Immunofluorescence Protocol for Characterization of Platelet and Leukocyte Binding in Extracorporeal Membrane Oxygenation (ECMO) Circuits

Author:

Cai Tengyi12ORCID,Burton Matthew3,McCafferty Conor12,Van Den Helm Suelyn12,Letunica Natasha1,Attard Chantal12,Horton Stephen24,Bottrell Steve4,Schultz Bradley4,MacLaren Graeme5,Chiletti Roberto67,Best Derek67,Johansen Amy67,Newall Fiona127,Butt Warwick267,d’Udekem Yves8,Monagle Paul1279,Ignjatovic Vera1245

Affiliation:

1. the Haematology Research, Murdoch Children’s Research Institute, Parkville, Australia

2. Department of Paediatrics, The University of Melbourne, Parkville, Australia

3. Flow Cytometry and Imaging, Murdoch Children’s Research Institute, Parkville, Australia

4. Cardiac Surgery, The Royal Children’s Hospital, Parkville, Australia

5. Cardiothoracic Intensive Care Unit, National University Health System, Singapore

6. Intensive Care, The Royal Children’s Hospital, Parkville, Australia

7. Paediatric Intensive Care Research Group, Murdoch Children’s Research Institute, Parkville, Australia

8. Clinical Haematology, The Royal Children’s Hospital, Parkville, Australia

9. Cardiovascular Surgery, Children’s National Heart Institute, Washington, DC

Abstract

The continuous contact between blood and the foreign surface of the extracorporeal membrane oxygenation (ECMO) circuit contributes to hemostatic, inflammatory, and other physiological disturbances observed during ECMO. Although previous studies have extensively investigated blood samples from patients on ECMO, cell adsorption to the ECMO circuit as an additional factor that could potentially influence clinical outcomes, has largely been overlooked. Here we provide a detailed immunofluorescence (IF) protocol designed to characterize cellular binding on ECMO circuits collected from patients. Extracorporeal membrane oxygenation circuits were collected from three pediatric patients and an albumin primed-only ECMO circuit was used as control. Circuit samples from five different sites within each ECMO circuit were collected and processed for the IF protocol. CD14 and CD42a antibodies were used to identify platelets and leukocytes bound to each ECMO circuit sample and images captured using inverted fluorescence microscopy. The protocol enables the comprehensive characterization of platelet and leukocyte binding to ECMO circuits collected from patients, which could in turn extend our knowledge of the characteristics of circuit binding and may provide guidance for improved ECMO circuit design.

Publisher

Ovid Technologies (Wolters Kluwer Health)

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