HUMAN ADIPOSE-TISSUE;
MINERALIZATION IN-VITRO;
INHIBIT BONE-FORMATION;
OSTEOBLAST-LIKE CELLS;
UMBILICAL-CORD BLOOD;
EXTRACELLULAR NUCLEOTIDES;
INTRACELLULAR CALCIUM;
NEURONAL DIFFERENTIATION;
LYSOPHOSPHATIDIC ACID;
INTERNATIONAL UNION;
D O I:
10.1089/scd.2010.0576
中图分类号:
Q813 [细胞工程];
学科分类号:
100113 [医学细胞生物学];
摘要:
Adult stem cells, including adipose tissue-derived mesenchymal stem cells (MSCs) or ectomesenchymal dental follicle cells (DFCs), attract considerable attention for their potential to differentiate into lineages, which are of major interest in the field of Regenerative Medicine. Purinergic receptors exert a wide range of biological actions in many cell and tissue types through extracellular nucleotides. Little is known about P2 receptors in adult stem cells and changes in their expression levels during differentiation. All known P2 receptors have been investigated, and a variety of P2X and P2Y receptor subtypes were detected in MSCs. Studies investigating intracellular calcium levels on receptor stimulation demonstrated that the found P2 receptors are metabolically active. Interestingly, up- or downregulation of several P2 receptor subtypes at gene and protein level was observed during adipogenic and osteogenic differentiation, and the effect on differentiation was directly influenced by both the application of agonists/antagonists and apyrase-induced nucleotide cleavage. Here, we show for the first time that the combination of several P2 receptors plays a role in the differentiation of adult stem cells. The expression pattern of the P2 receptors, as well as their fate in differentiation, varies in stem cells of mesenchymal origin if compared with stem cells of ectomesenchymal origin. The subtypes P2X6, P2Y4, and P2Y14 seem to be pivotal regulators in MSC commitment, as they are regulated in both adipogenic and osteogenic differentiation of adipose tissue-derived stem cells and DFCs. These findings provide new insights into the differentiation processes and might reveal novel options to influence stem cell fate in future applications.
机构:
Univ Liverpool, Dept Human Anat & Cell Biol, Human Bone Cell Res Grp, Liverpool L69 3GE, Merseyside, EnglandUniv Liverpool, Dept Human Anat & Cell Biol, Human Bone Cell Res Grp, Liverpool L69 3GE, Merseyside, England
Bowler, WB
;
Buckley, KA
论文数: 0引用数: 0
h-index: 0
机构:Univ Liverpool, Dept Human Anat & Cell Biol, Human Bone Cell Res Grp, Liverpool L69 3GE, Merseyside, England
Buckley, KA
;
论文数: 引用数:
h-index:
机构:
Gartland, A
;
Hipskind, RA
论文数: 0引用数: 0
h-index: 0
机构:Univ Liverpool, Dept Human Anat & Cell Biol, Human Bone Cell Res Grp, Liverpool L69 3GE, Merseyside, England
Hipskind, RA
;
Bilbe, G
论文数: 0引用数: 0
h-index: 0
机构:Univ Liverpool, Dept Human Anat & Cell Biol, Human Bone Cell Res Grp, Liverpool L69 3GE, Merseyside, England
机构:
UCL Royal Free & Univ Coll, Med Sch, Autonom Neurosci Ctr, London NWS 2PF, EnglandUCL Royal Free & Univ Coll, Med Sch, Autonom Neurosci Ctr, London NWS 2PF, England
机构:
Univ Liverpool, Dept Human Anat & Cell Biol, Human Bone Cell Res Grp, Liverpool L69 3GE, Merseyside, EnglandUniv Liverpool, Dept Human Anat & Cell Biol, Human Bone Cell Res Grp, Liverpool L69 3GE, Merseyside, England
Bowler, WB
;
Buckley, KA
论文数: 0引用数: 0
h-index: 0
机构:Univ Liverpool, Dept Human Anat & Cell Biol, Human Bone Cell Res Grp, Liverpool L69 3GE, Merseyside, England
Buckley, KA
;
论文数: 引用数:
h-index:
机构:
Gartland, A
;
Hipskind, RA
论文数: 0引用数: 0
h-index: 0
机构:Univ Liverpool, Dept Human Anat & Cell Biol, Human Bone Cell Res Grp, Liverpool L69 3GE, Merseyside, England
Hipskind, RA
;
Bilbe, G
论文数: 0引用数: 0
h-index: 0
机构:Univ Liverpool, Dept Human Anat & Cell Biol, Human Bone Cell Res Grp, Liverpool L69 3GE, Merseyside, England
机构:
UCL Royal Free & Univ Coll, Med Sch, Autonom Neurosci Ctr, London NWS 2PF, EnglandUCL Royal Free & Univ Coll, Med Sch, Autonom Neurosci Ctr, London NWS 2PF, England