TY - JOUR
T1 - Human placenta-derived cells have mesenchymal stem/progenitor cell potential
AU - Fukuchi, Yumi
AU - Nakajima, Hideaki
AU - Sugiyama, Daisuke
AU - Hirose, Imiko
AU - Kitamura, Toshio
AU - Tsuji, Kohichiro
PY - 2004
Y1 - 2004
N2 - Mesenchymal stem/progenitor cells (MSCs) are widely distributed in a variety of tissues in the adult human body (e.g., bone marrow [BM], kidney, lung, and liver). These cells are also present in the fetal environment (e.g., blood, liver, BM, and kidney). However, MSCs are a rare population in these tissues. Here we tried to identify cells with MSC-like potency in human placenta. We isolated adherent cells from trypsin-digested term placentas and established two clones by limiting dilution. We examined these cells for morphology, surface markers, gene expression patterns, and differentiation potential and found that they expressed several stem cell markers, hematopoietic/endothelial cell-related genes, and organ-specific genes, as determined by reverse transcription- polymerase chain reaction and fluorescence-activated cell sorter analysis. They also showed osteogenic and adipogenic differentiation potentials under appropriate conditions. We suggest that placenta-derived cells have multilineage differentiation potential similar to MSCs in terms of morphology, cell-surface antigen expression, and gene expression patterns. The placenta may prove to be a useful source of MSCs.
AB - Mesenchymal stem/progenitor cells (MSCs) are widely distributed in a variety of tissues in the adult human body (e.g., bone marrow [BM], kidney, lung, and liver). These cells are also present in the fetal environment (e.g., blood, liver, BM, and kidney). However, MSCs are a rare population in these tissues. Here we tried to identify cells with MSC-like potency in human placenta. We isolated adherent cells from trypsin-digested term placentas and established two clones by limiting dilution. We examined these cells for morphology, surface markers, gene expression patterns, and differentiation potential and found that they expressed several stem cell markers, hematopoietic/endothelial cell-related genes, and organ-specific genes, as determined by reverse transcription- polymerase chain reaction and fluorescence-activated cell sorter analysis. They also showed osteogenic and adipogenic differentiation potentials under appropriate conditions. We suggest that placenta-derived cells have multilineage differentiation potential similar to MSCs in terms of morphology, cell-surface antigen expression, and gene expression patterns. The placenta may prove to be a useful source of MSCs.
KW - Cell culture
KW - Human placenta
KW - Mesenchymal stem/progenitor cells
KW - Placenta-derived cells
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U2 - 10.1634/stemcells.22-5-649
DO - 10.1634/stemcells.22-5-649
M3 - Article
C2 - 15342929
AN - SCOPUS:4444300615
SN - 1066-5099
VL - 22
SP - 649
EP - 658
JO - International Journal of Cell Cloning
JF - International Journal of Cell Cloning
IS - 5
ER -