TY - JOUR
T1 - Regional differences in expression of specific markers for human embryonic stem cells
AU - Laursen, Steen B
AU - Møllgård, Kjeld
AU - Olesen, Christian
AU - Oliveri, Roberto S
AU - Brøchner, Christian B
AU - Byskov, Anne Grete
AU - Andersen, Anders Nyboe
AU - Høyer, Poul Erik
AU - Tommerup, Niels
AU - Yding Andersen, Claus
PY - 2007/7
Y1 - 2007/7
N2 - Characterization of human embryonic stem cell (hESC) lines derived from the inner cell masses of blastocysts generally includes expression analysis of markers such as OCT4, NANOG, SSEA3, SSEA4, TRA-1-60 and TRA-1-81. Expression is usually detected by immunocytochemical staining of entire colonies of hESC, using one colony for each individual marker. Four newly established hESC lines showed the expected expression pattern and were capable of differentiating into the three germ layers in vitro. Neighbouring sections of entire colonies grown for 4, 11, 21 and 28 days respectively were stained with different markers to study the regional distribution and cellular co-expression. TRA-1-60 staining defined the hESC territory at all time points analysed. This territory comprised a characteristic OCT4 and NANOG staining often in overlapping subregions. Staining intensity of nuclei varied from strong OCT4 staining to weak or absent NANOG staining, and vice versa. SSEA4 staining was only observed in small clusters or single cells and not confined to the TRA territory. Co-expression of all markers was only detected in small areas. SSEA1 expression was found exclusively outside the TRA territory. In conclusion, pronounced regional differences in the expression of markers considered specific for undifferentiated hESC may suggest the existence of different cell populations.
AB - Characterization of human embryonic stem cell (hESC) lines derived from the inner cell masses of blastocysts generally includes expression analysis of markers such as OCT4, NANOG, SSEA3, SSEA4, TRA-1-60 and TRA-1-81. Expression is usually detected by immunocytochemical staining of entire colonies of hESC, using one colony for each individual marker. Four newly established hESC lines showed the expected expression pattern and were capable of differentiating into the three germ layers in vitro. Neighbouring sections of entire colonies grown for 4, 11, 21 and 28 days respectively were stained with different markers to study the regional distribution and cellular co-expression. TRA-1-60 staining defined the hESC territory at all time points analysed. This territory comprised a characteristic OCT4 and NANOG staining often in overlapping subregions. Staining intensity of nuclei varied from strong OCT4 staining to weak or absent NANOG staining, and vice versa. SSEA4 staining was only observed in small clusters or single cells and not confined to the TRA territory. Co-expression of all markers was only detected in small areas. SSEA1 expression was found exclusively outside the TRA territory. In conclusion, pronounced regional differences in the expression of markers considered specific for undifferentiated hESC may suggest the existence of different cell populations.
KW - Antigens, Surface/genetics
KW - Antigens, Tumor-Associated, Carbohydrate/genetics
KW - Biomarkers/metabolism
KW - Cell Line
KW - Cell Lineage
KW - DNA-Binding Proteins/genetics
KW - Embryonic Stem Cells/cytology
KW - Glycosphingolipids/genetics
KW - Homeodomain Proteins/genetics
KW - Humans
KW - Immunohistochemistry
KW - Lewis X Antigen/genetics
KW - Nanog Homeobox Protein
KW - Octamer Transcription Factor-3/genetics
KW - Proteoglycans/genetics
KW - Reverse Transcriptase Polymerase Chain Reaction
KW - Stage-Specific Embryonic Antigens
U2 - 10.1016/s1472-6483(10)60697-9
DO - 10.1016/s1472-6483(10)60697-9
M3 - Journal article
C2 - 17623545
SN - 1472-6483
VL - 15
SP - 89
EP - 98
JO - Reproductive BioMedicine Online
JF - Reproductive BioMedicine Online
IS - 1
ER -