Periodic Reporting for period 1 - HeartGenes (Next Generation Gene Therapy for the Treatment of Chronic Myocardial Ischemia and Heart Failure)
Berichtszeitraum: 2021-05-01 bis 2022-10-31
https://www.uef.fi/en/unit/ai-virtanen-institute-for-molecular-sciences
Signaling mechanisms related to angiogenesis have been analyzed in endothelial cells, cardiomyocytes, pericytes and in heart and blood vessels in vivo. We have explored signaling properties of different VEGF-B variants and shown that one of the useful properties of VEGF-B is that it can recruit progenitor cells into the myocardium thus having an important regenerative activity in addition to the angiogenic activity (3). In addition, various non-coding RNAs associated with the activation of VEGF gene expression have been explored.
Electrophysiological mapping using NOGA catheter superimposed on PET radiowater perfusion images were found to be very accurate in the analysis of the effects of intracardiac gene transfers and therefore we have published a detailed description of our large animal ischemia model (4). Also, several modified and regulated vectors have been tested with concomitant perspectives and avenues for future vector development (5) and new nanotherapy delivery methods have been reported (6)
During the grant period two reviews about the potential use of non-coding RNAs and RNAi as drugs for vascular diseases and atherosclerosis have been published (7,8).
I sincerely thank the ERC for the very significant support for our research program.
References:
1. Korpela H, Hätinen O-P, Nieminen T, Mallick R, Toivanen P, Airaksinen J, Valli K, Hakulinen M, Poutiainen P, Nurro J, Yla-Herttuala S. Adenoviral VEGF-B186R127S gene transfer induces angiogenesis and improves perfusion in ischemic heart, iScience 24, 103533, 2021 (https://doi.org/10.1016/j.isci.2021.103533).
2. Korpela H, Lampela J, Airaksinen J, Järveläinen N, Siimes S, Valli K, Nieminen T, Turunen M, Grönman M, Saraste A, Knuuti J, Hakulinen M, Poutiainen P, Kärjä V, Nurro J, Ylä-Herttuala S, AAV2-VEGF-B gene therapy failed to induce angiogenesis in ischemic porcine myocardium due to inflammatory responses. Gene Ther 29:643-652, 2022: (doi:10.1038/s41434-022-00322-9).
3. Mallick R, Gurzeler E, Toivanen PI, Nieminen T, Yla-Herttuala S. Novel Designed Proteolytically Resistant VEGF-B186R127S Promotes Angiogenesis in Mouse Heart by Recruiting Endothelial Progenitor Cells. Front. Bioeng. Biotechnol. 10:1-14, 2022
(doi.org/10.3389/fbioe.2022.907538).
4. Korpela H, Siimes S, Yla-Herttuala S. Large Animal Model for Evaluating the Efficacy of the Gene Therapy in Ischemic Heart. J Vis Exp 175:e62833, 2021 (doi:10.3791/62833).
5. Suoranta T, Laham-Karam N and Ylä-Herttuala S. Strategies to improve safety profile of AAV vectors. Front. Mol. Med. 2:1054069, 2022 (doi: 10.3389/fmmed.2022.1054069).
6. Babu M, Devi D, Mäkinen P, Örd T, Aavik E, Kaikkonen M, Ylä-Herttuala S. ApoA-I Nanotherapy Rescues Postischemic Vascular Maladaptation by Modulating Endothelial Cell and Macrophage Phenotypes in Type 2 Diabetic Mice. Arterioscl. Thromb. Vasc. Biol. 43: 2023 (doi:10.1161/ATVBAHA.122.318196).
7. Ruotsalainen A-K, Mäkinen P, Ylä-Hertuala S. Novel RNAi-based therapies for atherosclerosis. Curr Atheroscler Reports 23:45-50, 2021 (doi: 10.1007/s11883-021-00938-z).
8. Kettunen S, Ruotsalainen A-K, Yla-Herttuala S. RNA interference-based therapies for the control of atherosclerosis risk factors. Curr Opin Cardiol 37: 364-371, 2022 (doi:10.1097/HCO.0000000000000972).