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Related Concept Videos

Mesenchymal Stem Cells01:19

Mesenchymal Stem Cells

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Mesenchymal stem cells (MSCs) are adult stem cells that can differentiate into most connective tissue cell types, except for hematopoietic cells, depending upon the source of MSCs. For example, bone-marrow-derived MSCs (BM-MSCs) can differentiate into osteocytes, hepatocytes, and pancreatic and neuronal cells. MSCs can be isolated from various sources such as bone marrow, placenta, adipose tissue, teeth, and Wharton’s jelly, a gelatinous substance in the umbilical cord. The ease of their...
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lncRNA - Long Non-coding RNAs02:39

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In humans, more than 80% of the genome gets transcribed. However, only around 2% of the genome codes for proteins. The remaining part produces non-coding RNAs which includes ribosomal RNAs, transfer RNAs, telomerase RNAs, and regulatory RNAs, among other types. A large number of regulatory non-coding RNAs have been classified into two groups depending upon their length – small non-coding RNAs, such as microRNA, which are less than 200 nucleotides in length, and long non-coding RNA...
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Isolating, Sequencing and Analyzing Extracellular MicroRNAs from Human Mesenchymal Stem Cells
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Long non-coding RNA exploration for mesenchymal stem cell characterisation.

Sébastien Riquier1, Marc Mathieu1, Chloé Bessiere1

  • 1IRMB, University of Montpellier, INSERM, 80 rue Augustin Fliche, Montpellier, France.

BMC Genomics
|June 5, 2021
PubMed
Summary
This summary is machine-generated.

Researchers identified novel long non-coding RNAs (lncRNAs) as potential biomarkers for Mesenchymal Stem Cells (MSCs). This discovery offers new tools for understanding MSC biology and clinical applications.

Keywords:
BioinformaticsLong non-coding RNAMesenchymal stem cellNGS analysisRNAseqTranscriptomics

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Area of Science:

  • Transcriptomics
  • Stem Cell Biology
  • Bioinformatics

Background:

  • RNA sequencing (RNAseq) enables new approaches for identifying transcriptional markers.
  • Long non-coding RNAs (lncRNAs) show potential for tissue-specific functions.
  • Mesenchymal Stem Cells (MSCs) are clinically relevant but lack extensive characterization.

Purpose of the Study:

  • To explore the biomarker potential of lncRNAs in Mesenchymal Stem Cells (MSCs).
  • To develop a method for identifying cell-specific unannotated lncRNAs.

Main Methods:

  • Developed a bioinformatics pipeline for ab initio transcript identification and expression quantification.
  • Utilized a k-mer approach for naive quantification of lncRNA expression from RNAseq data.
  • Applied functional prediction methods to assess the role of identified lncRNAs.

Main Results:

  • Identified novel lncRNAs with high specificity in MSCs.
  • Demonstrated that candidate lncRNAs represent specific states of MSC biology.
  • Highlighted potential lncRNA actors involved in MSC functions.

Conclusions:

  • The developed approach effectively harnesses lncRNAs as cell-specific markers.
  • Identified lncRNAs offer promising candidates for future experimental validation in MSC biology.