Accumulation of Multipotent Progenitor Cells on Polymethylpentene Membranes During Extracorporeal Membrane

Karla Lehle1, Lucas Friedl1, Julius Wilm1

  • 1Department of Cardiothoracic Surgery, University Medical Center, Regensburg, Germany.

Artificial Organs
|October 30, 2015
PubMed

Insights

Multipotent progenitor cells adhere to polymethylpentene (PMP) membrane oxygenator (MO) fibers during adult extracorporeal membrane oxygenation (ECMO). These cells differentiate into endothelial-like and mesenchymal-like cells, suggesting a role in ECMO device-related cellular processes.

Area of Science:

  • Biomedical Engineering
  • Cell Biology
  • Cardiovascular Research

Background:

  • Pediatric extracorporeal membrane oxygenation (ECMO) demonstrates mobilization of multipotent progenitor cells.
  • The behavior of these cells on polymethylpentene (PMP) fibers within membrane oxygenators (MOs) during adult ECMO is not well understood.

Purpose of the Study:

  • To investigate the adherence and characteristics of cells on PMP fibers within explanted adult ECMO membrane oxygenators.
  • To identify potential progenitor cell populations interacting with MOs during ECMO support.

Main Methods:

  • Mononuclear cells were isolated from explanted PMP-MOs (n=16).
  • Cells were cultured long-term, and outgrowth was analyzed via flow cytometry for surface markers.
  • Characterization included assessment of proliferative activity and functional assays like Dil-acetylated low-density lipoprotein uptake.

Main Results:

  • Spindle-shaped cells initially attached but lacked proliferation.
  • Long-term cultures yielded proliferative leukocytoid, endothelial-like, and mesenchymal-like cells.
  • Endothelial-like cells formed capillary structures and exhibited LDL uptake; both endothelial- and mesenchymal-like cells adhered to PMP-MO surfaces.

Conclusions:

  • Adult ECMO support involves the adherence of progenitor cells to PMP-MO fibers.
  • These cells can differentiate into distinct populations with varying surface markers and functional capacities.
  • Further investigation is required to determine the clinical significance of these cellular interactions within ECMO devices.

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