Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2010 Dec;6(4):532-47.
doi: 10.1007/s12015-010-9180-z.

In Silico Analyses of Proteomic Data Suggest a Role for Heat Shock Proteins in Umbilical Cord Blood Hematopoietic Stem Cells

Affiliations

In Silico Analyses of Proteomic Data Suggest a Role for Heat Shock Proteins in Umbilical Cord Blood Hematopoietic Stem Cells

Angelo D'Alessandro et al. Stem Cell Rev Rep. .

Abstract

Umbilical-cord blood (UCB) has growingly become an accepted alternative source of hematopoietic stem cells for transplantation purposes. However, the low cell dose limit within a single unit is still an obstacle hindering the way of a broader diffusion. The real deal is the lack of knowledge about the molecular processes governing the events of expansion and differentiation of these cells. In order to fill this void, several studies were focused on the identification of the peculiar whole protein profile of UCB-derived hematopoietic stem cells. In this review article we provide a referenced list of overall proteins from UCB-derived hematopoietic stem and progenitor cells. This list has been elaborated for pathway and network analyses, along with GO term enrichment for biological and molecular functions, in order to individuate main classes of proteins governing functioning of these cells. From these analyses it seems to emerge a central role for heat shock proteins in immature hematopoietic stem cells. Their role might be relevant in protecting crucial transcription factors which drive proliferation and differentiation towards a specific lineage (e.g. erythroid, myeloid). Hereby we also stress the helpfulness of interactomics elaboration in providing a unified overview of independent proteomics data. It appears that maturation, other than representing a bottleneck to protein expression, could sculpt interaction maps via reducing complexity of immature interactomics profiles.

Similar articles

See all similar articles

Cited by 3 articles

References

    1. Immunology. 1999 Jun;97(2):226-31 - PubMed
    1. Cell Death Differ. 2003 Jun;10(6):619-20 - PubMed
    1. Nucleic Acids Res. 2003 Jan 1;31(1):315-8 - PubMed
    1. J Proteome Res. 2010 Jan;9(1):144-63 - PubMed
    1. Blood. 2003 Jun 15;101(12):5061-7 - PubMed

MeSH terms

LinkOut - more resources

Feedback