Personal information

cardiac injury, regeneration, microRNA, extracellular vesicles, tissue engineering, targeting
Netherlands

Biography

In my research group, we focus on stimulating cardiac regeneration, thereby using approaches that can lead to improved recovery of cardiac tissue upon injury and improve the diagnosis of acute myocardial damage. In recent years, we identified miRNAs that can push cell lineage specifications and how we could improve progenitor cell transplantation, specifically improving local delivery and cell retentions. This was in close collaborations with Domian (Harvard), Sussman (San Diego State University), and Mercola (Sanford Burnham Medical Research Institute). My group substantially improved cell delivery to the myocardium, from which we also realized that most of the injected cell action was due to the potential paracrine actions. My group has therefore started to study the use of secreted exosomes by these cells as a novel approach to induce cardiac repair and aim to create a potential of-the-shelf therapy.
We have also identified several microRNAs that could be used as a direct therapeutic after myocardial damage has occured. Among them, miR-100 (Circulation 2011) and miR-214 for angiogenesis (CardioVascRes 2012), and miR-25 for heart failure (Nature 2014). These potent targets need smart delivery strategies to prevent side-effects; this directly lead me to initiate the BMM-LUST program that uses nano-medicine for targeted delivery. BMM-LUST made use of polymer-based delivery routes; the next leap in targeted delivery, I believe, lies in a natural carrier system. At this stage these polymer-based delivery routes are easily outperformed by the natural carrier system that transport biologicals between cells, called exosomes. I therefore propose the EVICARE program to combine my expertise in cardiac cell therapy, microRNA therapeutics and the use of our newly developed matrices for local delivery. My enthusiasm for introducing innovative molecular approaches and new therapeutic strategies, and my wide experiences in progenitor cell biology and preclinical animal model testing for cardiac injury will ensure that this research can go quickly from basic discoveries to preclinical testing in patient relevant animal models.

Activities

Employment (6)

University Medical Center Utrecht: Utrecht, Utrecht, NL

2017 to present | Professor of Cellar and translational Cardiology (Cardiology)
Employment
Source: Self-asserted source
Joost P.G. Sluijter

University Medical Center Utrecht: Utrecht, NL

2012 to 2017 | Associate Professor (Cardiology)
Employment
Source: Self-asserted source
Joost P.G. Sluijter

University Medical Center Utrecht: Utrecht, NL

2008 to 2012 | Assistant Professor (Cardiology)
Employment
Source: Self-asserted source
Joost P.G. Sluijter

University Medical Center Utrecht: Utrecht, NL

2005 to 2008 | Postdoctoral researcher (Cardiology)
Employment
Source: Self-asserted source
Joost P.G. Sluijter

Indiana University Purdue University at Indianapolis: Indianapolis, IN, US

2004 to 2005 | Postdoctoral researcher (Surgery)
Employment
Source: Self-asserted source
Joost P.G. Sluijter

Royal Netherlands Academy of Arts and Sciences: Utrecht, NL

2000 to 2004 | PhD (UMCU Utrecht)
Employment
Source: Self-asserted source
Joost P.G. Sluijter

Education and qualifications (1)

Utrecht University: Utrecht, NL

1995 to 2000 | BSc and MSc, Medical Biology
Education
Source: Self-asserted source
Joost P.G. Sluijter

Peer review (7 reviews for 5 publications/grants)

Review activity for ACS biomaterials science & engineering. (1)
Review activity for Advanced functional materials. (1)
Review activity for European heart journal. (2)
Review activity for Journal of cardiovascular translational research. (2)
Review activity for Trends in biotechnology. (1)