Laminin-511 expression is associated with the functionality of feeder cells in human embryonic stem cell culture |
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Authors: | Hongisto Heidi Vuoristo Sanna Mikhailova Alexandra Suuronen Riitta Virtanen Ismo Otonkoski Timo Skottman Heli |
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Affiliation: | a Regea - Institute for Regenerative Medicine, University of Tampere, Tampere, Finlandb Tampere Graduate Program in Biomedicine and Biotechnology, University of Tampere, Tampere, Finlandc Biomedicum Stem Cell Center, Program of Molecular Neurology, University of Helsinki, Helsinki, Finlandd Hospital for Children and Adolescents, University of Helsinki and Helsinki University Central Hospital, Helsinki, Finlande Department of Biomedical Engineering, Tampere University of Technology, Tampere, Finlandf Department of Eye, Ear and Oral Diseases, Tampere University Hospital, Tampere, Finlandg Department of Anatomy, Institute of Biomedicine, University of Helsinki, Helsinki, Finland |
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Abstract: | Fibroblast feeder cells play an important role in supporting the derivation and long term culture of undifferentiated, pluripotent human embryonic stem cells (hESCs). The feeder cells secrete various growth factors and extracellular matrix (ECM) proteins into extracellular milieu. However, the roles of the feeder cell-secreted factors are largely unclear. Animal feeder cells and use of animal serum also make current feeder cell culture conditions unsuitable for derivation of clinical grade hESCs. We established xeno-free feeder cell lines using human serum (HS) and studied their function in hESC culture. While human foreskin fibroblast (hFF) feeder cells were clearly hESC supportive, none of the established xeno-free human dermal fibroblast (hDF) feeder cells were able to maintain undifferentiated hESC growth. The two fibroblast types were compared for their ECM protein synthesis, integrin receptor expression profiles and key growth factor secretion. We show that hESC supportive feeder cells produce laminin-511 and express laminin-binding integrins α3ß1, α6ß1 and α7ß1. These results indicate specific laminin isoforms and integrins in maintenance of hESC pluripotency in feeder-dependent cultures. In addition, several genes with a known or possible role for hESC pluripotency were differentially expressed in distinct feeder cells. |
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Keywords: | hESC, human embryonic stem cell ECM, extracellular matrix HS, human serum hFF, human foreskin fibroblast hDF, human dermal fibroblast mEF, mouse embryonic fibroblast FBS, fetal bovine serum GMP, good manufacturing practice CM, conditioned medium hiPSC, human induced pluripotent stem cell FGF, fibroblast growth factor TGFß , transforming growth factor beta ActA, activin A KAL1, Kallmann syndrome 1 sequence mESC, mouse embryonic stem cell |
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