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Human-serum matrix supports undifferentiated growth of human embryonic stem cells.
- Source :
-
Stem cells (Dayton, Ohio) [Stem Cells] 2005 Aug; Vol. 23 (7), pp. 895-902. Date of Electronic Publication: 2005 May 11. - Publication Year :
- 2005
-
Abstract
- One of the most frequently used matrices for feeder-free growth of undifferentiated human embryonic stem cells (hESCs) is Matrigel, which supports attachment and growth of undifferentiated hESCs in the presence of mouse embryonic fibroblast-conditioned medium. Unfortunately, application of Matrigel or medium conditioned by mouse embryonic feeder cells is not ideal for potential medical application of hESCs because xenogeneic pathogens can be transmitted through culture conditions. We demonstrate here that human serum as matrix and medium conditioned by differentiated hESCs reduce exposure of hESCs to animal ingredients and provide a safer direction toward completely animal-free conditions for application, handling, and understanding of hESC biology. At the same time, hESCs grown under these conditions maintain all hESC features after prolonged culture, including the developmental potential to differentiate into representative tissues of all three embryonic germ layers, unlimited and undifferentiated proliferative ability, and maintenance of normal karyotype.
- Subjects :
- Animals
Cell Culture Techniques instrumentation
Cell Differentiation
Cell Proliferation
Collagen pharmacology
Culture Media, Conditioned pharmacology
DNA Primers chemistry
Drug Combinations
Humans
Karyotyping methods
Laminin pharmacology
Male
Mice
Mice, SCID
Microscopy, Electron, Scanning
Proteoglycans pharmacology
Reverse Transcriptase Polymerase Chain Reaction
Testis metabolism
Cell Culture Techniques methods
Embryo, Mammalian cytology
Serum metabolism
Stem Cells cytology
Subjects
Details
- Language :
- English
- ISSN :
- 1066-5099
- Volume :
- 23
- Issue :
- 7
- Database :
- MEDLINE
- Journal :
- Stem cells (Dayton, Ohio)
- Publication Type :
- Academic Journal
- Accession number :
- 15888688
- Full Text :
- https://doi.org/10.1634/stemcells.2004-0326