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Journal of equine science2016; 27(2); 57-65; doi: 10.1294/jes.27.57

Characteristics and multipotency of equine dedifferentiated fat cells.

Abstract: Dedifferentiated fat (DFAT) cells have been shown to be multipotent, similar to mesenchymal stem cells (MSCs). In this study, we aimed to establish and characterize equine DFAT cells. Equine adipocytes were ceiling cultured, and then dedifferentiated into DFAT cells by the seventh day of culture. The number of DFAT cells was increased to over 10 million by the fourth passage. Flow cytometry of DFAT cells showed that the cells were strongly positive for CD44, CD90, and major histocompatibility complex (MHC) class I; moderately positive for CD11a/18, CD105, and MHC class II; and negative for CD34 and CD45. Moreover, DFAT cells were positive for the expression of sex determining region Y-box 2 as a marker of multipotency. Finally, we found that DFAT cells could differentiate into osteogenic, chondrogenic, and adipogenic lineages under specific nutrient conditions. Thus, DFAT cells could have clinical applications in tissue regeneration, similar to MSCs derived from adipose tissue.
Publication Date: 2016-06-21 PubMed ID: 27330399PubMed Central: PMC4914398DOI: 10.1294/jes.27.57Google Scholar: Lookup
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  • Journal Article

Summary

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The research paper presents the characteristics of equine Dedifferentiated Fat (DFAT) cells and their ability to differentiate into various cells, similar to mesenchymal stem cells (MSCs). The paper highlights the potential clinical applications of DFAT cells in tissue regeneration.

Objective and Procedure

  • The goal of the research was to establish and examine the characteristics of equine DFAT cells, exploring their multipotency, which is their ability to differentiate into different cell types.
  • To achieve this, the researchers conducted a ceiling culture of equine adipocytes – the fat cells, allowing them to dedifferentiate into DFAT cells by the seventh day of the culture.
  • They continued by magnifying cell growth, with over 10 million DFAT cells produced by the fourth passage.

Findings

  • Flow cytometry was used to measure the physical and chemical characteristics of the DFAT cells.
  • Researchers observed that the DFAT cells were strongly positive to CD44, CD90 and major histocompatibility complex (MHC) class I. This suggests that the cells have the ability to interact with the immune system.
  • These cells were also moderately positive to CD11a/18, CD105, and MHC class II, while being negative for CD34 and CD45. This indicates that the cells have no hematopoietic (blood forming) potential.
  • Importantly, the DFAT cells were found to express Sex determining region Y-box 2 (SOX2), which is a marker for multipotency or the ability to form multiple cell types.

Differentiation Potential

  • The researchers tested the differentiation ability of DFAT cells.
  • They reported that under specific nutrient conditions, the DFAT cells could differentiate into osteogenic, chondrogenic, and adipogenic lineage. This implies that these cells could change into bone, cartilage and fat cells respectively.

Conclusions and Implications

  • The study shows that equine DFAT cells, like Mesenchymal Stem Cells derived from adipose tissue, have the ability to differentiate into different kinds of cells.
  • Thus, they are suggested to have potential clinical applications in tissue regeneration, through their multipotency.

Cite This Article

APA
Murata D, Yamasaki A, Matsuzaki S, Sunaga T, Fujiki M, Tokunaga S, Misumi K. (2016). Characteristics and multipotency of equine dedifferentiated fat cells. J Equine Sci, 27(2), 57-65. https://doi.org/10.1294/jes.27.57

Publication

ISSN: 1340-3516
NlmUniqueID: 9503751
Country: Japan
Language: English
Volume: 27
Issue: 2
Pages: 57-65

Researcher Affiliations

Murata, Daiki
  • Department of Veterinary Clinical Science, Joint Faculty of Veterinary Medicine, Kagoshima University, Kagoshima 890-0065, Japan.
Yamasaki, Atsushi
  • Department of Veterinary Clinical Science, Joint Faculty of Veterinary Medicine, Kagoshima University, Kagoshima 890-0065, Japan.
Matsuzaki, Shouta
  • Department of Veterinary Clinical Science, Joint Faculty of Veterinary Medicine, Kagoshima University, Kagoshima 890-0065, Japan.
Sunaga, Takafumi
  • Department of Veterinary Clinical Science, Joint Faculty of Veterinary Medicine, Kagoshima University, Kagoshima 890-0065, Japan.
Fujiki, Makoto
  • Department of Veterinary Clinical Science, Joint Faculty of Veterinary Medicine, Kagoshima University, Kagoshima 890-0065, Japan.
Tokunaga, Satoshi
  • Department of Veterinary Clinical Science, Joint Faculty of Veterinary Medicine, Kagoshima University, Kagoshima 890-0065, Japan.
Misumi, Kazuhiro
  • Department of Veterinary Clinical Science, Joint Faculty of Veterinary Medicine, Kagoshima University, Kagoshima 890-0065, Japan.

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Citations

This article has been cited 5 times.
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