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Differentiation; research in biological diversity2018; 105; 27-32; doi: 10.1016/j.diff.2018.12.002

Phospholipase A2 products predict the hematopoietic support capacity of horse serum.

Abstract: Horse serum is commonly used as an additive to support the maintenance of hematopoietic progenitor cells in culture. However, the wide variability in the performance of different lots calls for parallel testing of multiple batches over extended periods of culture. Identification of the serum components that determine hematopoietic support would therefore save considerable time and effort and would help to standardize culture procedures. We report here that the ability of horse serum to support the self-renewal of multipotent murine hematopoietic progenitor FDCP-Mix cells is correlated to the concentration of specific fatty acid products of phospholipase A2 and more closely to the spectrum of eicosanoids generated by their further processing through cyclooxygenase and lipoxygenase pathways. Supportive sera have low levels of lysophosphatidylcholine and inflammatory eicosanoids. This links known markers of inflammation, infection and platelet activation to the ability of serum to maintain progenitor cells in an undifferentiated state, providing a means for prospective identification of suitable sera as well as quality control of the production process.
Publication Date: 2018-12-06 PubMed ID: 30554008DOI: 10.1016/j.diff.2018.12.002Google Scholar: Lookup
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  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

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This research article investigates the factors that influence the effectiveness of horse serum in supporting the growth of hematopoietic progenitor cells. The scientists discover that specific byproducts of an enzyme known as phospholipase A2 are linked to the efficacy of the horse serum, and propose this as a standard for evaluating the quality of sera.

Main Findings of the Study

  • The study found that the horse serum’s capacity to support the growth of murine hematopoietic progenitor FDCP-Mix cells, which are cells that give rise to various types of blood cells, is associated with the concentration of specific fatty acid products produced by the enzyme phospholipase A2.
  • This correlation extended even further to the range of eicosanoids generated by further processing these products through two other enzymes, cyclooxygenase and lipoxygenase. Eicosanoids are signaling molecules made by the oxidation of 20-carbon fatty acids.
  • It was identified that sera capable of successful cell support had low levels of lysophosphatidylcholine and inflammatory eicosanoids.

Implications of the Study

  • This discovery connects established markers of inflammation, infection, and platelet activation to the horse serum’s ability to preserve progenitor cells in an undifferentiated state. This is a significant finding as it means these markers can potentially be utilized to predict the effectiveness of the serum in supporting cell growth.
  • Being able to prospectively identify suitable sera would streamline the process of maintaining these cells in culture as it would eliminate the need for extensive parallel testing of multiple batches over long periods.
  • Furthermore, this discovery provides a means of quality control for the horse serum production process, potentially making it more reliable and efficient.

Cite This Article

APA
Ditz T, Schnapka-Hille L, Noack N, Dorow J, Ceglarek U, Niederwieser D, Schiller J, Fuchs B, Cross M. (2018). Phospholipase A2 products predict the hematopoietic support capacity of horse serum. Differentiation, 105, 27-32. https://doi.org/10.1016/j.diff.2018.12.002

Publication

ISSN: 1432-0436
NlmUniqueID: 0401650
Country: England
Language: English
Volume: 105
Pages: 27-32
PII: S0301-4681(18)30101-4

Researcher Affiliations

Ditz, Timo
  • Institute of Medical Physics and Biophysics, Medical Faculty, University of Leipzig, Härtelstr. 16-18, D-04107 Leipzig, Germany; Department of Hematology and Oncology, Medical Faculty, University of Leipzig, Leipzig, Germany. Electronic address: timo.ditz@medizin.uni-leipzig.de.
Schnapka-Hille, Lydia
  • Department of Hematology and Oncology, Medical Faculty, University of Leipzig, Leipzig, Germany.
Noack, Nicole
  • Department of Hematology and Oncology, Medical Faculty, University of Leipzig, Leipzig, Germany.
Dorow, Juliane
  • Institute of Laboratory Medicine Clinical Chemistry and Molecular Diagnostics, University Hospital Leipzig, Leipzig, Germany.
Ceglarek, Uta
  • Institute of Laboratory Medicine Clinical Chemistry and Molecular Diagnostics, University Hospital Leipzig, Leipzig, Germany.
Niederwieser, Dietger
  • Department of Hematology and Oncology, Medical Faculty, University of Leipzig, Leipzig, Germany.
Schiller, Jürgen
  • Institute of Medical Physics and Biophysics, Medical Faculty, University of Leipzig, Härtelstr. 16-18, D-04107 Leipzig, Germany.
Fuchs, Beate
  • Institute of Medical Physics and Biophysics, Medical Faculty, University of Leipzig, Härtelstr. 16-18, D-04107 Leipzig, Germany; Leibniz-Institute for Farm Animal Biology (FBN), Wilhelm-Stahl-Allee 2, D-18196 Dummerstorf, Germany.
Cross, Michael
  • Department of Hematology and Oncology, Medical Faculty, University of Leipzig, Leipzig, Germany.

MeSH Terms

  • Animals
  • Eicosanoids / analysis
  • Eicosanoids / pharmacology
  • Hematopoiesis
  • Hematopoietic Stem Cells / cytology
  • Hematopoietic Stem Cells / drug effects
  • Horses
  • Lipids / analysis
  • Lipids / pharmacology
  • Lipoxygenase / metabolism
  • Lysophosphatidylcholines / analysis
  • Lysophosphatidylcholines / pharmacology
  • Mass Spectrometry
  • Mice
  • Phospholipases A2 / analysis
  • Phospholipases A2 / metabolism
  • Prostaglandin-Endoperoxide Synthases / metabolism
  • Serum / chemistry
  • Serum / metabolism

Citations

This article has been cited 3 times.
  1. Engel KM, Schiller J, Galuska CE, Fuchs B. Phospholipases and Reactive Oxygen Species Derived Lipid Biomarkers in Healthy and Diseased Humans and Animals - A Focus on Lysophosphatidylcholine.. Front Physiol 2021;12:732319.
    doi: 10.3389/fphys.2021.732319pubmed: 34858200google scholar: lookup
  2. Kosinska MK, Eichner G, Schmitz G, Liebisch G, Steinmeyer J. A comparative study on the lipidome of normal knee synovial fluid from humans and horses.. PLoS One 2021;16(4):e0250146.
    doi: 10.1371/journal.pone.0250146pubmed: 33861772google scholar: lookup
  3. Meth JL, Schoenfeld AR. Higher percentage of horse serum in culture media blocks attachment of PC12 cells.. Biotechniques 2019 Dec;67(6):256-258.
    doi: 10.2144/btn-2019-0073pubmed: 31621377google scholar: lookup