Stem cell therapies for heart disease – one step closer
Press release issued: 30 October 2008
New research from the University of Bristol brings stem cell therapies for heart disease one step closer.
Dr Nicolle Kränkel and colleagues at the Bristol Heart Institute have discovered how our bodies initiate DIY rescue and repair mechanisms when blood supply is inadequate, for example in diabetic limbs or in the heart muscle during heart attack. Their findings also provide a practical step to advance progress in stem cell therapies.
In healthy people, reduced oxygen supply can occur in certain situations, e.g. after an injury. The affected tissues release chemical messengers that ‘call’ to a type of circulating stem cells (EPCs) for help to re-establish blood supply via the growth of new blood vessels. A group of Bristol researchers have found that kinins, for long time considered inflammatory substances, are among the messengers supporting blood vessel growth.
In this study, published in Circulation Research, Dr Kränkel and colleagues found that EPCs respond to kinins by travelling to the target tissue and invading it to assist healing. In patients with angina, EPCs cannot respond to the distress call because they lack a kinin sensor (the ‘kinin receptor’) on their surface. The oxygen-starved tissue is therefore left with reduced blood supply.
In heart attack patients they saw that a proportion of the circulating EPCs were able to sense the kinin signal and respond.
Dr Nicolle Kränkel , Research Associate at the Bristol Heart Institute, said: “Our findings showed that heart attack patients possess the functional cells needed to repair blood supply to their heart, but they’re hidden amongst a muddle of others.”
The team purified the kinin-sensitive EPCs from the total stem cell population to create an enriched sample that has huge potential as a powerful regenerative therapy.
Dr Kränkel added: “In previous clinical stem cell trials, a mixture of different types of cells were used. We’ve used kinin like a magnet to attract and extract the most effective repair cells from the mass of different types. This enriched sample should increase the therapeutic potential, especially in heart attack patients where quick and efficient treatment is crucial for long term outcome.”
Professor Jeremy Pearson, Associate Medical Director of the British Heart Foundation – one of the study’s funders – said: “The team have made fascinating discoveries about our DIY repair systems and have translated them into practical use. They’ve intelligently employed the body’s own strategies to develop a method that may take us a step closer to truly effective stem cell therapies for heart patients.”
Dr Kränkel is a research fellow in the laboratory of Paolo Madeddu, Professor of Experimental Cardiovascluar Medicine at the Bristol Heart Institute, Bristol Royal Infirmary. The study was funded by grants from the British Heart Foundation, European Foundation for the Study of Diabetes, Juvenile Diabetes Research Foundation and Novo Nordisk.
Further informationPaper: Role of Kinin B2 Receptor Signaling in the Recruitment of Circulating Progenitor Cells With Neovascularization Potential
Authors: Nicolle Kränkel, Rajesh G. Katare, Mauro Siragusa, Luciola S. Barcelos, Paola Campagnolo, Giuseppe Mangialardi, Orazio Fortunato, Gaia Spinetti, Nguyen Tran, Kai Zacharowski, Wojciech Wojakowski, Iwona Mroz, Andrew Herman, Jocelyn E. Manning Fox, Patrick E. MacDonald, Joost P. Schanstra, Jean Loup Bascands, Raimondo Ascione, Gianni Angelini, Costanza Emanueli and Paolo Madeddu
Published online in Circulation Research, Oct 16, 2008.
The Bristol Heart Institute consists of over 200 researchers and clinicians in the University of Bristol and Bristol NHS Trusts. As well as improving collaboration between scientists and clinicians within the Institute, the aim is to communicate research findings to the public.
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