4.7 Article

Stem cell delivery to kidney via minimally invasive ultrasound-guided renal artery injection in mice

Journal

SCIENTIFIC REPORTS
Volume 10, Issue 1, Pages -

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/s41598-020-64417-2

Keywords

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Funding

  1. EPSRC [EP/L006472/1]
  2. MRC via the UK Regenerative Medicine Platform Safety and Efficacy Hub [MR/K026739/1]
  3. British Heart Foundation intermediate basic science research fellowship [FS/15/33/31608]
  4. BHF Centre for Regenerative Medicine [RM/17/1/33377]
  5. Wellcome Trust multi users equipment grant [212937/Z/18/Z]
  6. MRC [MR/R026416/1]
  7. National Institute for Health Research University College London Hospitals Biomedical Research Centre
  8. Wellcome Trust [212937/Z/18/Z] Funding Source: Wellcome Trust
  9. EPSRC [EP/L006472/1] Funding Source: UKRI
  10. MRC [MR/R026416/1] Funding Source: UKRI

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Cell-based therapies are promising treatments for various kidney diseases. However, the major hurdle in initiating therapeutic responses is the inefficiency of injection routes to deliver cells to the kidney parenchyma. Systemic injection, such as intravenous injection only delivers a small proportion of cells to the kidney. Whereas direct delivery, such as renal artery injection requires surgical procedures. A minimally invasive renal artery injection was therefore developed to enhance cell delivery to kidney. In this study, luciferase expressing human adipocyte derived stem cells (ADSC) were labelled with gold nanorods (GNR) and injected into the renal artery using ultrasound guidance. The ADSCs were tracked using bioluminescence and photoacoustic imaging serially over 7 days. Imaging confirmed that the majority of signal was within the kidney, indicative of successful injection and that the cells remained viable for 3 days. Histology showed co-localization of GNRs with ADSC staining throughout the kidney with no indication of injury caused by injection. These findings demonstrate that ultrasound-guided renal artery injection is feasible in mice and can successfully deliver a large proportion of cells which are retained within the kidney for 3 days. Therefore, the techniques developed here will be useful for optimising cell therapy in kidney diseases.

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