Heparin Differentially Regulates the Expression of Specific miRNAs in Mesenchymal Stromal Cells

Michaela Oeller (First author), Tanja Schally (Co-author), Georg Zimmermann (Co-author), Wanda Lauth (Co-author), Katharina Schallmoser (Co-author), Eva Rohde (Co-author), Sandra Laner-Plamberger* (Last author)

*Corresponding author for this work

Research output: Contribution to journalOriginal Articlepeer-review

Abstract

In regenerative medicine, stromal cells are supposed to play an important role by modulating immune responses and differentiating into various tissue types. The aim of this study was to investigate the influence of heparin, frequently used as an anticoagulant in human platelet lysate (HPL)-supplemented cell cultures, on the expression of non-coding RNA species, particularly microRNAs (miRNA), which are pivotal regulators of gene expression. Through genomic analysis and quantitative RT-PCR, we assessed the differential impact of heparin on miRNA expression in various stromal cell types, derived from human bone marrow, umbilical cord and white adipose tissue. Our results demonstrate that heparin significantly alters miRNA expression, with distinct up- and downregulation patterns depending on the original tissue source of human stromal cells. Furthermore, our analyses indicate that these heparin-induced alterations in miRNA expression profiles influence critical cellular processes, including proliferation, apoptosis and differentiation. In conclusion, our study highlights that heparin not only fulfills its primary role as an efficient anticoagulant but can also modulate important regulatory pathways in stromal cells by influencing miRNA expression. This may alter cellular properties and thus influence stromal cell-based therapeutic applications in regenerative medicine.
Original languageEnglish
Article number12589
Number of pages14
JournalINTERNATIONAL JOURNAL OF MOLECULAR SCIENCES
Volume25
Issue number23
DOIs
Publication statusPublished - Dec 2024

Keywords

  • MSCs
  • Expression
  • Heparin
  • Human platelet lysate
  • miRNAs
  • non-coding RNAs
  • Stromal cells

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