and without AD. We also investigated whether volumetric differences could reliably classify DS individuals according to AD status. We used volumetric MRI and manual tracing to examine regional brain anatomy in 19 DS adults with AD and 39 DS adults without AD.ResultsDS individuals with AD had significantly smaller corrected volumes bilaterally of the hippocampus and caudate, and right amygdala and putamen, and a significantly larger corrected volume of left peripheral cerebrospinal fluid (CSF), compared to DS individuals without AD. The volume of the hippocampus and caudate nucleus correctly categorized 92% and 92% respectively of DS individuals without AD, and 75% and 80% respectively of DS individuals with AD.ConclusionsDS individuals with AD have significant medial temporal and striatal volume reductions, and these may provide markers of clinical AD.


PLoS ONE ◽  
2013 ◽  
Vol 8 (12) ◽  
pp. e84031 ◽  
Author(s):  
Alexander C. Phillips ◽  
Alison Sleigh ◽  
Catherine J. McAllister ◽  
Soren Brage ◽  
T. Adrian Carpenter ◽  
...  

Author(s):  
Jason P. Lerch ◽  
Lisa Gazdzinski ◽  
Jürgen Germann ◽  
John G. Sled ◽  
R. Mark Henkelman ◽  
...  
Keyword(s):  
Ex Vivo ◽  

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