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Status: Bibliographieeintrag

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Verfasst von:Wagner, Wolfgang [VerfasserIn]   i
 Feldmann, Robert Enrico [VerfasserIn]   i
 Seckinger, Anja [VerfasserIn]   i
 Maurer, Martin H. [VerfasserIn]   i
 Wein, Frederik [VerfasserIn]   i
 Blake, Jonathon [VerfasserIn]   i
 Krause, Ulf [VerfasserIn]   i
 Kalenka, Armin [VerfasserIn]   i
 Bürgers, Heinrich [VerfasserIn]   i
 Saffrich, Rainer [VerfasserIn]   i
 Wuchter, Patrick [VerfasserIn]   i
 Kuschinsky, Wolfgang [VerfasserIn]   i
 Ho, Anthony Dick [VerfasserIn]   i
Titel:The heterogeneity of human mesenchymal stem cell preparations
Titelzusatz:evidence from simultaneous analysis of proteomes and transcriptomes
Verf.angabe:Wolfgang Wagner, Robert E. Feldmann, Anja Seckinger, Martin H. Maurer, Frederik Wein, Jonathon Blake, Ulf Krause, Armin Kalenka, Heinrich F. Bürgers, Rainer Saffrich, Patrick Wuchter, Wolfgang Kuschinsky, and Anthony D. Ho
E-Jahr:2006
Jahr:[2006]
Umfang:13 S.
Fussnoten:Gesehen am 30.04.2021
Titel Quelle:Enthalten in: Experimental hematology
Ort Quelle:Amsterdam [u.a.] : Elsevier Science, 1999
Jahr Quelle:2006
Band/Heft Quelle:34(2006), 4 vom: Apr., Seite 536-548
ISSN Quelle:1873-2399
Abstract:Objective - Mesenchymal stem cells (MSC) raise high hopes in clinical applications. However, the lack of common standards and a precise definition of MSC preparations remains a major obstacle in research and application of MSC. Whereas surface antigen markers have failed to precisely define this population, a combination of proteomic data and microarray data provides a new dimension for the definition of MSC preparations. - Methods - In our continuing effort to characterize MSC, we have analyzed the differential transcriptome and proteome expression profiles of MSC preparations isolated from human bone marrow under two different expansion media (BM-MSC-M1 and BM-MSC-M2). - Results - In proteomics, 136 protein spots were unambiguously identified by MALDI-TOF-MS and corresponding cDNA spots were selected on our “Human Transcriptome cDNA Microarray.” Combination of datasets revealed a correlation in differential gene expression and protein expression of BM-MSC-M1 vs BM-MSC-M2. Genes involved in metabolism were more highly expressed in BM-MSC-M1, whereas genes involved in development, morphogenesis, extracellular matrix, and differentiation were more highly expressed in BM-MSC-M2. Interchanging culture conditions for 8 days revealed that differential expression was retained in several genes whereas it was altered in others. - Conclusion - Our results have provided evidence that homogeneous BM-MSC preparations can reproducibly be isolated under standardized conditions, whereas culture conditions exert a prominent impact on transcriptome, proteome, and cellular organization of BM-MSC.
DOI:doi:10.1016/j.exphem.2006.01.002
URL:Bitte beachten Sie: Dies ist ein Bibliographieeintrag. Ein Volltextzugriff für Mitglieder der Universität besteht hier nur, falls für die entsprechende Zeitschrift/den entsprechenden Sammelband ein Abonnement besteht oder es sich um einen OpenAccess-Titel handelt.

Volltext: https://doi.org/10.1016/j.exphem.2006.01.002
 Volltext: https://www.sciencedirect.com/science/article/pii/S0301472X06000063
 DOI: https://doi.org/10.1016/j.exphem.2006.01.002
Datenträger:Online-Ressource
Sprache:eng
K10plus-PPN:175682231X
Verknüpfungen:→ Zeitschrift

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