Document Detail


Proton MR Spectroscopy of Neural Stem Cells: Does the Proton-NMR Peak at 1.28 ppm Function As a Biomarker for Cell Type or State?
MedLine Citation:
PMID:  21548757     Owner:  NLM     Status:  Publisher    
Abstract/OtherAbstract:
Abstract Recently, a peak at 1.28 ppm in proton magnetic resonance spectroscopy ((1)H-MRS) of neural stem cells (NSCs) was introduced as a noninterventional biomarker for neurogenesis in vivo. This would be an urgently needed requisite for translational studies in humans regarding the beneficial role of adult neurogenesis for the structural and functional integrity of the brain. However, many concerns have risen about the validity of the proposed signal as a specific marker for NSCs. The peak has also been related to cell-type-independent phenomena such as apoptosis or necrosis. Thus, we compared the 1.28-ppm peak in various immature stem cell populations, including embryonic stem cells, mouse embryonic fibroblasts, embryonic stem cell- and induced pluripotent stem cell-derived NSCs, ex vivo isolated embryonic NSCs, as well as mature and tumor cell types from different germ layers. To correlate the integral peak intensity with cell death, we induced both apoptosis with camptothecin and necrosis with sodium azide. A peak at 1.28 ppm was found in most cell types, and in most, but not all, NSCH cultures, demonstrating no specificity for NSCs. The intensities of the 1.28-ppm resonance significantly correlated with the rate of apoptosis, but not with the rate of necrosis, cell cycle phase distribution, cell size, or type. Multiple regression analysis displayed a significant predictive value of the peak intensity for apoptosis only. In this context, its specificity for apoptosis as a major selection process during neurogenesis may suggest this resonance as an indirect marker for neurogenesis in vivo.
Authors:
Kai F Loewenbrück; Beate Fuchs; Andreas Hermann; Moritz Brandt; Annett Werner; Matthias Kirsch; Sigrid Schwarz; Johannes Schwarz; Jürgen Schiller; Alexander Storch
Related Documents :
20565897 - Multiple mesodermal lineage differentiation of apodemus sylvaticus embryonic stem cells...
8180967 - Induction of myogenic differentiation in a human rhabdomyosarcoma cell line by phenylac...
18207367 - Roles of autophagy and mtor signaling in neuronal differentiation of mouse neuroblastom...
19559667 - Development of effective isolation method of es cells for analysis of differentiation.
8672987 - Comparison of rectal mucosal proliferation measured by proliferating cell nuclear antig...
10595747 - In vivo cisplatin resistance depending upon canalicular multispecific organic anion tra...
Publication Detail:
Type:  JOURNAL ARTICLE     Date:  2011-5-6
Journal Detail:
Title:  Rejuvenation research     Volume:  -     ISSN:  1557-8577     ISO Abbreviation:  -     Publication Date:  2011 May 
Date Detail:
Created Date:  2011-5-9     Completed Date:  -     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  101213381     Medline TA:  Rejuvenation Res     Country:  -    
Other Details:
Languages:  ENG     Pagination:  -     Citation Subset:  -    
Affiliation:
1 Department of Neurology, Dresden University of Technology , Dresden, Germany .
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


Previous Document:  Low Co-Morbidity, Low Levels of Malnutrition, and Low Risk of Falls in a Community-Dwelling Sample o...
Next Document:  Role of hnRNP-A1 and miR-590-3p in neuronal death: genetics and expression analysis in patients with...