4.8 Article

Regulatory networks define phenotypic classes of human stem cell lines

期刊

NATURE
卷 455, 期 7211, 页码 401-U55

出版社

NATURE PUBLISHING GROUP
DOI: 10.1038/nature07213

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资金

  1. Christian- Abrechts University Young Investigator Award
  2. Hamburger Krebsgesellschaft Grant
  3. Edmond J. Safra Bioinformatics program fellowship at Tel- Aviv University (I.U.)
  4. Converging Technologies Program of The Israel Science Foundation [1767.07]
  5. Raymond and Beverly Sackler Chair in Bioinformatics
  6. Reproductive Scientist Development Program Scholar Award [K12 5K12HD000849-20]
  7. California Institute for Regenerative Medicine Clinical Scholar Award [NIH P20 GM075059-01]
  8. Alzheimer's Association
  9. [SFB-654/C5]

向作者/读者索取更多资源

Stem cells are defined as self- renewing cell populations that can differentiate into multiple distinct cell types. However, hundreds of different human cell lines from embryonic, fetal and adult sources have been called stem cells, even though they range from pluripotent cells - typified by embryonic stem cells, which are capable of virtually unlimited proliferation and differentiation - to adult stem cell lines, which can generate a far more limited repertoire of differentiated cell types. The rapid increase in reports of new sources of stem cells and their anticipated value to regenerative medicine(1,2) has highlighted the need for a general, reproducible method for classification of these cells(3). We report here the creation and analysis of a database of global gene expression profiles ( which we call the 'stem cell matrix') that enables the classification of cultured human stem cells in the context of a wide variety of pluripotent, multipotent and differentiated cell types. Using an unsupervised clustering method(4,5) to categorize a collection of similar to 150 cell samples, we discovered that pluripotent stem cell lines group together, whereas other cell types, including brain-derived neural stem cell lines, are very diverse. Using further bioinformatic analysis(6) we uncovered a protein - protein network (PluriNet) that is shared by the pluripotent cells ( embryonic stem cells, embryonal carcinomas and induced pluripotent cells). Analysis of published data showed that the PluriNet seems to be a common characteristic of pluripotent cells, including mouse embryonic stem and induced pluripotent cells and human oocytes. Our results offer a new strategy for classifying stem cells and support the idea that pluripotency and self- renewal are under tight control by specific molecular networks.

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