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Veterinary journal (London, England : 1997)2014; 202(3); 533-535; doi: 10.1016/j.tvjl.2014.08.026

Expression of putative markers of pluripotency in equine embryonic and adult tissues.

Abstract: Expression of several putative markers of pluripotency (OCT4, SOX2, NANOG, LIN28A, REX1, DNMT3B and TERT) was examined in a range of equine tissues, including early embryos, induced pluripotent stem cells (iPSCs), testis, adipose- and bone marrow-derived mesenchymal stromal cells (MSCs), and keratinocytes. Transcript levels of all markers were highest in embryos and iPSCs and, except for SOX2, were very low or undetectable in keratinocytes. Mean expression levels of all markers were lower in testis than in embryos or iPSCs and, except for DNMT3B, were higher in testis than in MSCs. Expression of OCT4, NANOG and DNMT3B, but not the other markers, was detected in MSCs. Of all markers analysed, only LIN28A, REX1 and TERT were associated exclusively with pluripotent cells in the horse.
Publication Date: 2014-08-29 PubMed ID: 25241949DOI: 10.1016/j.tvjl.2014.08.026Google Scholar: Lookup
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  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

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This study investigates the expression of several markers that potentially indicate pluripotency (the ability of a stem cell to develop into any cell type) in horse tissues including early embryos, induced pluripotent stem cells, testis, adipose- and bone marrow-derived mesenchymal stromal cells, and keratinocytes. The study confirmed that these markers show high expression in embryos and iPSCs and are largely absent in keratinocytes, highlighting hereto underexplored details of cell differentiation in horses.

Study Purpose and Methodology

  • The research aimed to identify and evaluate the expression of potential markers of pluripotency (OCT4, SOX2, NANOG, LIN28A, REX1, DNMT3B, and TERT) in various equine tissues. Pluripotency is the capacity of certain stem cells to differentiate into any type of cell in the human body.
  • To fulfil their objective, researchers examined these markers in early horse embryos, induced pluripotent stem cells (iPSCs), cells from the testes, adipose and bone marrow-derived mesenchymal stromal cells (MSCs), and keratinocytes (a type of skin cell).

Results and Key Findings

  • The results showed that transcripts (the first step of gene expression where part of the DNA is copied into RNA) for all markers were most abundant in horse embryos and iPSCs.
  • Except for the SOX2 marker, these transcripts were nearly absent or completely undetectable in keratinocytes. This suggests that keratinocytes have less pluripotent potential compared to embryos or iPSCs.
  • On average, all marker expression levels were lower in testis than in embryos or iPSCs.
  • With the exception of DNMT3B, marker expression levels were higher in testis than in MSCs. This suggests that the testis have a slightly higher potential for cell differentiation than MSCs.
  • The study found that only OCT4, NANOG and DNMT3B markers were present in MSCs. This indicates that certain levels of pluripotency exist within these types of cells.
  • Of all the markers studied, only LIN28A, REX1 and TERT were found exclusively in pluripotent cells in horses. This could suggest that these three markers are reliable indicators of pluripotency in horse cells.

Implications and Conclusion

  • The research provides valuable insight for future studies into pluripotency and cell differentiation in equines, especially with the potential therapeutic uses of such cells.
  • These results could have significant implications for regenerative medicine, tissue engineering, and other healthcare applications in veterinary practice.

Cite This Article

APA
Esteves CL, Sharma R, Dawson L, Taylor SE, Pearson G, Keen JA, McDonald K, Aurich C, Donadeu FX. (2014). Expression of putative markers of pluripotency in equine embryonic and adult tissues. Vet J, 202(3), 533-535. https://doi.org/10.1016/j.tvjl.2014.08.026

Publication

ISSN: 1532-2971
NlmUniqueID: 9706281
Country: England
Language: English
Volume: 202
Issue: 3
Pages: 533-535
PII: S1090-0233(14)00363-3

Researcher Affiliations

Esteves, Cristina L
  • The Roslin Institute and Royal (Dick) School of Veterinary Studies, University of Edinburgh, Easter Bush, Edinburgh EH25 9RG, Scotland, UK.
Sharma, Ruchi
  • The Roslin Institute and Royal (Dick) School of Veterinary Studies, University of Edinburgh, Easter Bush, Edinburgh EH25 9RG, Scotland, UK.
Dawson, Lucy
  • The Roslin Institute and Royal (Dick) School of Veterinary Studies, University of Edinburgh, Easter Bush, Edinburgh EH25 9RG, Scotland, UK.
Taylor, Sarah E
  • The Roslin Institute and Royal (Dick) School of Veterinary Studies, University of Edinburgh, Easter Bush, Edinburgh EH25 9RG, Scotland, UK.
Pearson, Gemma
  • The Roslin Institute and Royal (Dick) School of Veterinary Studies, University of Edinburgh, Easter Bush, Edinburgh EH25 9RG, Scotland, UK.
Keen, John A
  • The Roslin Institute and Royal (Dick) School of Veterinary Studies, University of Edinburgh, Easter Bush, Edinburgh EH25 9RG, Scotland, UK.
McDonald, Kieran
  • Biobest Laboratories, Edinburgh Technopole, Edinburgh EH26 0PY, UK.
Aurich, Christine
  • Artificial Insemination and Embryo Transfer, University of Veterinary Sciences, 1210 Vienna, Austria.
Donadeu, F Xavier
  • The Roslin Institute and Royal (Dick) School of Veterinary Studies, University of Edinburgh, Easter Bush, Edinburgh EH25 9RG, Scotland, UK. Electronic address: xavier.donadeu@roslin.ed.ac.uk.

MeSH Terms

  • Animals
  • Biomarkers / metabolism
  • Cell Differentiation
  • Embryo, Mammalian / embryology
  • Embryonic Development
  • Gene Expression Regulation, Developmental
  • Horses / embryology
  • Horses / genetics
  • Horses / metabolism
  • Induced Pluripotent Stem Cells / metabolism
  • Keratinocytes / metabolism
  • Male
  • Mesenchymal Stem Cells / metabolism
  • Organ Specificity
  • Testis / metabolism

Grant Funding

  • Biotechnology and Biological Sciences Research Council

Citations

This article has been cited 7 times.
  1. Trachsel DS, Stage HJ, Rausch S, Trappe S, Söllig K, Sponder G, Merle R, Aschenbach JR, Gehlen H. Comparison of Sources and Methods for the Isolation of Equine Adipose Tissue-Derived Stromal/Stem Cells and Preliminary Results on Their Reaction to Incubation with 5-Azacytidine.. Animals (Basel) 2022 Aug 11;12(16).
    doi: 10.3390/ani12162049pubmed: 36009640google scholar: lookup
  2. Scarlet D, Handschuh S, Reichart U, Podico G, Ellerbrock RE, Demyda-Peyrás S, Canisso IF, Walter I, Aurich C. Sexual Differentiation and Primordial Germ Cell Distribution in the Early Horse Fetus.. Animals (Basel) 2021 Aug 17;11(8).
    doi: 10.3390/ani11082422pubmed: 34438878google scholar: lookup
  3. Gastal GDA, Scarlet D, Melchert M, Ertl R, Aurich C. Epigenetic Changes in Equine Embryos after Short-Term Storage at Different Temperatures.. Animals (Basel) 2021 May 6;11(5).
    doi: 10.3390/ani11051325pubmed: 34066466google scholar: lookup
  4. Korody ML, Ford SM, Nguyen TD, Pivaroff CG, Valiente-Alandi I, Peterson SE, Ryder OA, Loring JF. Rewinding Extinction in the Northern White Rhinoceros: Genetically Diverse Induced Pluripotent Stem Cell Bank for Genetic Rescue.. Stem Cells Dev 2021 Feb;30(4):177-189.
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  5. Moro LN, Amin G, Furmento V, Waisman A, Garate X, Neiman G, La Greca A, Santín Velazque NL, Luzzani C, Sevlever GE, Vichera G, Miriuka SG. MicroRNA characterization in equine induced pluripotent stem cells.. PLoS One 2018;13(12):e0207074.
    doi: 10.1371/journal.pone.0207074pubmed: 30507934google scholar: lookup
  6. Olivera R, Moro LN, Jordan R, Pallarols N, Guglielminetti A, Luzzani C, Miriuka SG, Vichera G. Bone marrow mesenchymal stem cells as nuclear donors improve viability and health of cloned horses.. Stem Cells Cloning 2018;11:13-22.
    doi: 10.2147/SCCAA.S151763pubmed: 29497320google scholar: lookup
  7. Esteves CL, Sheldrake TA, Mesquita SP, Pesántez JJ, Menghini T, Dawson L, Péault B, Donadeu FX. Isolation and characterization of equine native MSC populations.. Stem Cell Res Ther 2017 Apr 18;8(1):80.
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