Methods of detection of mesenchymal stem cells in the kidneys during therapy of experimental renal pathologies

E Yu Plotnikov1, N V Pul'kova, D N Silachev

  • 1A. N. Belozerskii Institute of Physicochemical Biology, M. V. Lomonosov Moscow Medical University, Moscow, Russia.

Insights

Identifying mesenchymal multipotent stromal cells in kidney tissue was studied. Iron-labeled cell tracking via histology and immunohistochemistry proved most effective for observing cell migration in experimental kidney conditions.

Area of Science:

  • Regenerative Medicine
  • Cell Biology
  • Nephrology

Background:

  • Mesenchymal multipotent stromal cells (MSCs) hold therapeutic potential for kidney diseases.
  • Accurate identification and tracking of MSCs in renal tissue are crucial for evaluating treatment efficacy.
  • Experimental models of kidney injury, such as thermal ischemia and pyelonephritis, are essential for studying MSC behavior.

Purpose of the Study:

  • To compare different methods for identifying mesenchymal multipotent stromal cells (MSCs) within the renal parenchyma.
  • To evaluate the efficacy of in vivo and in vitro techniques, including magnetic resonance imaging (MRI) and immunological/immunohistochemical methods.
  • To determine the most informative approach for tracking MSCs in experimental kidney conditions.

Main Methods:

  • Comparison of in vivo and in vitro identification techniques for MSCs.
  • Utilized magnetic resonance imaging (MRI) for cell visualization.
  • Employed immunological and immunohistochemical methods for cell characterization.
  • Investigated labeling of stem cells with iron-containing particles for enhanced detection.
  • Performed histological identification and species-specific immunohistochemical staining.

Main Results:

  • Labeling MSCs with iron-containing particles followed by histological and immunohistochemical identification was the most informative method.
  • Demonstrated active migration of labeled MSCs to renal tissue.
  • Observed cell migration specifically in experimental acute pyelonephritis, correlating with inflammation foci.
  • Magnetic resonance imaging (MRI) and other immunological methods showed limitations in precise identification compared to the chosen approach.

Conclusions:

  • Iron-labeling combined with histological and immunohistochemical analysis provides a highly informative method for tracking mesenchymal multipotent stromal cells (MSCs) in renal parenchyma.
  • This approach successfully detected active MSC migration to sites of inflammation in experimental acute pyelonephritis.
  • The findings support the utility of advanced cell tracking techniques for understanding MSC behavior in kidney injury models.