Phosphoinositide 3-kinases and regulation of embryonic stem cell fate

被引:28
作者
Welham, M. J. [1 ]
Storm, M. P.
Kingham, E.
Bone, H. K.
机构
[1] Univ Bath, Dept Pharm & Pharmacol, Bath BA2 7AY, Avon, England
[2] Univ Bath, Ctr Regenerat Med, Bath BA2 7AY, Avon, England
基金
英国惠康基金;
关键词
bone morphogenetic protein (BMP); embryonic stem cell (ES cell); phosphoinositide 3-kinase (PI3K); plunpotency; self-renewal;
D O I
10.1042/BST0350225
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
ES (embryonic stem) cell lines are derived from the epiblast of pre-implantation embryos and like the inner cell mass cells from which they are derived exhibit the remarkable property of pluripotency, namely the ability to differentiate into all cell lineages comprising the adult organism. ES cells and their differentiated progeny offer tremendous potential to regenerative medicine, particularly as cellular therapies for the treatment of a wide variety of chronic disorders, such as Type 1 diabetes, Parkinson's disease and retinal degeneration. In order for this potential to be realized, a detailed understanding of the molecular mechanisms regulating the fundamental properties of ES cells, i.e. pluripotency, proliferation and differentiation, is required. In the present paper, we review the evidence that PI3K (phosphoinositide 3-kinase)-dependent signalling plays a role in regulation of both ES cell pluripotency and proliferation.
引用
收藏
页码:225 / 228
页数:4
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