|Title||RNA-seq analysis reveals different dynamics of differentiation of human dermis- and adipose-derived stromal stem cells.|
|Publication Type||Journal Article|
|Year of Publication||2012|
|Authors||Jääger K, Islam S, Zajac P, Linnarsson S, Neuman T|
|Keywords||Adipogenesis, Adipose Tissue, Cell Differentiation, Cells, Cultured, Chondrocytes, Dermis, Fibroblasts, Gene Expression Profiling, Gene Expression Regulation, Humans, Mesenchymal Stromal Cells, Organ Specificity, Osteogenesis, Sequence Analysis, RNA, Transcriptome|
BACKGROUND: Tissue regeneration and recovery in the adult body depends on self-renewal and differentiation of stem and progenitor cells. Mesenchymal stem cells (MSCs) that have the ability to differentiate into various cell types, have been isolated from the stromal fraction of virtually all tissues. However, little is known about the true identity of MSCs. MSC populations exhibit great tissue-, location- and patient-specific variation in gene expression and are heterogeneous in cell composition.
METHODOLOGY/PRINCIPAL FINDINGS: Our aim was to analyze the dynamics of differentiation of two closely related stromal cell types, adipose tissue-derived MSCs (AdMSCs) and dermal fibroblasts (FBs) along adipogenic, osteogenic and chondrogenic lineages using multiplex RNA-seq technology. We found that undifferentiated donor-matched AdMSCs and FBs are distinct populations that stay different upon differentiation into adipocytes, osteoblasts and chondrocytes. The changes in lineage-specific gene expression occur early in differentiation and persist over time in both AdMSCs and FBs. Further, AdMSCs and FBs exhibit similar dynamics of adipogenic and osteogenic differentiation but different dynamics of chondrogenic differentiation.
CONCLUSIONS/SIGNIFICANCE: Our findings suggest that stromal stem cells including AdMSCs and dermal FBs exploit different molecular mechanisms of differentiation to reach a common cell fate. The early mechanisms of differentiation are lineage-specific and are similar for adipogenic and osteogenic differentiation but are distinct for chondrogenic differentiation between AdMSCs and FBs.
|Alternate Journal||PLoS ONE|
|PubMed Central ID||PMC3378616|