Low-energy shock wave pretreatment recruit circulating endothelial progenitor cells to attenuate renal ischaemia reperfusion injury

J Cell Mol Med. 2020 Sep;24(18):10589-10603. doi: 10.1111/jcmm.15678. Epub 2020 Aug 6.

Abstract

Low-energy shock wave (LESW) has been recognized as a promising non-invasive intervention to prevent the organs or tissues against ischaemia reperfusion injury (IRI), whereas its effect on kidney injury is rarely explored. To investigate the protective role of pretreatment with LESW on renal IRI in rats, animals were randomly divided into Sham, LESW, IRI and LESW + IRI groups. At 4, 12, 24 hours and 3 and 7 days after reperfusion, serum samples and renal tissues were harvested for performing the analysis of renal function, histopathology, immunohistochemistry, flow cytometry and Western blot, as well as enzyme-linked immunosorbent assay. Moreover, circulating endothelial progenitor cells (EPCs) were isolated, labelled with fluorescent dye and injected by tail vein. The fluorescent signals of EPCs were detected using fluorescence microscope and in vivo imaging system to track the distribution of injected circulating EPCs. Results showed that pretreatment with LESW could significantly reduce kidney injury biomarkers, tubular damage, and cell apoptosis, and promote cell proliferation and vascularization in IRI kidneys. The renoprotective role of LESW pretreatment would be attributed to the remarkably increased EPCs in the treated kidneys, part of which were recruited from circulation through SDF-1/CXCR7 pathway. In conclusion, pretreatment with LESW could increase the recruitment of circulating EPCs to attenuate and repair renal IRI.

Keywords: C-X-C chemokine receptor type 7; endothelial progenitor cells; ischaemia reperfusion injury; low-energy shock wave; stromal cell-derived factor 1.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis
  • Cell Movement
  • Chemokine CXCL12 / biosynthesis
  • Chemokine CXCL12 / genetics
  • Chemokine CXCL12 / physiology
  • Endothelial Progenitor Cells / physiology*
  • Extracorporeal Shockwave Therapy* / methods
  • Fluorescent Dyes / pharmacokinetics
  • In Situ Nick-End Labeling
  • Kidney / blood supply*
  • Kidney / pathology
  • Kidney / physiology
  • Male
  • Microscopy, Fluorescence
  • Microvessels / pathology
  • Random Allocation
  • Rats
  • Rats, Sprague-Dawley
  • Receptors, CXCR / antagonists & inhibitors
  • Receptors, CXCR / biosynthesis
  • Receptors, CXCR / genetics
  • Receptors, CXCR / physiology
  • Regeneration
  • Reperfusion Injury / blood
  • Reperfusion Injury / pathology
  • Reperfusion Injury / prevention & control*
  • Signal Transduction
  • Time Factors

Substances

  • Ackr3 protein, rat
  • CXCL12 protein, rat
  • Chemokine CXCL12
  • Fluorescent Dyes
  • Receptors, CXCR