Summary

Exosome Isolation after in vitro Shock Wave Therapy

Published: September 10, 2020
doi:

Summary

Exosomes are released upon in vitro application of shockwaves. Here, we describe how to apply shockwaves on cultured endothelial cells and subsequently isolate exosomes for further investigation.

Abstract

Shock wave therapy is routinely applied in orthopedic indications including tendinopathies such as lateral epicondylitis (tennis elbow) and Achilles tendinitis (heel spurs) as well as non-healing wounds and bones. Despite different pathologies, the combination of an angiogenic and an anti-inflammatory effect of shock wave therapy leads to regeneration in soft tissue and bones. In over 30 years of clinical application, no side effects were observed. Furthermore, basic research even revealed regenerative effects on ischemic myocardium.

In a previous work we could show that the mechanical stimulus of cultured cells is translated via an exosome release into a biological response. However, the exact mechanism remains to be elucidated. Mechanical coupling is crucial when applying shock wave therapy as even small air bubbles can absorb shock waves. The previously described water bath method is a valid method to guarantee adequate and reproducible shock wave application in vitro.

We were able to develop a feasible and replicable protocol to isolate exosomes from cultured cells after shock wave application. Thereby we demonstrate a possibility to study underlying mechanisms of mechanotransduction as well as the regenerative and angiogenic potential of shock wave released exosomes.

Introduction

Shock waves (SW) are sound pressure waves that appear in nature when a high amount of energy is released in a short period of time (e.g., thunder with lightning). In clinical routine, shock waves are used in lithotripsy to disintegrate kidney stones without relevant side effects for over 30 years1,2. By incident, a thickening of the iliac bone was observed in X-rays after kidney stone disintegration. This observation provided the basis for research in bone healing disorders and lead to treatment in long-bone non unions3,4,5.

Indications for shock wave therapy were expanded and today the method is in routine clinical use in orthopedic indications including tendinopathies such as lateral epicondylitis (tennis elbow) and Achilles tendinitis (heel spurs)6,7. Furthermore, basic research demonstrated a high angiogenic potential of shock wave therapy (SWT). Therein, a study showed an increase in angiogenic growth factors such as VEGF (vascular endothelial growth factor), PIGF (placental growth factor) and FGF (vascular endothelial growth factor) upon SWT followed by angiogenesis8.

To investigate a possible beneficial role of shock wave induced angiogenesis in other pathologies, we applied SW therapy in an animal model of ischemic heart disease9,10. After a regenerative effect in the ischemic myocardium could be demonstrated, we could identify the indispensable role of the innate immune receptor TLR 3 (Toll like receptor 3) upon shock wave therapy11,12. Further studies showed that the mechanical stimulus of SW therapy is translated into a biological signal via exosome release. Compared to exosomes physiologically released from endothelial cells, exosomes released upon SWT contain an increased cargo of angiogenic microRNA. Injected into ischemic myocardium, SWT released exosomes induced regeneration13.

Since air absorbs SW, perfect coupling between the applicator and the cell culture flasks is crucial. A standardized water bath represents a feasible method to apply SWT in vitro and a reproducible experimental setup. In order to avoid a reflection and consequently interference of waves, a wedge-shaped absorber destructs the primary waves running to the back of the water bath. For this reason, we recommend applying shock waves in vitro using the described water bath only.

In this protocol we describe the application of shock waves in vitro to release angiogenic exosomes into the supernatant. This protocol provides the possibility to investigate the role of exosomes in mechanotransduction and is the basis for further investigation of exosome release upon SWT.

Protocol

Human umbilical vein endothelial cells were obtained from caesarean sections at the Department of Gynecology. Therefore, written informed consent of patients was obtained. Permission was given from the ethics committee of Innsbruck Medical University (no. UN4435). NOTE: Work under a sterile laminar flow hood to avoid contamination. 1. 24 h before the experiment Prepare exosome free endothelial growth medium by ultra-centrifuging fetal bovine serum (FCS) …

Representative Results

Using the described protocol, we subjected human endothelial cells (HUVECs) as well as human coronary artery endothelial cells (CAECs; PromoCell) to shock wave therapy (e.g., Orthowave 180c). Released vesicles were quantified via nano tracking analysis (NTA). Thereby, we could observe an increase in microvesicle release upon SW therapy (Figure 1A,B). Imaging of HUVECs released vesicles via transmission electron microscopy revealed the characteristic 100 nm size of the exosom…

Discussion

In multiple basic research works, the regenerative effect of the shock wave therapy could be demonstrated and is routinely applied in orthopedic indications3,4,5. In diverse animal models, the regenerative effect on the ischemic myocardium could be demonstrated and lead to the initiation of the CAST-HF trial9,10. This randomized controlled trial aims to evaluate the bene…

Disclosures

The authors have nothing to disclose.

Acknowledgements

This study was supported by an unrestricted AUVA research grant to JH and CGT.

Materials

Cell culture flasks  Cellstar  658170 75 cm2
Collection tubes – Falcon Tube Corning  352070
Endothelial Cell Growth Medium-2 BulletKit  Lonza  CC-3162
Endothelial Cell Growth Basal Medium  Lonza CC-3121
Fetal bovine serum  Sigma  F0804
Parafilm  Pechiney  PM996
Phosphat buffered saline gibco  14190-904
Shockwave applicator MTS Orthowave 180c

References

  1. Pearle, M. S., et al. Shock-wave lithotripsy for renal calculi. The New England Journal of Medicine. 367 (1), 50-57 (2012).
  2. Chaussy, C., Brendel, W., Schmiedt, E. Extracorporeally Induced Destruction of Kidney Stones By Shock Waves. Lancet. 316 (8207), 1265-1268 (1980).
  3. Valchanou, V. D., Michailov, P. High energy shock waves in the treatment of delayed and nonunion of fractures. International Orthopedics. 15 (3), 181-184 (1991).
  4. Haupt, G., Haupt, A., Ekkernkamp, A., Gerety, B., Chvapil, M. Influence of shock waves on fracture healing. Urology. 39 (6), 529-532 (1992).
  5. Moretti, B., et al. Bone healing induced by ESWT. Clinical Cases in Mineral and Bone Metabolism. 6 (2), 155-158 (2009).
  6. Romeo, P., Lavanga, V., Pagani, D., Sansone, V. Extracorporeal shock wave therapy in musculoskeletal disorders: A review. Medical Principles and Practice. 23 (1), 7-13 (2014).
  7. Schaden, W., et al. Shock Wave Therapy for Acute and Chronic Soft Tissue Wounds: A Feasibility Study. Journal of Surgical Research. 143 (1), 1-12 (2007).
  8. Holfeld, J., et al. Low energy shock wave therapy induces angiogenesis in acute hind-limb ischemia via VEGF receptor 2 phosphorylation. PLoS One. 9 (8), 1-7 (2014).
  9. Zimpfer, D., et al. Direct epicardial shock wave therapy improves ventricular function and induces angiogenesis in ischemic heart failure. Journal of Thoracic and Cardiovascular Surgery. 137 (4), 963-970 (2009).
  10. Holfeld, J., et al. Epicardial shock-wave therapy improves ventricular function in a porcine model of ischemic heart disease. Journal of Tissue Engineering and Regenerative Medicine. 10, 1057-1064 (2016).
  11. Holfeld, J., et al. Toll-like receptor 3 signaling mediates angiogenic response upon shock wave treatment of ischemic muscle. Cardiovascular Research. 109 (2), 331-343 (2016).
  12. Tepeköylü, C., et al. Shockwaves prevent from heart failure after acute myocardial ischemia via RNA/protein complexes. Journal of Cellular and Molecular Medicine. 21 (4), 791-801 (2017).
  13. Gollmann-Tepeköylü, C., et al. miR-19a-3p containing exosomes improve function of ischemic myocardium upon shock wave therapy. Cardiovascular Research. , (2019).
  14. Pölzl, L., et al. Safety and efficacy of direct Cardiac Shockwave Therapy in patients with ischemic cardiomyopathy undergoing coronary artery bypass grafting (the CAST-HF trial), Study protocol for a randomized controlled trial. Trials. 21 (1), 1-10 (2020).
  15. Holfeld, J., et al. Shock wave application to cell cultures. Journal of Visualized Experiments. (86), e51076 (2014).
This article has been published
Video Coming Soon
Keep me updated:

.

Cite This Article
Pölzl, L., Nägele, F., Hirsch, J., Graber, M., Grimm, M., Gollmann-Tepeköylü, C., Holfeld, J. Exosome Isolation after in vitro Shock Wave Therapy. J. Vis. Exp. (163), e61508, doi:10.3791/61508 (2020).

View Video