Program Description:

Title: Therapeutic potential of endothelial progenitors
Speaker: Juan M. Melero-Martin
Description
Endothelial colony-forming cells (ECFCs) are endothelial precursors that circulate in peripheral blood and have enormous potential in regenerative medicine. This webinar will describe 1) what are ECFCs and how to isolate them from human blood; 2) how to effectively bioengineer vascular networks in vivo with human ECFCs; and 3) various potential therapeutic applications using ECFC-based vascular networks.
Title: Endothelial progenitors in the characterization of bleeding disorders
Speaker: Anna Randi
Description
Circulating endothelial progenitors can be expanded in vitro to differentiate into mature endothelial cells (EC), called endothelial colony-forming cells (ECFCs) or Blood outgrowth EC (BOEC). These cells allow for the first time to investigate cellular and molecular mechanisms underpinning diseases such as von Willebrand disease (VWD). This webinar will 1) summarise the current reports on ECFC/BOEC in patients with VWD ; 2) discuss their use in the characterization of the endothelial roles of VWF, with a focus on angiogenesis and angiodysplasia; 3) discuss the possible use of ECFC/BOEC in personalized medicine approaches.
Accreditation Statement
This activity has been planned and implemented in accordance with the accreditation requirements and policies of the Accreditation Council for Continuing Medical Education through the joint providership of The Medical College of Wisconsin and International Society on Thrombosis and Haemostasis. The Medical College of Wisconsin is accredited by the ACCME to provide continuing medical education for physicians.
Designation of Credit Statement:
The Medical College of Wisconsin designates this live activity for a maximum of 1.0 AMA PRA Category 1 Credit(s)™. Physicians should claim only the credit commensurate with the extent of their participation in the activity.
More information and online registration: http://academy.isth.org/
Target audience:
Clinicians and investigators with interest in:
- Vascular Biology
- Cardiovascular Diseases
- Bioengineering; Vascular Tissue Engineering
- Regenerative Medicine; Stem Cell Engraftment
- Von Willebrand Disease and congenital bleeding disorders
- Vascular roles of hemostatic proteins
- Regenerative Medicine; Personalized medicine
Learning objectives:
At the end of this Webinar, the participants will be able to:
- How to isolate and characterize human Endothelial Colony-Forming Cells (ECFCs).
- How to bioengineer a functional microvascular network using ECFCs.
- New insight into various potential therapeutic uses of ECFCs.
- What are the different cellular phenotypes of ECFC/BOEC in patients with VWD
- How these cells can be used to investigate endothelial function and angiogenesis
- Possible future applications of ECFC/BOEC in the treatment of angiodysplasia in VWD
Faculty & credentials:
Planning Committee:
Geoffrey Barnes, MD
Chris Ward, PhD
Stephen Watson, PhD
Speakers:
Juan Melero-Martin
Dr. Melero-Martin graduated in Chemical Engineering from University of Seville, Spain, in 1998. After working three years in industry, he went on to earn a PhD in Biochemical Engineering from the University of Birmingham, UK, in 2005. He then trained as a post-doctoral fellow in the Vascular Biology Program at Boston Children's Hospital. He joined the Department of Cardiac Surgery at Boston Children's Hospital and became Assistant Professor in Surgery, Harvard Medical School, in 2010.
Dr. Melero-Martin’s research is focused on how to build vascular networks and vascularize tissues. His laboratory is a reference in human blood-derived circulating endothelial colony-forming cells (ECFCs) and has contributed multiple original papers on various aspects of ECFC biology. His group has developed novel approaches to bioengineer vascular networks and has shown that bioengineered vascular networks can be generally used to harness the regenerative potential of other stem cells. In addition, his group developed a model that uses genetically-engineered ECFCs to achieve controlled release of therapeutic proteins in vivo.
You can read more about Dr. Melero-Martin’s research at meleromartinlab.com.
Anna Randi
Anna Randi is Professor of Cardiovascular Medicine at the National Heart and Lung Institute. Her main research interests are in vascular biology and vascular hemostasis. Prof. Randi is a clinically qualified haematologist, specialized in haemostasis and thrombosis. After graduation from the University of Milan (Italy), she obtained her PhD with Prof P.M. Mannucci, on the molecular basis of von Willebrand Disease. As part of her PhD studies, Prof. Randi spent 3 years at Washington University, in St. Louis (USA), in Dr. J.E. Sadler’s laboratory, where she was involved in the first characterization of mutations in the von Willebrand factor gene. Here Prof. Randi became interested in cell adhesion mechanisms and moved to the UK to study vascular inflammation at Cancer Research UK, in Dr. N. Hogg’s laboratory. Prof. Randi then established her research group in GlaxoSmithKline, where she eventually became Head of Translational Medicine in the Inflammation area. Whilst at GSK, Prof. Randi also held an honorary contract with Imperial College, and collaborated with Prof. D. Haskard and the British Heart Foundation on the genomics of cardiovascular diseases. She moved her lab to Imperial College in 2003.
Koralia Paschalaki
Dr. Paschalaki is a respiratory physician working as a Clinical Research Fellow in Professor Peter J. Barnes and Professor Anna Randi’s groups and in collaboration with Professor Athol Wells’ group (Interstitial Lung Disease Unit – Royal Brompton Hospital) at Imperial College London. She has developed a particular interest in the molecular mechanisms of endothelial dysfunction and vascular disease, since cardiovascular disease is the main cause of death in patients with chronic obstructive pulmonary disease (COPD), a chronic lung inflammatory disorder and the 3rd most frequent cause of death in the Western World. In her PhD study, she used circulating endothelial progenitors as a tool to study endothelial defects. She demonstrated that endothelial progenitors from smokers and COPD patients are senescent and dysfunctional and unable to correct vascular damage due to epigenetic alterations. This has been the first study that provides evidence of accelerated aging (senescence) of endothelial progenitors caused by cigarette smoke-oxidative stress, and is of great clinical importance as it may explain the link between COPD and cardiovascular disease. Her aim is to further investigate the pathways involved in endothelial dysfunction and vascular aging in chronic lung disorders and identify possible therapeutic targets for intervention. Understanding these mechanisms is important, as they highlight pathogenetic pathways involved in COPD and in other diseases, such as chronic kidney disease and diabetes mellitus, characterized by increased oxidative-stress and vascular dysfunction.
All persons in control of content have NO relevant financial relationships to disclose with the exception of the following persons:
Name | Company | Role |
| Geoffrey Barnes, MD | BMS/Pfizer, Blue Cross Blue Shield of MI, Aralez | Research Grant, Consulting |
| Chris Ward, PhD | Alexian, Bayer, Boehringer Ingelheim, Roche, Pfizer/BMS, Sanofi-aventis, CSL, Janssen, Amgen | Speaker, Advisory Board, Sponsored attendee, Speaker, Project Supervisor |
In accordance with the ACCME® Standards for Commercial Support Number 6, all in control of content disclosed any relevant financial relationships. These relationships were reviewed via the MCW conflict of interest resolution process and resolved
Contact
Session date:
04/26/2017 - 9:00am to 10:00am CDT
Location:
ISTH Webinar Library
Once a Month
Carrboro, NC
27510
United States
See map: Google Maps
Add to calendar:
- 1.00 AMA PRA Category 1 Credit(s)™AMA PRA Category 1 Credit(s)™
- 1.00 Hours of ParticipationHours of Participation credit.

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