idw – Informationsdienst Wissenschaft

Nachrichten, Termine, Experten

Grafik: idw-Logo
Thema Corona

Imagefilm
Science Video Project
idw-News App:

AppStore



Share on: 
11/05/2020 09:00

Graz researchers identify biomarker for cardiovascular diseases

Mag. Christoph Pelzl, MSc Kommunikation und Marketing
Technische Universität Graz

    The role of the enzyme dipeptidyl peptidase 3 in the blood pressure-regulating renin-angiotensin system was investigated in the inter-university cooperation project BioTechMed-Graz. The results could pave the way for new therapies for cardio-renal diseases.

    The renin-angiotensin system (RAS) becomes active at low blood pressure and forms angiotensin II, a hormone that causes blood vessels to constrict, causing blood pressure to rise again. The enzyme dipeptidyl peptidase 3 (DPP3) is significantly involved in the metabolism of angiotensin II.

    The head of the Institute of Biochemistry at Graz University of Technology, Peter Macheroux, and his team are world leaders in DPP3 research: "For example, we now know that people who suffer a heart attack, blood poisoning or acute kidney injury have elevated levels of DPP3 in their bloodstream. This increase correlates with increased mortality." However, little is known about the physiological function of DPP3. For this reason, the working group led by Macheroux, together with researchers from the University of Graz and Med Uni Graz, investigated how DPP3 affects the RAS. The results were published in the Journal of Biological Chemistry.

    Effects of DPP3 deficiency

    The DPP3 gene was specifically switched off in a mouse model at the University of Graz (knock-out mouse model). Using mass spectroscopic analyses, the researchers discovered that DPP3 regulates RAS processes and the water balance by breaking down angiotensin peptides. The DPP3 deficiency led to increased fluid and food intake. Nevertheless, the knock-out mice had a lower body weight and less fat mass than the mice of the control group (wild type mice). Furthermore, the concentration of angiotensin II was significantly higher in knock-out mice. This increased angiotensin II level caused oxidative stress and reduced metabolism. "The exact effects of these changes are still unclear, however, and will have to be examined in more detail in follow-up studies. For example, the blood pressure did not change measurably," said Macheroux.

    Gender-specific differences

    For the first time it was also possible to prove that there are gender-specific differences. While major changes in RAS were found in male mice, female mice were hardly affected by DPP3 knock-out. "This documents a direct connection between the hormone system and the physiological role of DPP3. Oestrogen in particular is likely to inhibit the production of angiotensin II," say the two first authors Shalinee Jha and Ulrike Taschler from the Institute of Biochemistry at TU Graz and the Institute of Molecular Biosciences at the University of Graz.

    Development of an inhibitor

    The characterization of DPP3 in this study shows that DPP3 can modulate metabolic and cellular processes in RAS. This property could be of great benefit in the treatment of various cardiovascular diseases in the future. Macheroux: "In a next step, we would like to advance the development of an enzyme-inhibiting substance (inhibitor) for DPP3. Work on this has already begun at the Institutes of Biochemistry and Organic Chemistry at TU Graz."

    This research is anchored in the Field of Expertise "Human & Biotechnology", one of five strategic focal areas of Graz University of Technology.
    The study was carried out within the framework of the BioTechMed-Graz initiative, a cooperation project between the University of Graz, the Medical University of Graz and Graz University of Technology involving cooperation and networking at the interface of biomedical basics, technological developments and medical applications with the aim of joint research in health. For more information, see https://biotechmedgraz.at


    Contact for scientific information:

    Contact at TU Graz:
    Peter MACHEROUX
    Univ.-Prof. Dr.rer.nat.
    TU Graz | Institute of Biochemistry
    Phone: +43 316 873 6450
    peter.macheroux@tugraz.at

    Contact at the University of Graz:
    Robert ZIMMERMANN
    Assoz. Prof. Mag. Dr.rer.nat.
    University of Graz | Institute of Molecular Biosciences
    Phone: +43 316 380 1914
    robert.zimmermann@uni-graz.at


    Original publication:

    Dipeptidyl peptidase 3 modulates the renin-angiotensin system in mice
    Shalinee Jha, Ulrike Taschler, Oliver Domenig, Marko Poglitsch, Benjamin Bourgeois, Marion Pollheimer, Lisa M. Pusch, Grazia Malovan, Sasa Frank, Tobias Madl, Karl Gruber, Robert Zimmermann and Peter Macheroux
    J. Biol. Chem. 2020, 295:13711-13723.
    DOI: 10.1074/jbc.RA120.014183


    Criteria of this press release:
    Journalists, Scientists and scholars
    Biology, Chemistry, Medicine
    transregional, national
    Scientific Publications
    English


    In a paper published in the Journal of Biological Chemistry, BioTechMed-Graz researchers Robert Zimmermann, Ulrike Taschler, Peter Macheroux, Shalinee Jha and Karl Gruber (f.l.) describe the effects of a DPP3-knockout on the renin-angiotensin system


    For download

    x

    Help

    Search / advanced search of the idw archives
    Combination of search terms

    You can combine search terms with and, or and/or not, e.g. Philo not logy.

    Brackets

    You can use brackets to separate combinations from each other, e.g. (Philo not logy) or (Psycho and logy).

    Phrases

    Coherent groups of words will be located as complete phrases if you put them into quotation marks, e.g. “Federal Republic of Germany”.

    Selection criteria

    You can also use the advanced search without entering search terms. It will then follow the criteria you have selected (e.g. country or subject area).

    If you have not selected any criteria in a given category, the entire category will be searched (e.g. all subject areas or all countries).