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High-depth transcriptomic profiling reveals the temporal gene signature of human mesenchymal stem cells during chondrogenesis.

Publication ,  Journal Article
Huynh, NPT; Zhang, B; Guilak, F
Published in: FASEB journal : official publication of the Federation of American Societies for Experimental Biology
January 2019

Mesenchymal stem/stromal cells (MSCs) provide an attractive cell source for cartilage repair and cell therapy; however, the underlying molecular pathways that drive chondrogenesis of these populations of adult stem cells remain poorly understood. We generated a rich data set of high-throughput RNA sequencing of human MSCs throughout chondrogenesis at 6 different time points. Our data consisted of 18 libraries with 3 individual donors as biologic replicates, with each library possessing a sequencing depth of 100 million reads. Computational analyses with differential gene expression, gene ontology, and weighted gene correlation network analysis identified dynamic changes in multiple biologic pathways and, most importantly, a chondrogenic gene subset, whose functional characterization promises to further harness the potential of MSCs for cartilage tissue engineering. Furthermore, we created a graphic user interface encyclopedia built with the goal of producing an open resource of transcriptomic regulation for additional data mining and pathway analysis of the process of MSC chondrogenesis.-Huynh, N. P. T., Zhang, B., Guilak, F. High-depth transcriptomic profiling reveals the temporal gene signature of human mesenchymal stem cells during chondrogenesis.

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Published In

FASEB journal : official publication of the Federation of American Societies for Experimental Biology

DOI

EISSN

1530-6860

ISSN

0892-6638

Publication Date

January 2019

Volume

33

Issue

1

Start / End Page

358 / 372

Related Subject Headings

  • Tissue Engineering
  • Signal Transduction
  • Mesenchymal Stem Cells
  • Humans
  • High-Throughput Nucleotide Sequencing
  • Gene Regulatory Networks
  • Gene Expression Profiling
  • Chondrocytes
  • Cells, Cultured
  • Cell Differentiation
 

Citation

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Huynh, N. P. T., Zhang, B., & Guilak, F. (2019). High-depth transcriptomic profiling reveals the temporal gene signature of human mesenchymal stem cells during chondrogenesis. FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology, 33(1), 358–372. https://doi.org/10.1096/fj.201800534r
Huynh, Nguyen P. T., Bo Zhang, and Farshid Guilak. “High-depth transcriptomic profiling reveals the temporal gene signature of human mesenchymal stem cells during chondrogenesis.FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology 33, no. 1 (January 2019): 358–72. https://doi.org/10.1096/fj.201800534r.
Huynh NPT, Zhang B, Guilak F. High-depth transcriptomic profiling reveals the temporal gene signature of human mesenchymal stem cells during chondrogenesis. FASEB journal : official publication of the Federation of American Societies for Experimental Biology. 2019 Jan;33(1):358–72.
Huynh, Nguyen P. T., et al. “High-depth transcriptomic profiling reveals the temporal gene signature of human mesenchymal stem cells during chondrogenesis.FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology, vol. 33, no. 1, Jan. 2019, pp. 358–72. Epmc, doi:10.1096/fj.201800534r.
Huynh NPT, Zhang B, Guilak F. High-depth transcriptomic profiling reveals the temporal gene signature of human mesenchymal stem cells during chondrogenesis. FASEB journal : official publication of the Federation of American Societies for Experimental Biology. 2019 Jan;33(1):358–372.

Published In

FASEB journal : official publication of the Federation of American Societies for Experimental Biology

DOI

EISSN

1530-6860

ISSN

0892-6638

Publication Date

January 2019

Volume

33

Issue

1

Start / End Page

358 / 372

Related Subject Headings

  • Tissue Engineering
  • Signal Transduction
  • Mesenchymal Stem Cells
  • Humans
  • High-Throughput Nucleotide Sequencing
  • Gene Regulatory Networks
  • Gene Expression Profiling
  • Chondrocytes
  • Cells, Cultured
  • Cell Differentiation