Abstract

Stromal cells have been widely used in biomedical research and disease modeling studies in vitro. The most commonly used types of stromal cells are mesenchymal stem cells and fibroblasts. Their cellular phenotypes and differentiation capabilities are quite similar and there are no specific distinction criteria. In order to identify transcriptomic differences between these 2 cell types, we performed next-generation RNA sequencing. Using the global gene expression profile and pathway analysis, we showed that human primary bone marrow mesenchymal stem cells and human primary dermal fibroblasts have different molecular signatures. We also identified critical transcription factors that are differentially expressed between these cells. We then proposed that homeobox genes and some other sequence-specific transcription factors are not only responsible for transcriptional differences, but also discriminate bone marrow mesenchymal stem cells and dermal fibroblasts at the transcriptional level.

Highlights

  • Stromal cells have been widely used in biomedical research and disease modeling studies in vitro

  • The aim of this study is to reveal the transcriptomic profiles of human BM-mesenchymal stem/stromal cell (MSC) and dermal fibroblast (DF) in order to identify discriminating markers

  • We found that 419 and 773 genes were upregulated in Human Primary Bone marrow mesenchymal stem/stromal cells (BM-MSCs) and in Human Primary DFs, respectively

Read more

Summary

Introduction

Stromal cells have been widely used in biomedical research and disease modeling studies in vitro. Bone marrow mesenchymal stem/stromal cells (BM-MSCs) are positive for specific surface markers CD90, CD73, and CD105 and negative for specific surface markers CD45, CD34, CD14, and CD19 according to the International Society for Cellular Therapy (ISCT) (Bae, 2009; Charbord, 2010; Pontikoglou, 2011). They are spindle-shaped adherent cells and have the capacity to differentiate into cell types of this lineage such as adipocyte, osteocyte, chondrocyte, myocyte, tendocyte, and ligamentocyte (Pontikoglou, 2011). These features make MSCs very advantageous for regenerative medicine and therapeutic approaches

Objectives
Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call